MAZISHI YA MANDELA YAVUNJA REKODI

Nelson Mandela.PICHA|MAKTABA 

Na Mwandishi wetu,mwananchi

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Afrika na dunia inatarajiwa kushuhudia kitu kipya katika maziko ya Rais wa zamani wa Afrika Kusini, Nelson Mandela (95) aliyefariki dunia juzi, baada ya kuugua kwa zaidi ya miezi sita.

Serikali ya Afrika Kusini imesema kiongozi huyo ambaye atazikwa Desemba 15, imeandaa mazishi ya kihistoria yanayosemekana yatazidi yale ya Papa John 11.

Matukio ya shughuli mbalimbali zinazohusu mipango ya maziko ya kiongozi huyo maarufu yanatarajiwa kushuhudiwa sehemu mbalimbali duniani, tofauti na tukio jingine lililowahi kutokea barani Afrika mbali na kombe la dunia.

Rais Jacob Zuma alisema jana kwamba “Mpendwa wetu Madiba atazikwa kwa heshima zote za Serikali. Nimeagiza bendera zote za Afrika Kusini zipepee nusu mlingoti na hiyo itaendelea hivyo hadi tutakapokamilisha mazishi yake.

Mazishi ya Mandela yanalinganishwa na yale ya Papa John Paul II mwaka 2005, ambayo yalihudhuriwa na wafalme watano, malkia sita wa falme mbalimbali na marais wapatao 70 na mawaziri kadhaa, wakiwamo wafuasi wake zaidi ya milioni mbili. Yanakadiriwa pia kulingana na maziko ya Winston Churchil aliyekuwa Waziri Mkuu wa Uingereza mwaka 1965.

Marais wote wa Marekani walio hai wanatarajiwa kuhudhuria mazishi hayo iwapo afya zao zitawaruhusu kusafiri, pamoja na Prince Charles wa Uingereza na hata Rais Robert Mugabe wa Zimbabwe. Pia watu maarufu wenye urafiki wa karibu na Mandela akiwamo msanii Oprah Winfrey wameshathibitisha kuhudhuria.

Changamoto la kiusalama

Kutokana na idadi kubwa ya wakuu wa nchi na watu maarufu duniani wanaotarajiwa kufika Afrika Kusini, suala la usalama limeelezewa kuwa changamoto mpya kwa vyombo vya usalama nchini humo.

Afrika Kusini imekuwa moja ya nchi zinazokabiliwa na matukio ya uporaji na mauaji yanayotokana na idadi kubwa ya wahalifu, wengi wao wakidaiwa kuwa wahamiaji haramu.

“Huyu ni shujaa wa dunia. Tutafanya mipango ya mazishi makubwa ambayo hayajawahi kushuhudiwa. Nadhani kila nchi itakuwa imeandaa utaratibu wake wa namna ya kushiriki,” alisema mmoja wa wanadiplomasia wa Afrika Kusini ambaye hakutaka kutajwa jina lake.

Siku 11 za maombolezo

Serikali ya Afrika Kusini, kwa mujibu wa gazeti la The Guardian tayari imeweka wazi ratiba ya siku 11 za maombolezo tangu alipofariki dunia juzi jioni. Japokuwa ratiba hiyo ilishaandaliwa karibu mwaka mmoja uliopita na kupitiwa na kufanyiwa maboresho katika baadhi ya maeneo, inaonyesha namna maofisa wa Serikali ya Afrika Kusini walivyolipa uzito suala hilo na kulifanya kuwa tukio la kukumbukwa katika historia.
Mwannchi

romanshao: MAISHA YA MANDELA!

romanshao: MAISHA YA MANDELA!: Na. M. M. Mwanakijiji Mpigania haki za weusi na alama kuu ya udhalimu wa mfumo wa Ubaguzi wa Rangi nchini Afrika ya Kusini Mzee Nelson ‘Ma...

READ HERE HOW MEN'S BRAIN ARE WIRED DIFFERENTLY THAN WOMEN'S

Male brains have more connections within hemispheres to optimize motor skills, whereas female brains are more connected between hemispheres to combine analytical and intuitive thinking

By Tanya Lewis and LiveScience

 

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Brain networks showing significantly increased intra-hemispheric connectivity in males (Upper) and inter-hemispheric connectivity in females (Lower). Intra-hemispheric connections are shown in blue, and inter- hemispheric connections are shownImage: agini Verma et al, University of Pennsylvania

Men aren't from Mars and women aren't from Venus, but their brains really are wired differently, a new study suggests.

The research, which involved imaging the brains of nearly 1,000 adolescents, found that male brains had more connections within hemispheres, whereas female brainswere more connected between hemispheres. The results, which apply to the population as a whole and not individuals, suggest that male brains may be optimized for motor skills, and female brains may be optimized for combining analytical and intuitive thinking.

"On average, men connect front to back [parts of the brain] more strongly than women," whereas "women have stronger connections left to right," said study leader Ragini Verma, an associate professor of radiology at the University of Pennsylvania medical school. But Verma cautioned against making sweeping generalizations about men and women based on the results.

Previous studies have found behavioral differences between men and women. For example, women may have better verbal memory and social cognition, whereas men may have better motor and spatial skills, on average. Brain imaging studies have shown that women have a higher percentage of gray matter, the computational tissue of the brain, while men have a higher percentage of white matter, the connective cables of the brain. But few studies have shown that men's and women's brains areconnected differently.

In the study, researchers scanned the brains of 949 young people ages 8 to 22 (428 males and 521 females), using a form of magnetic resonance imaging (MRI) known as diffusion tensor imaging, which maps the diffusion of water molecules within brain tissue. The researchers analyzed the participants as a single group, and as three separate groups split up by age.

As a whole, the young men had stronger connections within cerebral hemispheres while the young women had stronger connections between hemispheres, the study, detailed today (Dec. 2) in the journal Proceedings of the National Academy of Sciences, found. However, the cerebellum, a part of the brain below the cerebrum that plays a role in coordinating muscle movement, showed the opposite pattern, with males having stronger connections between hemispheres.

Roughly speaking, the back of the brain handles perception and the front of the brain handles action; the left hemisphere of the brain is the seat of logical thinking, while the right side of the brain begets intuitive thinking. The findings lend support to the view that males may excel at motor skills, while women may be better at integrating analysis and intuitive thinking.

"It is fascinating that we can see some of functional differences in men and women structurally," Verma told LiveScience. However, the results do not apply to individual men and women, she said. "Every individual could have part of both men and women in them," she said, referring to the connectivity patterns her team observed.

When the researchers compared the young people by age group, they saw the most pronounced brain differences among adolescents (13.4 to 17 years old), suggesting the sexes begin to diverge in the teen years. Males and females showed the greatest differences in inter-hemisphere brain connectivity during this time, with females having more connections between hemispheres primarily in the frontal lobe. These differences got smaller with age, with older females showing more widely distributed connections throughout the brain rather than just in the frontal lobe.

MAISHA YA MANDELA!

Na. M. M. Mwanakijiji

Mpigania haki za weusi na alama kuu ya udhalimu wa mfumo wa Ubaguzi wa Rangi nchini Afrika ya Kusini Mzee Nelson ‘Madiba’ Mandela amefariki dunia baada yakuugua kwa muda mrefu kufuatia maambukizi ya mapafu kushindwa kutengemaa kwa muda sasa. Mzee Mandela ambaye kwa miezi kadhaa sasa amekuwa akisumbuliwa na matatizo ya maambukizi kwenye mapafu yake amefariki dunia nyumbani kwake ambako alipelekewa toka hospitali ya Moyo ya Mediclinic mjini Pretoria, chini Afrika ya Kusini baada ya familia yake kuomba kufanya hivyo.

Nelson Mandela akiwa na Walter Sisulu gerezeni katika Kisiwa cha Robben, Cape Town.

Mzee Mandela alipelekwa hospitali hiyo Jumamosi ya tarehe 8 Juni ikiwa ni baada ya kuanza tena kusumbuliwa na mapafu; miaka ya themanini akiwa kifungoni Mandela alipata ugonjwa wa Kifua Kifuu (TB) kutokana na kazi ngumu ya kupasua mawe kama sehemu ya adhabu ya kifungo chake. Aliondoka hospitali hapo Septemba 1, 2012 baada ya familia kuomba hivyo na kuahidiwa huduma nzuri ya kitabibu nyumbani. Wakati anaondoka hospitali hali yake bado ilikuwa ya utulivu kidogo lakini isiyo na mabadiliko makubwa. Mipango ya mazishi ambayo inatarajiwa kuvuta maelfu ya watu na mamia ya viongozi wa kimataifa inatarajiwa kutangazwa punde.
Bw. Mandela (95) alikuwa Rais wa kwanza mweusi wa Afrika ya Kusini kufuatia kutokomezwa kwa utawala wa ubaguzi wa rangi uliofanywa na Makaburu kwa karibu miaka 400 ambapo watu weupe walijipa haki ya kuwatawala na kuwabagua watu weusi. Kabla ya kuwa Rais wa Afrika ya Kusini Mzee Mandela alitumikia kifungo cha miaka 27 jela ambako pamoja na kazi ngumu aliendelea kuongoza kundi la wapigania haki wengine kudai usawa, utu, na umoja wa Waafrika ya Kusini. Mandela alikuwa ni mfungwa maarufu zaidi wa kisiasa duniani ambapo harakati za kutaka afunguliwe zilipiganwa na wanaharakati sehemu mbalimbali duniani licha ya upinzani wa Serikali ya Afrika ya Kusini na Baadhi ya Nchi za Kimagharibi ambazo zilimuona Mandela kama Ghaidi na mchochezi.
Maisha yake ya awali
Mzee Mandela alizaliwa Julai 18, 1918 katika kijiji cha Mvezo mji mdogo wa Umtatu Jimbo la Cape. Akiwa ni mmoja wa watoto wa Mzee Gadla Henry Mphakanyiswa Nelson Mandela alikulia kwa mamake – mke wa tatu wa Mzee Gadla – katika kijiji cha Qunu ambako pamoja na shughuli nyingine za nyumbani alikuwa mvulana mchunga ng’ombe.

Baadaye alianza masomo ya shule ya msingi na baadaye Sekondari ambapo aliamini kuwa alikuwa anaandaliwa kwa ajili ya utumishi katika nyumba ya Chifu wa Kabila lake la Xhosa kama mshauri. Hata hivyo baada ya kurudi nyumbani kutoka masomoni mwaka 1940 alikuta kuwa Chifu Jongintaba ameandaa ndoa Nelson Mandela pamoja mtoto wa kiume wa Chifu huyo aitwaye Justice walitoroka nyumbani na kwenda kwenye Jiji la Johannesburg. Alifanya kazi kama mlinzi katika Kampuni ya Madini ya Crown lakini alifukuzwa kazi na msimamizi wa pale baada ya kugunduliwa kuwa alikuwa ametoroka kwao.

Mandela akiwa amevaa mavazi ya kabila lake la Xhosa; alitoka katika familia ya kichifu.

Kuingia Katika Siasa

Alipokuwa akiishi kwa muda na mmoja wa binamu zake Nelson Mandela alitambulishwa kwa mwanaharakati wa chama cha ANC Bw. Walter Sisulu ambaye baadaye walifungwa pamoja – Sisulu akitumikia miaka 25 jela. Walter Sisulu alimtafutia kazi ya ukarani katika kampuni ya Wanasheria ya Witkin, Sidelsky and Edelman. Akiwa hapo alifanya masomo ya elimu kwa njia ya Posta ambapo alikuwa anatafuta shahada yake ya kwanza. Mwaka 1943 alihitimu masomo yake ya sheria na kuanza kazi kama Mwanasheria badala ya kurudi kijijini kutumika kwa Chifu. Akiwa ameanza kazi kama Mwanasheria Mandela aliendelea kuwa chini ya uangalizi wa Walter Sisulu ambaye alikuwa anaendeleza harakati za kudai haki za weusi. Akikutana mara kwa mara na wanaharakati wengine nyumbani kwa Sisulu Mandela alikutana tena na rafiki yake Oliver Tambo. Ilikuwa ni katika mikutano hiyo alikutana na mwanamama Evelyn Mase ambaye walianza uhusiano wa mapenzi na baadaye kufunga ndoa yake ya kwanza Oktoba , 1944. Walijaliwa watoto wawili wa kiume na wa kike; wa kiume Madiba “Thembi” Thembikile alizaliwa Februari 1946 na wa kike Makaziwe alizaliwa mwaka uliofuatia lakini alifariki miezi tisa baadaye baada ya kupata maambukizi ya ugonjwa uti wa mgongo.

Mandela na mtoto wake wa kwanza wa kiume Themi.

Baada ya uchaguzi wa 1948 ambapo watu weupe peke yao walishirikia vyama vya Herenigle Nacionale Party na Afrikaner Party viliungana na kuunda chama cha National Party ambacho kilikuwa na sera ya wazi ya ubaguzi na kikapisha na kupanua ukali wa sera ya ubaguzi kupitia sheria mbalimbali za ubaguzi wa rangi. Serikali ya Kikaburu ikaja na mojawapo ya Sheria kali kabisa za kupambana na wanaharakati ambayo inajulikana kama Ukandamizaji wa Ukomunisti ya 1950. Sheria hii ilikuwa inashughulikia karibu mambo yote yanayohusiana na kuipinga serikali na ikiwahusu watu wote. Migongano kati ya ANC na Serikali ya Kikaburu ilianza kupamba moto.

Mwaka 1952 Nelson Mandela alikamatwa na utawala wa Makaburu kwa kile kilichodaiwa kujihusisha na vitendo vya Kikomunisti chini ya ile sheria iliyopitishwa miaka michache nyume. Alihukumiwa miezi tisa jela na “kazi ngumu” lakini utekelezaji wa hukumu hiyo ulisitishwa kwa miaka miwili. Lakini mwezi Disemba mwaka huo huo Mandela alipigwa marufuku kuzungumza na zaidi ya mtu mmoja kwa miezi sita. Akiwa kiongozi wa ANC hii ilimaanisha kuwa asingeweza kufanya mikutano na wanachama wake. Mwaka 1953 Mandela na rafiki yake Oliver Tambo walifungua kampuni yao ya Wanasheria katika Jiji la Johannesburg na kuifanya kuwa kampuni ya kwanza ya Wanasheria Weusi katika Afrika ya Kusini.
Walijishughulisha na malalamiko mbalimbali ya wananchi hasa yanayohusiana na ukatili wa kisiasa. Hata hivyo serikali ikitumia sheria nyingine ikalazimisha kufungwa kwa ofisi hiyo iliyokuwa na wateja wengi na kuihamisha sehemu nyingine ambapo ilikuwa ni vigumu kwa wateja kuifikia. Mwaka 1955 Mandela na wenzake walishirikiana kuandaa kongamano kubwa la watu wa Afrika Kusini ambao wanaamini katika taifa moja la watu wamoja japo wanatoka katika makabila na rangi mbalimbali. Katika kongamano hili kulisainiwa kile kinachoaminika kama mojawapo ya nyaraka muhimu kabisa za kutetea usawa na utu wa watu wote ambayo ilijulikana kama Freedom Charter. Kufananisha hii ni sawasawa na Azimio la Uhuru la Marekani au ile nyaraka ya Waingereza ya Magna Carta. Kwa Tanzania tunaweza kufananisha kabisa na Azimio la Arusha. Freedom Charter ilitengeneza ramani ya kujenga taifa la watu walio huru na sawa katika Afrika Kusini.

Nelson Mandela na Oliver Tambo – wanasheria.
Marafiki wawili – miaka mingi toka Kisiwa cha Robben.

Hata hivyo kwa upande wa familia ndoa yake kwa Evelyn ilianza kuwa matatani. Kulikuwa na tuhuma za kukosa uaminifu ambapo alidaiwa kuwa na mahusiano ya mapenzi na baadhi ya kina dada wa ANC. Evelyn alijaribu watengane lakini pamoja na jitihahada mbalimbali za kupatana Nelson Mandela aliamua kupeana talaka na mke wake wa kwanza mwezi Machi 1958. Walikuwa wamejaliwa mtoto mwingine wa kike. Wakati huo wa mchakato wa talaka Nelson Mandela alikuwa ameanza mahusiano na Winnie Madikizela mmoja wa wafanyakazi wa mambo ya kijamii. Walifunga ndoa Mwezi Juni 1958.

Ndoa ya Madiba na Winnie.

Migogoro na utawala wa kikaburu haikukoma. Na Mandela alizidi kuwa na siasa za mrengo wa kushoto. Njia za amani za kupata mabadiliko ya kisiasa zilionekana kutozaa matunda; Mandela na wenzake walianza kuamini katika njia za kimapinduzi na za kutumia silaha. Hili lilimletea matatizo zaidi na watawala wa Kikaburu. Hatimaye Augusti 2, 1962 Nelson Mandela alikamatwa na utawala wa Makaburu na kushtakiwa kwa kuchochea mgomo wa wafanyakazi na kuondoka nchini bila kibali. Mandela alijiwakilishi mwenyewe mbele ya mahakama huku akitumia nafasi hiyo kutoa hutuba motomoto za kisiasa dhidi ya utawala wa kibaguzi wa makaburu. Alikutwa na hatia na kuamuriwa kufungwa miaka mitano jela; wakati anatoka mahakamani mashabiki wake walisimama pembeni na kuimba wimbo wa Mungu Ibariki Afrika (Nkosi Sikeleli Afrika).

Kesi ya Rivonia

Matatizo yake hayakufikia mwisho. Julai 11, 1963 polisi walivamia shamba la Lilliesleaf – mji mdogo wa Rivonia nje ya Johannesburg) ambapo pamoja na vitu mbalimbali waliamini walikuta ushahidi wa kutosha kumhusisha Mandela na mipango ya kuipindua serikali. Mandela na wenzake walitumia shamba hili kama sehemu yao ya kujificha huku Mandela akijifanya ni mtunza bustani. Kesi hii ilikuwa motomoto kwani Mandela na wenzake walishtakiwa kwa makosa manne yakiwa ni ya uhujumu wa miundo mbinu ya nchi (vitendo zaidi ya 200) pamoja na kutaka kupindua serikali; serikali ilikuwa inapendekeza kuwa wakikutwa na hatia basi wahukumiwe kifo. Mashahidi wengi wa serikali waliitwa pamoja na lundo la ushahidi wa picha na nyaraka kuthibitisha mashtaka ya serikali dhidi ya Mandela na
wenzake tisa.

Mara baada ya kuachiliwa mwaka 1990 Mandela alihakikisha anamtembelea rafiki yake mpenzi Oliver Tambo aliyekuwa anapata matibabu Sweden.

Wengine ambao walikuwa pamoja na Mandela ni pamoja na Walter Sisulu na Govan Mbeki (baba yake na Thabo Mbeki aliyemrithi Mandela kama Rais wa Afrika ya Kusini). Ilikuwa ni katika kesi hii ambapo Mandela alitoa mojawapo ya hotuba zinazosifiwa zaidi duniani na ambayo inasomwa na wanafunzi wa siasa sehemu mbalimbali duniani kwani ilielezea falsafa ya kupinga ubaguzi wa rangi. Inafanana sana kimaudhui na barua ya Martin Luther King Jr akiwa katika jela ya Birmingham huko Alabama ambapo alielezea kwanini alikuwa anapinga kubaguliwa na kwanini kila mpenda haki duniani anapaswa kufanya hivyo hivyo. Katika hotuba hii inayojulikana kama “I’m Prepared to Die Speech” Mandela alisema kuwa alikuwa anapigania haki ya watu weusi kuheshimiwa kutokana na utu wao na kuwa wao ni sawa kama binadamu wengine.

Alisema kuwa hapiganii haki ya weusi kuwabagua weupe bali haki ya watu wote kuishi kwa pamoja kama watu wa jamii moja. Mandela alisema “This is the struggle of the African people, inspired by their own suffering and experience. It is a struggle for the right to live. I have cherished the ideal of a democratic and free society, in which all persons live together in harmony and with equal opportunity. It is an ideal which I hope to live for and achieve. But, if needs be, my Lord, it is an ideal for which I am prepared to die”. Yaani, “Haya ni mapambano ya watu wa Afrika yaliyotokana na mateso na mang’amuzi yao wenyewe. Haya ni mapambano ya kupigania haki ya kuishi. Nimelifurahia wazo la jamii ya kidemokrasia na huru, ambapo watu wote wanaishi katika amani na haki sawa. Ni wazo ambalo ninatumaini kuishi kwa ajili yake na kulitimiza. Lakini, ikibidi, mheshimiwa, ni wazo ambalo nimejiandaa kufa kwa ajili yake”.

Baada ya kuhukumiwa kifungo cha maisha Mandela na wenzake wakitoka Mahakamani.

Pamoja na utetezi wake wote timu ya Mandela ilishindwa kesi hii na wote wakakutwa na hatia isipokuwa mmoja. Kwa vile tayari kulikuwa na mwamko sehemu mbalimbali duniani kupinga adhabu ya kifo Mahakama ikawaamuru Mandela na wenzake kutumikia kifungo cha maisha na huo ndio ukawa mwanzo wa kifungo cha karibu miaka 30 jela (ikumbukwe kesi hii ilipoanza Mandela tayari alikuwa anatumikia ile hukumu ya miaka 5 jela). Mandela na wenzake walipelekwa katika jela ya Kisiwa cha Robben ambako pale peke yake alitumikia miaka 18. Maisha kifungoni Kisiwa cha Robben na kwingine.Kisiwa cha Robben ambako Mandela alifungwa kwa miaka 18.

Mandela na wenzake walihukumiwa kazi ngumu vile vile na kweli ilikuwa ni kazi ngumu kwani pamoja na kuponda mawe walipewa baadaye kazi ya kuponda mawe ya chokaa. Kwa muda alikatazwa kuvaa miwani ya jua kitua mbacho kilimsababishia ubovu wa macho ambao hakuweza kupona kabisa. Akiwa kifungoni mamake alimtembelea mwaka 1968 na siku chache baadaye alifariki dunia, mwaka uliofuata mtoto wake wa kwanza Thembi alifariki katika ajali ya gari – Mandela hakuruhiswa kuhudhuria mazishi yao wote hao. Maisha kifungoni yalikuwa magumu kwa kila kipimo licha ya maisha baada ya miaka kuanza kuboreshwa kidogo kufuatia maandamano na harakati za kutaka Mandela afunguliwe. Utawala wa makaburu hawakusikia la mtu yeyote hasa kwa vile walikuwa wanaushirika wa karibu na serikali ya Marekani na Uingereza ambazo zote zilimuona Mandela kama Mkomunisti na Ghaidi.

Mwaka 1966 gerezani Mandela anaonekana akiitia viraka nguo yake ya jela.

Mandela alitumikia pia katika magereza ya Pollsmoor huko Cape Town na Gereza kati ya 1982 hadi 1988 na baadaye gereza la Victor Verster 1988-1990 ambako kwa kiasi kikubwa alikuwa amepewa maisha ya unafuu (hapa chini akiwa na mpishi na huduma mbalimbali) kulinganisha na alivyoishi katika gereza la Kisiwa cha Robben.

Akiwa gereza la Victor Verster alipewa nyumba na mtumishi. Hapa pichani na aliyekuwa mpishi wake kwenye gereza hilo.

Ikumbukwe miaka aliyokuwa Robben ndiyo ilikuwa migumu zaidi kwani hakuruhusiwa kutembelewa na watu wengi na alipewa nafasi ya kutembelewa na kuandikwa barua moja tu kila baada ya miezi sita. Katika magereza hayo mengine Mandela alipata unafuu kidogo.
Kuingia kwa F. W. de Clerk na kuachiliwa kwa Mandela
Chini ya utawala wa Pieter Botha Afrika ya Kusini ilizama katika siasa na sera za ubaguzi wa rangi. Botha aliwachukia weusi na aliamini kabisa kuwa utawala wa kikaburu utadumu kwa muda mrefu. Botha anaweza kabisa kufananishwa na aliyekuwa Gavana wa Alabama George Wallace ambaye aliapa kuwa “ubaguzi sasa, ubaguzi kesho, ubaguzi milele”; japo aliishi na kuona Ubaguzi ukifumuliwa katika jimbo lake na katika Marekani sera hizo zikitupwa katika mifumo ya utawala. Hata hivyo alikuwa ni F. W. de Clerk mwanasiasa mwingine mzungu ambaye licha ya kutoka katika chama kilichoamini katika ubaguzi wa rangi yeye mwenyewe alijikuta akiukataa kifikra kwani aliona hauwezi kudumu.
Kwa muda hivi tangu 1988 Mandela alikuwa na mazungumzo ya siri na baadhi ya viongozi wa serikali juu ya masharti ya yeye na wenzake kuachiwa huru na mwelekeo wa siasa za Afrika ya Kusini. Mazungumzo hayo yalikumbana na vikwazo vingi sana ikiwemo kutokukubaliana kwa masharti – kwa mfano serikali ilitaka Mandela asijiingize kwenye siasa na kuwa wasilazimishwe kuwa na utawala wa wengi (majority rule) masharti ambaye Mandela aliyakataa.

Baada ya Mdahalo mzito ambao de Klerk alionekana kushinda; Mandela alipompa mkono alionekana kushangaza umati wa watu na kujenga daraja kati yake na de Klerk kwa maisha.

Matokeo yake ni kuwa Mandela na wenzake waliachiliwa huru na utawala lwa De Clerk Februari 2, 1990 na kuleta furaha wanaharakati pote duniani. Ikumbukwe kwa Tanzania wimbo maarufu wa “Kilicho cha Wapenda Haki Duniani Kote” ulivuma sana wakati huo katika kuhamasisha Mandela na wenzake waachiliwe huru. Baada ya kuachiliwa huru muda mrefu ulitumika kufanya mazungumzo na utawala wa kikaburu kuhusiana na mwelekeo wa siasa za Afrika ya Kusini na hata kuelekea uchaguzi mkuu. Hata hivyo kutokana na matukio mbalimbali ya vurugu na mauaji ya kisiasa yaliyokuwa yanaendelea na hata migongano ya chama cha Inkatha cha Chifu Buthelezi Mandela aliona hana jinsi isipokuwa kufikia makubaliano ya msingi. Baadhi ya makubaliano hayo yalihusisha kufunguliwa kwa wafungwa wa kisiasa, kuitishwa kwa uchaguzi mkuu, kuwa na Katiba ya Mpito na kuhakikishia kuwa kazi za weupe hazitafukuzwa kama ukiingia utawala wa weusi.Mandela na de Klerk walitunukiwa tuzo ya Nishani ya Amani ya Nobel mwaka 1993 Mandela na de Klerk wakionesha nishani ya Nobel
Uchaguzi Mkuu wa 1994
Hatimaye Afrika ya Kusini ikaingia katika uchaguzi mkuu wa kwanza huru na wawananchi wote mwaka 1994, Aprili 27. Kampeni ilikuwa na vurugu za hapa na pale lakini kwa ujumla wananchi wa Afrika ya Kusini hasa weusi walijikuta kwa mara ya kwanza wanapiga kura kumchagua kiongozi wanayemtaka. Mandela akiongoza ANC walishinda asilimia 62 ya kura na kushindwa kupata theluthi mbili ambayo ingewawezesha kuweza kubadili Katiba. Serikali yake ilikuwa ni ya umoja wa kitaifa ikitegemea kwa kiasi kikubwa baadhi ya maofis waliokuwa katika utawala wa kikaburu. De Clerk alikuwa Makamu wa kwanza wa Rais na Thabo Mbeki akiwa Makamu wa Pili wa Rais. Mandela (katikati) akiwa na Makamu wake wawili
Mandela alishaeleza toka awali kuwa atagombea kipindi kimoja tu na ndivyo alivyofanya na baadaye kumwachia Thabo Mbeki kama Rais wa Afrika ya Kusini. Baada ya kustaafu siasa Mandela aliamua kujishughulisha na program mbalimbali za ndani ya Afrika ya Kusini na kutembelea baadhi ya nchi. Hata hivyo udhaifu wa mwili uliotokana na magonjwa na uzee ulimzidia na kumfanya apunguze safari za nje. Kwa mara ya mwisho alionekana katika shughuli za hadhara katika mashindano ya Kombe la Dunia mwaka 2010 ambayo yalifanyika Nchini Afrika ya Kusini.
Mandela na Tanzania
Tanzania kama nchi imehusika kwa kiasi kikubwa sana katika kuuvunja vunja utawala wa kikaburu na katiak kuongoza harakati za kutaka Mandela aachiliwe huru. Baba wa Taifa Mwalimu Nyerere na utawala wake mara baada ya Uhuru 1961 aliazimia kutoa msaada wote unaohitajika kwa wapigania uhuru wa Afrika ya Kusini. Kama ilivyodokezwa hapo juu kuwa mojawapo ya mashtaka dhidi ya Mandela ni lile la kwenda nje ya Afrika ya Kusini bila kibali. Mwaka 1962 Mandela akitumia njia za panya alitoroka Afrika ya Kusini na hatimaye kuingia Tanganyika na kukutana na Mwalimu Nyerere ambaye aliwapa ahadi ya ushirikiano mkubwa. Mandela mwenyewe akizungumza katika dhifa aliyomwandaliwa Baba wa Taifa Mwalimu Nyerere mwaka 1997 Oktoba 17; alisema “Inanyenyekesha kukumbuka mchango wa Mwalimu Nyerere katika ukombozi wa bara letu na Uhuru wa Afrika ya Kusini”.

Aliendelea na kumsifia Nyerere kwa kusema kuwa wakati watu wengine walikuja baadaye kuona ubaya wa utawala kikaburu Nyerere aliliona hili mwaka 1959 ambapo akishirikiana na Fr. Huddleston walianzisha harakati za kupinga ubaguzi wa rangi (anti-apartheid movement) ambao zilikuja kuwa maarufu sana baadaye – hasa baada ya kesi ya Rivonia. Mandela alisema kukutana na Mwalimu mwaka 1962 kulimuonesha jinsi Nyerere alivyokuwa anataka haki sehemu zote duniani na jinsi alivyojitoa yeye na taifa lake changa kuona kuwa Afrika yote inakuwa huru.

Wanaharakati – wakisherehekea miaka 80 ya Askofu Trevol Huddleston, Nyerere, Askofu Mkuu Desmond Tutu na aliyekuwa Katibu wa Jumuiya ya Madola Shirdath Ramphal.

Katika kuonesha hili Mandela alichagua Tanzania miongoni mwa nchi za kwanza kutembelea mara baada ya kuachiliwa huru mwaka 1990. Aliingia nchini Machi 7, 1990 na kupokelewa na maelfu ya watu wakiongozwa na baba wa Taifa Mwalimu Julius Nyerere pamoja na Rais Ali Hassan Mwinyi. Wakati anatembelea nchini kama mtu huru Tanzania ilikuwa na wapiganaji karibu 10,000 wa Afrika ya Kusini waliokuwa wanaishi Tanzania na kujihusisha na mambo mbalimbali. Ikumbukwe ANC ilifungua ofisi yake ya kwanza nje ya Afrika ya Kusini Jijini Dar-es-Saalam mwaka 1961 na hii ilichangia baadaye pia kwa ofisi za vyama vingine vya ukombozi kuchagua Dar kama makao yao makuu.

Yote haya yalisaidia kuifanya Tanzania kuwa makao makuu ya Kamati ya Ukombozi ya Nchi Zilizo Mstari wa Mbele ambayo kwa muda mrefu iliongozwa na Brig. Hashim Mbita. Uhusiano huu wa karibu wa Tanzania na Wapigania Uhuru ulithibitika zaidi baada ya Tanzania kuwapatia wapigania uhuru hao maeneo ya mafunzo ya kijeshi na taaluma mbalimbali huko Morogoro eneo la Mazimbu na maeneo mengine Mtwara na sehemu nyingine nchini. Pamoja na vyuo wapigania uhuru hao walipewa maeneo ya shule za msingi na sekondari vile vile.

Wakufunzi wa chuo cha ANC Mazimbu Morogoro enzi hizo.

Uhusiano huu wa karibu wa Tanzania na wapigania uhuru wa Afrika ya Kusini ulionekana pia wakati wa Mkutano wa Mawaziri Wakuu wa Nchi za Jumuiya za Madola uliofanyika London, Uingereza . Katika makala yake aliyoandika kwenye gazeti la The Observer Machi 7, 1961 Nyerere aliweka msimamo wa Tanganyika mapema kabisa kuhusiana na uanachama wa Afrika ya Kusini kwenye Jumuiya hiyo (Afrika ya Kusini iliomba kuwa mwanachama na mawaziri wakuu walitakiwa kuchukua uamuzi). Katika makala hiyo Nyerere alisema mojawapo ya mistari inayokumbukwa sana kuwa “kuipigia kura Afrika Kusini ijiunge ni kutupigia kura sisi kujitoa (To vote South Africa in, is to vote us out) na inaaminikuwa kuwa hoja aliyoijenga ilichangia sana kubadili upepo na kusababisha Afrika ya Kusini kutoa ombi lake la kujiunga. Uhusiano wa karibu wa Nyerere na Mandela haukushia wakati huo tu; hata baada ya kifo cha Mwalimu alikuwa ni Nelson Mandela aliyechukua jukumu la kusaidia kuleta amani Rwanda kama Mpatanishi.

Buriani.

Mandela ametutoka baada ya maisha ambayo ametumikia nchi yake, bara lake na dunia kwa namna ambayo ameacha alama ya kudumu ya kukumbukwa. Kwa mtu ambaye utawala wa kikaburu ulimnyima haki nyingi za msingi na kumchukulia miaka ishirini na saba ya maisha yake angeweza kuwa mtu mwenye kisasi pale aliposhika madaraka kama Rais wa nchi yake. Mtu ambaye alinyanyaswa, kuteswa, na kushindwa hata kuhudhuria mazishi ya mamake kwa namna ya kawaida angekuwa ni mtu mwenye kinyongo sana.

Hata hivyo Mandela alionesha huruma na msamaha wa hali ya juu sana. Aliposhika madaraka alihakikisha kuwa watu weupe wanajihisi salama na kuondoa kabisa roho ya kulipiza kisasi hasa kwa watu weusi ambao waliumia sana mikononi mwa weupe kwa karibu miaka 400. Anapoitwa “Baba wa Taifa” la Afrika ya Kusini haitwi hivyo kirahisi. Mchango wake wa pekee kwa nchi yake unamuweka katika nafasi ya pekee kukumbukwa na vizazi vingi vijavyo. Hali hii ya msamaha iligusa hata maisha yake binafsi. Pamoja na kupata habari za mkewe Winnie Mandela kukosa uaminifu Mandela bado alihakikishia kuwa anapatiwa uwakilishi wa kutosha kujitetea kwenye kesi iliyomkabili ya utekaji na mauaji. Hata baada ya kuachana naye Mandela na mkewe mpya Graca Machel – aliyekuwa mke wa marehemu Samora Machel (Rais wa Msumbiji aliyeuawa kwa njama za makaburu) – Mandelea amekuwa na mahusiano mazuri na ya utulivu na Winnie ambaye ameshiriki vilivyo katika kumuuguza Madiba.

Dunia kwa hakika imepoteza shujaa wa haki za binadamu, nyota ya Afrika na mfano wa viongozi ambao waliweka maslahi ya watu wao mbele zaidi kuliko furaha zao binafsi na za familia zao. Wananchi wa Afrika ya Kusini wanapomlilia wanaungana na mamilioni zaidi katika bara la Afrika na Dunia ambao wanakumbuka nafasi ya Mandela katika maisha yao.

Kwa Watanzania wengi hasa waliokua miaka ya sabini na themanini harakati za kutaka Mandela afunguliwe na kukomeshwa kwa utawala wa kikaburu zilikuwa ni sehemu ya maisha yao. Hawa pia wanamshukuru Mungu kwa maisha ya Mandela na wanaungana kutoa rambirambi na pole kwa familia ya Mandela na kumwombea pumziko la amani baada ya maisha ya uchovu na kazi ngumu. Watanzania wanaungana na ndugu zao wa Afrika ya Kusini katika maombolezo haya; wao wenyewe wanakumbuka vile vile jinsi walivyoondokewa na Baba wa Taifa Mwalimu Nyerere na jinsi akili ya jumla ya Taifa ilivyoguswa lakini pia kuonekana kwa kubadilika kwa taifa kwa kutokuwepo Mwalimu. Ni wazi kuwa hata Afrika ya Kusini nayo itapita huku ambapo ile Dhamira ya Taifa (Consciousness of a Nation) yaani Mandela atakuwa hayupo. Njia pekee ya kuhakikisha kuwa Afrika ya Kusini inazidi kujijenga katika maisha ya kisasa na kuinua watu wake kuelekea maendeleo ni lazima kukumbuka umoja na udugu ambao Mandela alipigania.

MUNGU AILAZE ROHO YAKE MAHALA PEMA PEPONI

How To Prevents Obesity, Cancers, Fibroids, Hepatitis: Health is Wealth

How To Prevents Obesity, Cancers, Fibroids, Hepatitis: Health is Wealth: Environmen tal Health Products That Prevents Obesity, Cancers, Fibroids, Hepatitis, Help to Boost the Immunity of people with HIV ...

AL SHABAAB WAFANYA SHAMBULIZI LA KUSHTUKIZA MWANZA.

YALIYOKEA WESTGATE, SASA YATOKEA MWANZA NDANI YA GOLD CREST HOTEL. WANANCHI MWANZA WABAKI NA TAHARUKI. TAZAMA PICHA HAPA

Ikiwa ni mwezi mmoja na siku kadhaa zimepita tangu kutokea kwa tukio la kigaidi la uvamizi wa maduka ya Westgate mjini Nairobi yaliyofanywa na kundi la wanamgambo wa al-Shabaab, asubuhi ya leo ya Novemba 7 2013, mamlaka za usalama Mkoani Mwanza zimefanya uvamizi kwenye hoteli ya Gold Crest ya jijini Mwanza.

Uvamizi huo ambao kwa taarifa za awali kutoka katika vyanzo vyetu lilikuwa ni la jaribio kuona uwezo na namna ya wananchi na jamii kwa ujumla wanavyoweza kukabiliana na matukio ya aina hiyo.

Hata hivyo tukio hilo lililochukua muda wa saa nzima limeibua takaruki kwa wananchi waliokuwa ndani ya hoteli na nje ya hoteli hiyo jambo lililopelekea umati wa watu wengi kukusanyika kwa lengo la kujua nini kinachoendelea.

Hakika kwa utamaduni huu wa watanzania kukimbilia kwenye eneo la tukio badala ya kukimbia sehemu salama kuna hatari ya watu wengi kupoteza maisha kama tukio kama hili likitokea katika mazingira ya uhalisia (tunaomba manani atuepushe na mabalaa ya namna hii). Tazama picha zote za tukio hili lakini nitoe angaliazo tu kuwa TUKIO HILI NI LA MAJARIBIO NA LIMEFANYWA KWA KUSHTUKIZA.

bacteriology. endotoxins

BACTERIAL TOXINS

Bacterial toxins are exotoxins and endotoxins. Characteristics and differences of exotoxins and endotoxin are listed in down the page.

EXOTOXINS
Exotoxin producing bacteria

1.   Corynebacterium diphtheriae. Strains that carry a temperate bacteriophage are toxigenic causes diphtheria. Exotoxin inhibits protein synthesis and causes cell death. Causes diphtheria.

2.   Clostridium tetani. Exotoxin blocks action of inhibitory neurones of spinal cord. Causes tetanus.

3.   Clostridium perfringens. (a) Causes gas gangrene. Exotoxin (alpha toxin) has lacithinase activity and thereby causes cell death, (b) Enterotoxin causes hyper secretion of water and electrolytes in diarrhoea.

4.     Clostridium botulinum. Exotoxin causes paralysis of deglutination and respiratory muscles. It blocks release of acetylcholine of synapses and neuromuscular junctions. Causes botulism.

5.   Vibrio cholerae 01 and 0139. Enterotoxin (Exotoxin) causes hyper secretion of water and electrolytes within gut in diarrhoea.

6.   Enterotoxigenic E. coll. Produce enterotoxin (LT- heat labile exotoxin) causes hypersecretion of water and electrolytes within gut.

7.   Shigella dysenteriae type 1 (Shiga bacillus). Exotoxin causes acute inflammation.

8.   Staphylococcus aureus- some strains : (a) Toxic shock syndrome toxin-1. Causes toxic shock syndrome. (b) Staphylococcal enterotoxin causes toxin type food poisoning and stimulates vomiting centre of brain.

9.   Streptococcus pyogenes. Pyrogenic (Erythrogenic) exotoxin causes scarlet fever and toxic shock syndrome.

NOTE : Enterotoxins are exotoxins that are associated with diarrhoea) diseases and food poisoning. Bacteria producing enterotoxins are V. cholerae, enterotoxigenic E. coli (ETEC), some strains of S. aureus, V. parahaemolyticus, Y. enterocolitica, Aeromonas species, and C. perfringens.

Toxoid. Toxoid is modified exotoxin. An exotoxin has two main properties : 
(1) toxicity, and
(2) antigenicity. In toxoid, the toxicity of the toxin is destroyed but its antigenicity is preserved. As such toxoids e.g. diphtheria toxoid, tetanus toxoid can be safely used for vaccines. Toxins can be converted to toxoid by different methods e.g. formalin treatment.

ENDOTOXINS

Endotoxins are the integral part of the cell walls of Gram-negative bacteria, and are liberated when bacteria are disintegrated (lysed). Cell wall of Gram negative bacteria contain lipopolysaccharides (LPS, endotoxin) which consists of : (1) Lipid A. This is the endotoxin and is the core, and (2) Polysaccharide form coat. This is the 0 antigen which can induce specific immunity. Physiological, pathological and clinical effects of endotoxins of different Gram negative bacteria are similar. These are :

1. Fever. The endotoxin acts on mononuclear phagocytes (monocytes/macrophages), with liberation of interleukin-1 (endogenous pyrogen). Interleukin-1 acts on thermoregulatory centre. Chill is due to widespread arteriolar and venular constriction.
2. Leucopenia occurs early with onset of fever. It may be followed by leucocytosis.

3. Hypoglycaemia. LPS enhances glycolysis in many cell types and can lead to hypoglycaemia.

4.  Hypotension occurs early in Gram-negative bacteraemia.

5.  Shock. 'Endotoxic' or 'septic' shock may develop in severe Gram-negative bacteraemia (See chapter 4).

6.      Activation of complement. Endotoxin activates complement system by alternative pathway.

7.  Disseminated Intravascular Coagulation (DIC). DIC may occur in Gram negative bacteraemia. It is initiated on activation of factor XII (Hageman factor) of coagulation cascade by endotoxin which finally leads to conversion of fibrinogen to fibrin. Endotoxin leads platelets to adhere on vascular endothelium. Endotoxin can activate plasminogen to plasmin which acts on fibrin producing fibrin-split products. Shwartzman phenomenon is taken as a specialized form of DIC.

8.  Death may occur due to shock and/or DIC.

NOTE: Peptidoglycan of Gram-positive Bacteria: Peptidoglycan of Gram-positive bacteria released during infection may produce similar activities as LPS of Gram-negative bacteria. However, peptidoglycan is much less potent than LPS.

Characteristics and Differences of Exotoxins and Endotoxins

Endotoxin:
1.   Integral part of the cell wall of Gram-negative bacteria. Released on bacterial death and in part during growth. Release is not required for biologic activity.
2.   Formed only by Gram-negative bacteria
3.   Lipopolysaccharides. Lipid A portion is responsible for toxicity.
4.   No specific receptor.
5.   Moderately toxic. Fatal to animals in large doses.
6.   Relatively heat stable. Toxicity is not destroyed above 60°C for hours.
7.   Weakly antigenic. Antibodies are protective.
8.   Not converted to toxoid.
9.   Synthesis directed by chromosomal genes.
10.  Usually produce fever in the host by release of interleukin-1 and other mediators..]

Exotoxins:
1.Excreted by living cells
2.   Produced by Gram-positive and Gram-negative bacteria
3.   Polypeptides
4.   Usually bind to specific receptors on cells
5.   Highly toxic. Fatal to animals in very small doses
6.   Relatively heat labile. Toxicity destroyed over 60°C
7.   Highly antigenic. Stimulate formation of antitoxin. Antitoxin neutralizes the toxin
8.   Converted to toxoid by formalin. Toxoid is nontoxic but antigenic. Toxoids are used to immunize, e.g. tetanus toxoid
9.   Usually controlled by extra-chromosomal genes, e.g. plasmids, phage gene
10.  Usually do not produce fever in the host.

GENETIC ELEMENTS

Nucleoid- Bacterial Chromosome

Bacterial nucleoid consists of a single circular molecule. It is a single, haploid chromosome of about 1 mm long in unfolded state. Bacterial chromosome (DNA) is attached to a septa) mesosome. Nucleoids consist of DNA, smaller amounts of RNA, RNA polymerase and probably other proteins. The nucleoid replicates by fission. It has no nucleolus, nuclear membrane, spindle or non-identical chromosomes. Genes of the nucleus determines the amino acid sequences and hence the structure of a protein and thereby all the properties of the organism. These account for heredity. Recently it has been found that some prokaryotes have a linear chromosome. Staining of Nucleus. Nuclei are stained with Feulgan stain which is specific for DNA.


Plasmid
Certain bacteria contain plasmid. These are extra-chromosomal genetic material (DNA), ie. genetic determinant, and are mostly circular. Certain properties are determined by plasmid:

1.Virulence factors, eg. In enteropathogenic E. coli strains, both enterotoxins and colonization antigens (pill). Other exotoxin productions are frequently controlled by plasmids.

2.Drug resistance by R factors (Resistance plasmids).

3.Metabolic activities may be determined. Examples: Sucrose uptake and metabolism, and citrate uptake by Escherichia coli.

4.Production of colicins (Bacteriocins) by many Gram-negative bacteria is controlled by plasmids.

5.Transfer of genetic material by sex factors (See Chap. 40).


Transposon
Transposons are genetic elements with DNA sequences


CYTOPLASMIC STRUCTURES
Mitochondria are absent in prokaryotic cells.

1. Ribosomes. They are present as minute granules in large number. RNA is the principal component of ribosomes.

2. Nutrient granules. These are not essential or permanent structures: These may be:

(a)Metachromatic, Volutin or Babes-Ernst granules. These may be present in Corynebacterium diphtheriae and may be used for identification. These act as reserve of energy. These have affinity for basic dyes. Albert staining is done to demonstrate metachromatic granules.
(b)Lipid granules. These are P- hyd roxybu rate.
(c)Polysaccharide granules, eg. glycogen, starch.
(d)Other granules, eg. sulphur.

3. Carotenoids- Photosynthetic pigments are present in photosynthetic bacteria.

FLAGELLA

A large number of bacteria possess flagella. Flagellum is the organ of locomotion. Flagellated bacteria are motile. Nonflagellated bacteria are non-motile.

Examples:
Motile Bacteria: Escherichia, Salmonella, Proteus, Pseudomonas, Vibrio, Aeromonas, Plesiomonas, Campylo­bacter, Helicobacter, Clostridium tetani.

Nonmotile Bacteria: All Cocci, Shigella, Klebsiella, Corynebacterium diphtheriae, Clostridium perfringens, Bacillus anthraces, Haemophilus, Bordetella, Brucella, Yersinia, Pasteurella, Francisella.

Structure . Flagella are long, slender thread-like (12-30 nm in diameter) organs of locomotion. A flagellum is attached to the bacterial cell body by a complex structure consisting of filament, hook and basal body. The basal body has one pair of rings in Gram-positive bacteria and two pairs in Gram-negative bacteria. A bacterial flagellum is composed entirely of protein. A flagellum is made up of several thousand molecules of a protein subunit called flagellin. The flagellum is formed by the aggregation of subunits to form a helical structure.

A flagellated bacterium may become non-flagellated but not the reverse. The arrangement of flagella for a particular bacterium is constant and is one of the four types.

1.   Peritrichous. Flagella are distributed over the entire cell, e.g. Escherichia coli, Salmonella genus.

2.   Amphitrichous. There is a single flagellum at each pole.

3.   Lophotrichous. There is a bunch of flagella at one or both poles, e.g. Spirillum minus.

4.   Monotrichous. There is a single polar flagellum at one pole, e.g. Vibrio cholerae.

They have no function in the virulence of the bacteria. Antigenic structure of the flagella (H antigens) may be used for identification and classification of bacteria.

Sensory transduction is the behavior of the flagellated bacteria in response to the environment. This may be: (1) Chemo taxis is the movement of the bacterium towards a chemical attractant, e.g. sugar, amino-acid, (2) Aerotaxis­movement towards the optimal oxygen concentration, (3) Electron acceptor taxis- movement towards alternative electron receptors, (4) Photo taxis- movement towards light of photosynthetic bacteria.

Motility Test. Hanging-drop preparation is done by placing a drop of bacterial suspension between a slide and cover slip separated by a circular layer of Vaseline on the surface of the slide.

Flagella Staining. They are demonstrated by special staining. Flagella are not visible under light microscope. Bacteria are first treated with tannic acid salt which precipitates on flagella and cell walls and increases the diameter of the flagella. They are then visible under light microscope.

PILI (FIMBRIAE)

Pill or fimbriae are very thin, hair-like short rigid surface appendages. Many Gram-negative bacteria possess pili or fimbriae. There may be 100-500 pili in one cell. They are shorter and finer than flagella and composed of protein subunits termed pilins. Minor proteins, located at the tips of pili, are responsible for the attachment properties. They are seen by electron microscope. Pellicle formation in the fluid media by bacteria is due to fimbriae. Pill of different bacteria are antigenic ally distinct. Some bacteria, e.g. N. gonorrhea are able to make pili of different antigenic types (antigenic variation) and this can still adhere to cells by a type in presence of antibodies to other types. Fimbriae of group a streptococci are the site of the surface antigen, M protein. Lipoteichoic acid, associated with these fimbriae is responsible for adherence of these streptococci to epithelial cells of the hosts. There are two types of pili on function:

1. Ordinary pill. These play roles in adherence of bacteria to host cell surfaces. 'Colonization antigens' are ordinary pili that provide the cells with adherent properties, genetically determined by plasmids.

2.   Sex pill. These give the 'maleness'. They are few in number and very long, e.g. in enter bacteria. During bacterial conjugation the male (donor) cell adhere with its sex pili and transfer DNA to non-male (recipient) cell. The pili act as conjugation tubes. In this way the genetic material which determines antibiotic resistance may pass from one bacterium to another. Sex pili possess receptors to which bacteriophage can become attached.

BACTERIAL SPORES (ENDOSPORES)

Bacterial endospores are formed when conditions for vegetative growth are not favorable.


Spore-Forming Bacteria
1.Bacillus and Clostridium genera form spores.
2.   Sporosarcina (Gram-positive coccus) and possibly Coxiella burnetii can produce spores.


Demonstration of Spore:
1.In Gram stain, the spore appears as unstained colorless areas in cells.
2. Spores are stained with malachite green, or carbol fuchsin (by modified Ziehl-Neelsen stain).

Nature. The spore is a resting cell. Spores are in a subdued metabolic state and non-reproducing. Each cell forms a single internal spore that is liberated when the mother cell undergoes autolysis. The spore is highly resistant to heat, chemical agents and desiccation. In sporulation, each vegetative cell forms only one spore, and in subsequent germination each spore gives rise to a single vegetative cell.

BACTERIAL GROWTH

Growth of Bacteria is the orderly increase of all the chemical constituents of the bacteria. Multiplication is the consequence of growth. Death of bacteria is the irreversible loss of ability to reproduce.

Bacteria are composed of proteins, carbohydrates, lipids, water and trace elements.


Factors Required for Bacterial Growth
The requirements for bacterial growth are:
(A)) Environmental factors affecting growth, and
(B) Sources of metabolic energy.

A. Environmental Factors affecting Growth
1. Nutrients. Nutrients in growth media must contain all the elements necessary for the synthesis of new organisms. In general the following must be provided : (a) Hydrogen donors and acceptors, (b) Carbon source, (c) Nitrogen source, (d) Minerals : sulphur and phosphorus, (e) Growth factors: amino acids, purines, pyrimidines; vitamins, (f) Trace elements: Mg, Fe, Mn.

Growth Factors: A growth factor is an organic compound which a cell must contain in order to grow but which it is unable to synthesize. These substances are essential for the organism and are to be supplied as nutrients. Thiamine, nicotinic acid, folic acid and para-aminobenzoic acid are examples of growth factors.

Essential Metabolites: These metabolites are essential for growth of bacterium. These must be synthesized by the bacterium, or be provided in the medium. Mg, Fe and Mn are essential trace elements.

Autotrophs live only on inorganic substances, i.e. do not require organic nutrients for growth. They are not of medical importance.

Heterotrophs require organic materials for growth, e.g. proteins, carbohydrates, lipids as source of energy. All bacteria of medical importance belong to heterotrophs. Parasites may depend on the host for certain foods. Saprophytes grow, on dead organic matter.

2.   pH of the medium. Most pathogenic bacteria grow best in pH 7.2-7.4. Vibno cholerae can grow in pH 8.2-9.0

3.   Gaseous Requirement
(a) Role of Oxygen. Bacteria may be classified into four groups on oxygen requirement :
(i)    Aerobes. They cannot grow without oxygen, e.g. Mycobacterium tuberculosis.
(ii)   Facultative anaerobes. These grow under both aerobic and anaerobic conditions. Most bacteria are facultative anaerobes, e.g. Enterobacteriaceae.
(iii)Anaerobes. They only grow in absence of free oxygen, e.g. Clostridium, Bacteroides.
(iv)   Microaerophils grow best in oxygen less than that present in the air, e.g. Campylobacter.

Aerobes and facultative anaerobes have the metabolic systems: (1) cytochrome systems for the metabolism of oxygen, (2) Superoxide dismutase, (3) catalase.

Anaerobic bacteria do not grow in the presence of oxygen. They do not use oxygen for growth and metabolism but obtain their energy from fermentation reactions. Anaerobic bacteria are killed by oxygen or toxic oxygen radicals. Multiple mechanisms play role for oxygen toxicity : (1) They do not have cytochrome systems for oxygen metabolism, (2) They may have low levels of superoxide dismutase, and (3) They may or may not have catalase.

(b) Carbon dioxide. All bacteria require CO2 for their growth. Most bacteria produce CO2. N. gonorrhoeae and N. meningitides and Br abortus grow better in presence of 5 per cent CO2.

4.   Temperature. Most bacteria are mesophilic. Mesophilic bacteria grow best at 30-37°C. Optimum temperature for growth of common pathogenic bacteria is 37°C. Bacteria of a species will not grow but may remain alive at a maximum and a minimum temperature.

5.   Ionic strength and osmotic pressure.

6.   Light. Optimum condition for growth is darkness. 


B.Sources of Metabolic Energy
Mainly three mechanisms generate metabolic energy. These are fermentation, respiration and photosynthesis. An organism to grow, at least one of these mechanisms must be used.

REPRODUCTION
Bacteria reproduce by binary fission. Multiplication takes place in geometric progression. The nucleus (chromosome) undergoes duplication prior to cell division. When the cell grows about twice its size, the nuclear material divides, and a transverse septum originates from plasma membrane and cell wall and divides the cell into two parts. The two daughter cells receive an identical set of chromosomes. The daughter cells separate and may be arranged singly, in pairs, clumps, or chains.

GROWTH CURVE
The growth curve indicates multiplication and death of bacteria. When a bacterium is inoculated in a medium, it passes through four growth phases which will be evident in a growth curve drawn by plotting the logarithm of the number of bacteria against time. Number of bacteria in the culture at different periods may be : (1) Total count. It includes both living and dead bacteria, or (2) Viable count. It includes only the living bacteria. Microbial concentration can be measured in terms of cell concentration, i.e. the number of viable cells per unit volume of culture, or of biomass concentration, i.e. dry weight of cells per unit volume of culture.

Bacterial count is of Growth Phases

1. Lag Phase. In this phase there is increase in cell size but not multiplication. Time is required for adaptation (synthesis of new enzymes) to new environment. During this phase vigorous metabolic activity occurs but cells do not divide. Enzymes and intermediates are formed and accumulate until they are present in concentration that permits growth to start. Antibiotics have little effect at this stage.

2. Exponential Phase or Logarithmic (Log) Phase. The cells multiply at the maximum rate in this exponential phase, i.e. there is linear relationship between time and logarithm of the number of cells. Mass increases in an exponential manner. This continues until one of two things happens: either one or more nutrients in the medium become exhausted, or toxic metabolic products, accumulate and inhibit growth. Nutrient oxygen becomes limited for aerobic organisms. In exponential phase, the biomass increases exponentially with respect to time, i.e. the biomass doubles with each doubling time. The average time required for the population, or the biomass, to double is known as the generation time or doubling time. Linear plots of exponential growth can be produced by plotting the logarithm of biomass concentration as a function of time. Importance : Antibiotics act better at this phase.

3.  Maximal Stationary Phase. Due to exhaustion of nutrients or accumulation of toxic products death of bacteria starts and the growth cease completely. The count remains stationary due to balance between multiplication and death rate. Importance: Production of exotoxins, antibiotics, metachromatic granules, and spore formation takes place in this phase.

4. Decline phase or death phase. In this phase there is progressive death of cells. However, some living bacteria use the breakdown products of dead bacteria as nutrient and remain as persister.

Recently, some authors are dividing the growth curve into six phases by the letters A to F as follows
(a) Lag phase- Growth rate is zero.
(b) Acceleration phase- Increasing growth rate. C Exponential phase — Constant growth rate.
(c) Retardation phase- Growth rate is decreasing.
(e) Maximum stationary phase- Growth rate is zero. F Decline phase- Growth rate is negative (death).

use in the examination of water and milk

Genetic.

Genetic is the science that deals with heredity. Thus, it is the study of the mechanisms by which different characteristics are passed on from parents to offsprings (progeny).

Gene. Genes are genetic determinants and thus control heredity and determine properties of the organism. The genes are functional units of the chromosomes. Synthesis of protein components and enzymes of a cell is regulated by genes. DNA is responsible for both gene function and replication. By replication heredity or stability of a type is maintained. An organism containing a normal gene is known as 'wild type'. Genes may rarely mutate (change) resulting in heritable variations called mutations (See chapter 8). The changed organism is called a mutant.

Genotype. It is the genetic determinant of a cell.

Phenotype. This is the structural and physiological manifestations of the organism due to a particular genotype.

Genome. Genome is the entire set of genes and thus is the totality of genetic information in an organism.

BACTERIAL GENOME (PROKARYOTIC GENOME) 

Genes are carried on :
1. Bacterial chromosome. Chromosomes carry most prokaryotic genes. Genes essential for bacterial growth are carried on chromosome. It is present in all bacteria. Only one chromo-some is present in a bacterial nucleoid. Bacterial chromosome is a single circle containing about 4000 kbp (kilobase pairs) of DNA. DNA is a double stranded helical structure. A molecule of DNA consists of many mononucleotides. A mononucleotide consists of a molecule of sugar, a molecule of phosphate and a molecule of base. In each strand of DNA, molecules of phosphate and sugar alternate, and one of the four bases present in DNA is attached with the sugar. The four bases are adenine, thymine, guanine and cytosine. A base of a strand joins with its complementary base of the other strand. Adenine is always complementary to thymine, and guanine to cytosine. During cell division, duplication of chromosome occurs so that each daughter cell receives an identical set.

2.Plasmid. Certain bacteria contain plasmids. Plasmids carry genes associated with specialized function. These are extra-chromosomal genetic elements. Plasmid is a circular double stranded DNA having several to 100 kbp. Plasmids replicate autonomously and they code for functions which are normally not indispensable. In some cases, plasmids may be transferred from one cell to another and thus may carry sets of specialized genetic information through a population, e.g. Drug resistance plasmids (R factors) may render diverse bacteria resistant to antimicrobial drugs.

3.Transposon. Transposons are genetic elements with DNA sequences of several kbp. They can migrate from one genetic

locus to another. Transfer of transposons can occur between one plasmid to another, or between plasmid and chromosome within a bacterial cell. The process is called transposition. Transposons carry genes for specialized functions, e.g. antibiotic resistance. Transposons do not contain genetic information for their replication.

NOTE: Bacteria infected with bacterial viruses (bacteriopha­ges) contain the genes of the phage. Lysogenic bacteria are the bacteria which contain nonlytic prophage state of temperate phages.

Phenotypic changes that can occur in bacteria due to Mutation:

1.   Loss of capsule formation by capsulated bacteria.
2.   Change in colony characters.
3.   Change in fermentation activity.
4.   Loss of sensitivity to antibiotics.
5.   Loss of sensitivity to bacteriophage (Bacterial virus).

TRANSFER OF GENE
Transfer of DNA is widespread among bacterial cells. In intercellular transfer, the genetic material passes from the donor cell to the recipient cell. It leads to genetic diversity of bacteria. Intercellular transfer of DNA between bacterial strains can occur by conjugation, transduction and transformation.

1.   Conjugation
In conjugation, a suitable donor cell (male) comes near a recipient cell (female), establishes direct cell-to-cell contact and transfers genetic material. Plasmids are most frequently transferred by conjugation. Plasmids can also mobilize portions of chromosome for transfer. This is mediated by a fertility or F factor which is carried on a plasmid. Sex pilus is responsible for the attachment of donor (F*) cell and recipient cell (F) in bacterial conjugation (mating) process. Cell with sex pilus is the male and without sex pilus is the female bacteria.

Example: Transfer of antibiotic resistance can occur by conjugation. Transfer of drug resistant plasmid is called R-factor (Resistance plasmid). This occurs via sex pilus from the male (donor) cell to the female (recipient) cell.

2.Transduction
Transduction is phage-mediated. In transduction, genetic material of donor bacterial cell is enclosed in a bacterial virus (phage) and transferred to the recipient cell.

3.Transformation
In transformation, the recipient cell directly takes up naked DNA released from the donor cell altering its genotype. It can occur in the medium. Natural transformation also can occur.

Sterilization

Sterilization is the killing or removal of all microorganisms, including bacterial spores which are highly resistant. Sterilization is an absolute term, i.e. the article must be sterile meaning the absence of all microorganisms.

Disinfection is the killing of many, but not all microorganisms. It is a process of reduction of number of contaminating organisms to a level that cannot cause infection, i.e. pathogens must be killed. Some organisms and bacterial spores may survive.

Disinfectants are chemicals that are used for disinfection. Disinfectants should be used only on inanimate objects.

Antiseptics are mild forms of disinfectants that are used externally on living tissues to kill microorganisms, e.g. on the surface of skin and mucous membranes.


Uses of Sterilization
1.   Sterilization for Surgical Procedures: Gloves, aprons, surgical instruments, syringes etc. are to be sterilized.

2.   Sterilization in Microbiological works like preparation of culture media, reagents and equipments where a sterile condition is to be maintained.


CLASSIFICATION OF METHODS 
Sterilization and disinfection are done by :
(A). Physical Agents
     1.   Heat
     2.   Radiation
     3.   Filtration

(B). Chemical Agents
In practice, certain methods are placed under sterilization which in fact do not fulfill the definition of sterilization such as boiling for 1/2 hr and pasteurization which will not kill spores.

STERILIZATION BY HEAT
Heat is most effective and a rapid method of sterilization and disinfection. Excessive heat acts by coagulation of cell proteins. Less heat interferes metabolic reactions. Sterilization occurs by heating above 100°C which ensure lolling of bacterial spores. Sterilization by hot air in hot air oven and sterilization by autoclaving are the two most common method used in the laboratory.

Types of Heat :
 A.  Sterilization by moist heat
 B.  Sterilization by dry heat

A. Sterilization by Moist Heat
Moist heat acts by denaturation and coagulation of protein, breakage of DNA strands, and loss of functional integrity of cell membrane.

(I). Sterilization at 100°C
1.   Boiling. Boiling at 100°C for 30 minutes is done in a water bath. Syringes, rubber goods and surgical instruments may be sterilized by this method. All bacteria and certain spores are killed. It leads to disinfection.

2.   Steaming. Steam (100°C) is more effective than dry heat at the same temperature as: (a) Bacteria are more susceptible to moist heat, (b) Steam has more penetrating power, and (c) Steam has more sterilizing power as more heat is given up during condensation.

Steam Sterilizer. It works at 100°C under normal atmospheric pressure i.e. without extra pressure. It is ideally suitable for sterilizing media which may be damaged at a temperature higher than 100°C.

It is a metallic vessel having 2 perforated diaphragms (Shelves), one above boiling water, and the other about 4" above the floor. Water is boiled by electricity, gas or stove. Steam passes up. There is a small opening on the roof of the instrument for the escape of steam. Sterilization is done by two methods :

(a) Single Exposure for 11/2 hours. It leads to disinfection.

(b) Tyndallization (Fractional Sterilization). Heat labile media like those containing sugar, milk, gelatin can be sterilized by this method. Steaming at 100°C is done in steam sterilizer for 20 minutes followed by incubation at 37°C overnight. This procedure is repeated for another 2 successive days. That is 'steaming' is done for 3 successive days. Spores, if any, germinate to vegetative bacteria during incubation and are destroyed during steaming on second and third day. It leads to sterilization.

II. Sterilization above 100°C: Autoclaving
Autoclaving is one of the most common methods of sterilization. Principle: In this method sterilization is done by steam under pressure. Steaming at temperature higher than 100°C is used in autoclaving. The temperature of boiling depends on the surrounding atmospheric pressure. A higher temperature of steaming is obtained by employing a higher pressure. When the autoclave is closed and made air-tight, and water starts boiling, the inside pressures increases and now the water boils above 100°C. At 15 ib per sq. inch pressure, 121°C temperatures is obtained. This is kept for 15 minutes for sterilization to kill spores. It works like a pressure cooker.

'Sterilization holding time' is the time for which the entire load in the autoclave requires to be exposed.

Autoclave is a metallic cylindrical vessel. On the lid, there are : (1) A gauge for indicating the pressure, (2) A safety valve, which can be set to blow off at any desired pressure, and (3) A stopcock to release the pressure. It is provided with a perforated diaphragm. Water is placed below the diaphragm and heated from below by electricity, gas or stove. Working of Autoclave. (a) Place materials inside, (b) Close the lid. Leave stopcock open, (c) Set the safety valve at the desired pressure, (d) Heat the autoclave. Air is forced out and eventually steam ensures out through the tap, (e) close the tap. The inside pressure now rises until it reaches the set level (i.e. 15 Win), when the safety valve opens and the excess steam escapes, (f) Keep it for 15 minutes (holding time), (g) Stop heating, (h) Cool the autoclave below 100°C, (i) Open the stopcock slowly to allow air to enter the autoclave.

Checking of Autoclave for Efficiency. Methods :
(i)  Spores of Bacillus stearothermophilus are used. Spores withstand 121°C heat for up to 12 min. Strips containing this bacteria are included with the material being autoclaved. Strips are cultured between 50°C and 60°C for surviving spores. If the spores are killed the autoclave is functioning properly.
(ii)Automatic Monitoring System.


III. Sterilization below 100°C
1. Pasteurization. Pasteurization is heating of milk to such temperature and for such a period of time so as to kill pathogenic bacteria that may be present in milk without changing colour, flavour and nutritive value of the milk. Mycobacterium bovis, Salmonella species, Escherichia coli and Brucella species may be present in milk. It does not sterilize the milk as many living organisms including spores are not destroyed..

Methods of Pasteurization
(i)  Flash Method. It is "high temperature- short time method". Heating is done at 72°C for 15 seconds.
(ii) Holding Method. Heating is done between 63°C and 66°C for 30 minutes.

2. Inspissation. Inspissation is done between 75°C to 80°C. Inspissation means stiffening of protein without coagulation as the temperature is below coagulation temperature. Media containing serum or egg is sterilized by heating for 3 successive days. It is done in 'Serum Inspissator'.


B. Sterilization by Dry Heat
Mechanisms. (1) Protein denaturation, (2) Oxidative damage, (3) Toxic effect of elevated electrolyte (in absence of water).

Dry heat at 160°C (holding temperature for one hour is required to kill the most resistant spores). The articles remain dry. It is unsuitable for clothing which may be spoiled.

1.   Red Heat. Wire loops used in microbiology laboratory are sterilized by heating to 'red' in bunsen burner or spirit lamp flame. Temperature is above 100°C. It leads to sterilization.

2.   Flaming. The article is passed through flame without allowing it to become red hot, e.g. scalpel. Temperature is not high to cause sterilization.

3.   Sterilization by Hot Air

Hot Air Oven (Sterilizer). It Is one of the most common method used for sterilization. Glass wares, swab sticks, all-glass syringes, powder and oily substances are sterilized in hot air oven. For sterilization, a temperature of 160°C is maintained (holding) for one hour. Spores are killed at this temperature. It leads to sterilization.

Hot Air Oven is an apparatus with double metallic walls and a door. There is an air space between these walls. The apparatus is heated by electricity or gas at the bottom. On heating, the air at the bottom becomes hot and passes between the two walls from below upwards, and then passes in the inner chamber through the holes on Me top of the apparatus. A thermostat is fitted to maintain a constant temperature of 160°C.

TYPES OF CULTURE MEDIA

Media are of different types on consistency and chemical composition.

A. On Consistency:
1.   Solid Media. Advantages of solid media: (a) Bacteria may be identified by studying the colony character, (b) Mixed bacteria can be separated. Solid media is used for the isolation of bacteria as pure culture. 'Agar' is most commonly used to prepare solid media. Agar is polysaccharide extract obtained from seaweed. Agar is an ideal solidifying agent as it is : (a) Bacteriologically inert, i.e. no influence on bacterial growth, (b) It remains solid at 37°C, and (c) It is transparent.
2.     Liquid Media. It is used for profuse growth, e.g. blood culture in liquid media. Mixed organisms cannot be separated.

B. On Chemical Composition :
1.   Routine Laboratory Media
2.     Synthetic Media. These are chemically defined media prepared from pure chemical substances. It is used in research work.

ROUTINE LABORATORY MEDIA
These are classified into six types: (1) Basal media, (2) Enriched media, (3) Selective media, (4) Indicator media, (5) Transport media, and (6) Storage media.

1.   BASAL MEDIA. Basal media are those that may be used for growth (culture) of bacteria that do not need enrichment of the media. Examples: Nutrient broth, nutrient agar and peptone water. Staphylococcus and Enterobacteriaceae grow in these media.

2.     ENRICHED MEDIA. The media are enriched usually by adding blood, serum or egg. Examples: Enriched media are blood agar and Lowenstein-Jensen media. Streptococci grow in blood agar media.

3.   SELECTIVE MEDIA. These media favour the growth of a particular bacterium by inhibiting the growth of undesired bacteria and allowing growth of desirable bacteria. Examples: MacConkey agar, Lowenstein-Jensen media, tellurite media (Tellurite inhibits the growth of most of the throat organisms except diphtheria bacilli). Antibiotic may be added to a medium for inhibition.

4.     INDICATOR (DIFFERENTIAL) MEDIA. An indicator is included in the medium. A particular organism causes change in the indicator, e.g. blood, neutral red, tellurite. Examples: Blood agar and MacConkey agar are indicator media.

5.   TRANSPORT MEDIA. These media are used when specie-men cannot be cultured soon after collection. Examples: Cary-Blair medium, Amies medium, Stuart medium.

6.   STORAGE MEDIA. Media used for storing the bacteria for a long period of time. Examples: Egg saline medium, chalk cooked meat broth.

COMMON MEDIA IN ROUTINE USE

Nutrient Broth. 500 g meat, e.g. ox heart is minced and mixed with 1 litre water. 10 g peptone and 5 g sodium chloride are added, pH is adjusted to 7.3. Uses: (1) As a basal media for the preparation of other media, (2) To study soluble products of bacteria.

Nutrient Agar. It is solid at 37°C. 2.5% agar is added in nutrient broth. It is heated at 100°C to melt the agar and then cooled.

Peptone Water. Peptone 1% and sodium chloride 0.5%. It is used as base for sugar media and to test indole formation.

Blood Agar. Most commonly used medium. 5-10% defibrinated sheep or horse blood is added to melted agar at 45-50°C. Blood acts as an enrichment material and also as an indicator. Certain bacteria when grown in blood agar produce haemolysis around their colonies. Certain bacteria produce no haemolysis. Types of changes : (a) beta (p) haemolysis. The colony is surrounded by a clear zone of complete haemolysis, e.g. Streptococcus pyogenes is a beta haemolytic streptococci, (b) Alpha (a) haemolysis. The colony is surrounded by a zone of greenish discolouration due to formation of biliverdin, e.g. Viridans streptococci, (c) Gamma (y) haemolysis, or, No haemolysis. There is no change in the medium surrounding the colony,

Chocolate Agar or Heated Blood agar. Prepared by heating blood agar. It is used for culture of pneumococcus, gonococcus, meningococcus and Haemophilus. Heating the blood inactivates inhibitor of growths.

MacConkey Agar. Most commonly used for enterobac­teriaceae. It contains agar, peptone, sodium chloride, bile salt, lactose and neutral red. It is a selective and indicator medium :

(1)   Selective as bile salt does not inhibit the growth of enterobactericeae but inhibits growth of many other bacteria.

(2)   Indicator medium as the colonies of bacteria that ferment lactose take a pink colour due to production of acid. Acid turns the indicator neutral red to pink. These bacteria are called 'lactose fermenter', e.g. Escherichia coll. Colourless colony indicates that lactose is not fermented, i.e. the bacterium is non-lactose fermenter, e.g. Salmonella. Shigella, Vibrio.

Mueller Hinton Agar. Disc diffusion sensitivity tests for antimicrobial drugs should be carried out on this media as per WHO recommendation to promote reproducibility and comparability of results.

Hiss's Serum Water Medium. This medium is used to study the fermentation reactions of bacteria which can not grow in peptone water sugar media, e.g. pneumococcus, Neisseria, Corynebacterium.

Lowenstein-Jensen Medium. It is used to culture tubercle bacilli. It contains egg, malachite green and glycerol. (1) Egg is an enrichment material which stimulates the growth of tubercle bacilli, (2) Malachite green inhibits growth of organisms other than mycobacteria, (3) Glycerol promotes the growth of Mycobacterium tuberculosis but not Mycobacterium bovis.

Dubos Medium. This liquid medium is used for tubercle bacilli. In this medium drug sensitivity of tubercle bacilli can be carried out. It contains 'tween 80', bovine serum albumin, casein hydrolysate, asparagin and salts. Tween 80 causes dispersed growth and bovine albumin causes rapid growth.

Loeffler Serum. Serum is used for enrichment. Diphtheria bacilli grow in this medium in 6 hours when the secondary bacteria do not grow. It is used for rapid diagnosis of diphtheria and to demonstrate volutin granules. It contains sheep, ox or horse serum.

Tellurite Blood Agar. It is used as a selective medium for isolation of Cotynebacterium diphtheriae. Tellurite inhibits the growth of most secondary bacteria without an inhibitory effect on diphtheria bacilli. It is also an indicator medium as the diphtheria bacilli produce black colonies. Tellurite metabolized to tellbrism, which has black colour.

EMB (Eosin-methylene blue) Agar. A selective and differential medium for enteric Gram-negative rods. Lactose-fermenting colonies are coloured and nonlactose-fermenting colonies are nonpigmented. Selects against gram positive bacteria.

XLD (Xylose Lysine Deoxychoiate). It is used to isolate Salmonella and Shigella species from stool specimens. This is a selective media.

SS (Salmonella-Shigella) Agar. It is a selective medium used to isolate Salmonella and Shigella species. SS Agar with additional bile salt is used if Yersinia enterocolitica is suspected.

DCA (Desoxycholate Citrate Agar). It is used for isolation of Salmonella and Shigella. The other enteric bacteria are mostly inhibited (a selective medium). It is also a differential (indicator) medium due to presence of lactose and neutral red.

Tetrathionate Broth. This medium is used for isolating Salmonella from stool. It acts as a selective medium. It inhibits normal intestinal bacteria and permits multiplication of Salmonella.

Selenite F Broth. Uses and functions are same as that of tetrathionate broth.

Thiosulphate-Citrate-Bile-Sucrose (TCBS) Agar. TCBS agar is a selective medium used to isolate Vibrio cholerae and other Vibrio species from stool.

Charcoal-yeast agar. Used for Legionella pneumophila. Increased concentration of iron and cysteine allows growth.

Tellurite-Gelatin Agar Medium (TGAM). It may be used as transport, selective and indicator medium.

Alkaline peptone water. See under Vibrio. (Chapter 51).

Campylobacter Medium. This selective medium is used to isolate Campylobacter jejuni and Campylobacter coli from stool.

Cary-Blair Medium. It is used as a transport medium for faeces that may contain Salmonella, Shigella, Vibrio or Cam­pylobacter species.

Amies medium is used for gonococci and other pathogens.

Peptone Water Sugar Media. These indicator media are used to study 'Sugar fermentation'. 1 % solution of a sugar (lactose, glucose, mannitol etc) is added to peptone water containing Andrade's indicator in a test tube. A small inverted Durham tube is placed in the medium. The media are colourless. After culture, change of a medium to red colour indicates acid production. Gas, if produced collects in Durham tube.

Motility Indole Urea (MIU) Medium. This is used to differentiate enterobacteria species by their motility, urease, and indole reactions.

TSI (Triple sugar iron) Agar- See chapter 53.

KIA (Kligler Iron Agar). This is a differential slope medium used in the identification of enteric bacteria. The reactions are based on the fermentation of lactose and glucose and the production of hydrogen sulphide (chapter 53).

Christensen's Urea Medium. This is used to identify urea splitting organisms, e.g. Proteus. A purple pink colour indicates urea splitting (See chapter 53).

Bordet-Gengou Medium. This medium is used for culture of Bordetella pertussis. Increased concentration of blood allows growth. It contains agar, potato, sodium chloride, glycerol, peptone and 50% horse blood. Penicillin may be added to it.

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Host-parasite Interactions

Infectious Diseases. These are caused by infectious agents which are bacteria, viruses, fungi, protozoa and helminths.

Parasite is a living organism (bacteria, viruses, fungi, protozoa, helminths) that lives in another organism, and receives shelter and nourishment. However, in medical science parasitology traditionally deals with animal parasites- protozoa and helminths.

Strict or obligate parasite is an organism that cannot live without a host. That is they have no free-living existence. Examples: Treponema pallidum, viruses, malarial parasite.

Facultative parasite is an organism that has both a free-living and a parasitic existence, e.g. Clostridium species, Pseudomonas species.

Pathogen. Pathogen is an organism which can cause disease.

Nonpathogen. An organism that does not cause disease. It may be a member of normal flora.

Opportunistic pathogen is an organism (nonpathogen, commensal or saprophyte) that can cause disease only in immunocompromised individuals that is having impaired
resistance. Example : Cytomegalovirus, Pneumocystis carinii, Atypical mycobacteria, opportunist fungi.

Saprophyte is an organism that lives on dead organic matter.

NORMAL FLORA (Commensals)
Microorganisms that is present on the skin and mucous membrane of normal (healthy) persons. One particular microorganism of the normal flora may be a nonpathogen, or opportunistic pathogen. Normal flora is of two types: (1) Resident flora. These are microorganisms regularly present in the region at a given age, e.g. Viridans streptococci in mouth and throat, Escherichia coli in intestine, (2) Transient flora. The microorganism is present only for hours to weeks, e.g. Streptococcus pyogenes in throat. Microorganisms of transient flora play no role when the normal resident flora remains intact. But if the resident flora is disturbed than the microorganisms of transient flora may colonize and produce disease. See chapter 62.

Beneficial Functions of Normal Flora. Examples: (1) In mouth and lower b jvel an invading pathogen may fail to compete for nutrients and receptor sites with normal flora, (2) Some bacteria of the bowel produce antimicrobial substances, (3) In new born, bacteria acts as a powerful stimulus for the development of immune system, (4) Bacteria of the gut can produce 
vitamin K.

Harmful Effects of Normal Flora. Clinical diseases by opportunist pathogen of normal flora arise under : (1) when the organism leaves the normal site and localizes to another site, e.g. Escherichia coli in the urinary tract from gut, (2) competitive advantage due to antibiotic therapy, e.g. colitis by Clostridium difficile, (3) In immunocompromised individuals.

HOST

Host is the harbouring organism of a parasite. They fall into three groups or classes:

1.   Definitive host. In this host the adult stage of animal parasites lives and sexual reproduction takes place. Man is the definitive host for all animal parasites except malarial parasites and hydatid tapeworm.

2.  Intermediate host. In this host the asexual reproduction takes place, or the larval stages of animal parasites develops. When development of larval stage takes place in two different hosts they are called 'first' and 'second' intermediate hosts. Man is the intermediate host for malarial parasites and hydatid tapeworm. Man is both definitive and intermediate host for Taenia solium and Trichinella spiralis.

3.   Paratenic host. A carrier or transport host.

Note : The term infestation is used when the parasite lives on the outer surface. They are arthropodes- mites, ticks and insects.

INFECTION
Infection is the multiplication of an infectious agent within the body. Multiplication of pathogenic bacteria (e.g. Salmonella typhi) even if the person is asymptomatic is taken as an infection. Multiplication of bacteria of normal flora at its normal site is not an infection. However, if they multiply and cause disease it is an infection, e.g. Escherichia coli when causes diarrhoea.

An infection involves the following : (1) Source or reservoir of infectious agent, (2) Transmission of the infectious agent from the source to the host (3) Susceptible host- Portal or route of entry of the agent in the host, its localization, multiplication and finally host-parasite interactions which result in either (a) Destruction of the agent or, (b) Infectious disease.

Source (Reservoir) :
1. Human Source.
(a) Exogenous source : Patient or carrier,

(b) Endogenous source : The individual himself.

Carrier. A person with asymptomatic infection which can be transmitted to another susceptible person. An individual may be a carrier : (a) in the incubation period (Incubatory carrier), e.g. in measles, (b) during convalescence (convalescent carrier), e.g. typhoid fever, or (c) for a prolonged period, e.g. typhoid fever.

2. Foods and Drinks
(a) Food :Any contaminated food, (b) Water contaminated with bacteria of typhoid fever, cholera, diarrhoea and dysentery,
(c) Milk contaminated with salmonella, M. bovis.

3. Animals : Zoonoses are diseases which are transmitted from infected animals to humans.
(a) Cow : Bovine tuberculosis, brucellosis by Brucella abortus, Salmonella food poisoning, anthrax, Taenia saginata, (b) Fowl. Salmonella food poisoning by eggs and meat, (c) Dog. Rabies, hydatid disease, Weil's disease, (d) Horse. Tetanus and glanders, (e) Goat. Anthrax and brucellosis (by B. melitensis ), (f) Sheep. Anthrax and tetanus, (g) Cat. Cat scratch disease, (h) Rat. Plaque, Weil's disease, (i) Parrot and pigeons. Psittacosis.

4. Soil. Tetanus, gas gangrene.

Modes of Transmission

1.   Water-borne, e.g. cholera and other diarrhoea) diseases, enteric fever from contaminated water.

2.   Food-borne (contaminated food) e.g. enteric fever, salmo­nella food poisoning (e.g. eggs of duck, foul). Milk and milk products- enteric fever, bovine tuberculosis.

3.     Air-borne e.g. Droplets. During coughing, sneezing and talking: Diphtheria, tuberculosis, measles, chickenpox, mumps, influenza,

4.   Dust-borne. e.g. tuberculosis,

5.   Soil- Tetanus, gas gangrene.

6.     Contaminated fomites like beddings, clothings, utensils: Diphtheria, enteric fever, food poisoning.

7.   Direct contact- STD like gonorrhoea, syphilis, AIDS.

8.   Transplacental: Rubella, toxoplasma, congenital syphilis.

9.   Insect borne. (a) Actively, e.g. malaria, filaria, kala azar, dengue, plague, yellow fever, (b) Passively, e.g. diarrhoea) diseases, enteric fever, salmonella food poisoning.


Portal or Route of Entry
(1) Alimentary system by ingestion, (2) Respiratory system by inhalation, (3) Genitourinary system, (4) Skin due to trauma, bite of insects, (5) Placenta.

Self-infection and cross-infection
Self-infection is the infection that occurs from the patient's own flora. Examples : (i) infection of an wound of a patient by staphylococci carried by the individual in his nose, (2) coliforms and anaerobes released from his bowel during surgery.

Cross infection is the infection derived from other patients or healthy carriers by direct spread as droplets during talking, coughing, sneezing, by air-born dust, food, fluids etc. Cross-infection is common in hospitals.

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BACTERIAL TOXINS

Bacterial toxins are exotoxins and endotoxins. Characteristics and differences of exotoxins and endotoxin are listed in down the page.

EXOTOXINS
Exotoxin producing bacteria

1.   Corynebacterium diphtheriae. Strains that carry a temperate bacteriophage are toxigenic causes diphtheria. Exotoxin inhibits protein synthesis and causes cell death. Causes diphtheria.

2.   Clostridium tetani. Exotoxin blocks action of inhibitory neurones of spinal cord. Causes tetanus.

3.   Clostridium perfringens. (a) Causes gas gangrene. Exotoxin (alpha toxin) has lacithinase activity and thereby causes cell death, (b) Enterotoxin causes hyper secretion of water and electrolytes in diarrhoea.

4.     Clostridium botulinum. Exotoxin causes paralysis of deglutination and respiratory muscles. It blocks release of acetylcholine of synapses and neuromuscular junctions. Causes botulism.

5.   Vibrio cholerae 01 and 0139. Enterotoxin (Exotoxin) causes hyper secretion of water and electrolytes within gut in diarrhoea.

6.   Enterotoxigenic E. coll. Produce enterotoxin (LT- heat labile exotoxin) causes hypersecretion of water and electrolytes within gut.

7.   Shigella dysenteriae type 1 (Shiga bacillus). Exotoxin causes acute inflammation.

8.   Staphylococcus aureus- some strains : (a) Toxic shock syndrome toxin-1. Causes toxic shock syndrome. (b) Staphylococcal enterotoxin causes toxin type food poisoning and stimulates vomiting centre of brain.

9.   Streptococcus pyogenes. Pyrogenic (Erythrogenic) exotoxin causes scarlet fever and toxic shock syndrome.

NOTE : Enterotoxins are exotoxins that are associated with diarrhoea) diseases and food poisoning. Bacteria producing enterotoxins are V. cholerae, enterotoxigenic E. coli (ETEC), some strains of S. aureus, V. parahaemolyticus, Y. enterocolitica, Aeromonas species, and C. perfringens.

Toxoid. Toxoid is modified exotoxin. An exotoxin has two main properties : 
(1) toxicity, and
(2) antigenicity. In toxoid, the toxicity of the toxin is destroyed but its antigenicity is preserved. As such toxoids e.g. diphtheria toxoid, tetanus toxoid can be safely used for vaccines. Toxins can be converted to toxoid by different methods e.g. formalin treatment.

ENDOTOXINS

Endotoxins are the integral part of the cell walls of Gram-negative bacteria, and are liberated when bacteria are disintegrated (lysed). Cell wall of Gram negative bacteria contain lipopolysaccharides (LPS, endotoxin) which consists of : (1) Lipid A. This is the endotoxin and is the core, and (2) Polysaccharide form coat. This is the 0 antigen which can induce specific immunity. Physiological, pathological and clinical effects of endotoxins of different Gram negative bacteria are similar. These are :

1. Fever. The endotoxin acts on mononuclear phagocytes (monocytes/macrophages), with liberation of interleukin-1 (endogenous pyrogen). Interleukin-1 acts on thermoregulatory centre. Chill is due to widespread arteriolar and venular constriction.
2. Leucopenia occurs early with onset of fever. It may be followed by leucocytosis.

3. Hypoglycaemia. LPS enhances glycolysis in many cell types and can lead to hypoglycaemia.

4.  Hypotension occurs early in Gram-negative bacteraemia.

5.  Shock. 'Endotoxic' or 'septic' shock may develop in severe Gram-negative bacteraemia (See chapter 4).

6.      Activation of complement. Endotoxin activates complement system by alternative pathway.

7.  Disseminated Intravascular Coagulation (DIC). DIC may occur in Gram negative bacteraemia. It is initiated on activation of factor XII (Hageman factor) of coagulation cascade by endotoxin which finally leads to conversion of fibrinogen to fibrin. Endotoxin leads platelets to adhere on vascular endothelium. Endotoxin can activate plasminogen to plasmin which acts on fibrin producing fibrin-split products. Shwartzman phenomenon is taken as a specialized form of DIC.

8.  Death may occur due to shock and/or DIC.

NOTE: Peptidoglycan of Gram-positive Bacteria: Peptidoglycan of Gram-positive bacteria released during infection may produce similar activities as LPS of Gram-negative bacteria. However, peptidoglycan is much less potent than LPS.

Characteristics and Differences of Exotoxins and Endotoxins

Endotoxin:
1.   Integral part of the cell wall of Gram-negative bacteria. Released on bacterial death and in part during growth. Release is not required for biologic activity.
2.   Formed only by Gram-negative bacteria
3.   Lipopolysaccharides. Lipid A portion is responsible for toxicity.
4.   No specific receptor.
5.   Moderately toxic. Fatal to animals in large doses.
6.   Relatively heat stable. Toxicity is not destroyed above 60°C for hours.
7.   Weakly antigenic. Antibodies are protective.
8.   Not converted to toxoid.
9.   Synthesis directed by chromosomal genes.
10.  Usually produce fever in the host by release of interleukin-1 and other mediators..]

Exotoxins:
1.Excreted by living cells
2.   Produced by Gram-positive and Gram-negative bacteria
3.   Polypeptides
4.   Usually bind to specific receptors on cells
5.   Highly toxic. Fatal to animals in very small doses
6.   Relatively heat labile. Toxicity destroyed over 60°C
7.   Highly antigenic. Stimulate formation of antitoxin. Antitoxin neutralizes the toxin
8.   Converted to toxoid by formalin. Toxoid is nontoxic but antigenic. Toxoids are used to immunize, e.g. tetanus toxoid
9.   Usually controlled by extra-chromosomal genes, e.g. plasmids, phage gene
10.  Usually do not produce fever in the host.

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MECHANISMS OF ACTION OF ANTIMICROBIAL DRUGS

Selective Toxicity. Selective toxicity is the property of an ideal antimicrobial agent. Selective toxicity means that the drug is harmful to a parasite but not to the host. Usually the effect is relative rather absolute, i.e. a drug in a concentration tolerated by the host may damage an infecting microorganism. Selective toxicity may be a function of a specific receptor required for drug attachment, or it may depend on inhibition of biochemical events essential to the organism but not to the host. The mechanisms are discussed under four headings: (1) Inhibition of cell wall synthesis, (2) Inhibition of cell membrane function, (3) Inhibition of protein synthesis, and (4) Inhibition of nucleic acid synthesis.

Classification on mode of Action:
1. Inhibition of cell wall synthesis. Penicillins, cephalo­sporin, vancomycin, bacitracin, cycloserin are examples.

All (3-Iactarn drugs like penicillins, cephalosporins are selective inhibitors of bacterial cell wall synthesis and therefore active against growing bacteria. Mechanism of action: Initial step is the binding of the drug to specific drug receptor PBPs (Penicillin- binding proteins) on bacteria. There are 3 to 6 PBPs having different effects. At least some of which are enzymes involved in transpeptidation (cross-linking) reactions. After attachment, peptidoglycan synthesis is inhibited as final transpeptidation is blocked. Then there occurs inactivation of an inhibitor of autolytic enzyme in the cell wall. This activates the autolytic enzymes in the cell wall that results in lysis resulting in bacterial death. Organisms with defective autolysin function are inhibited but not killed by l3dactam drugs, and they are said to be "tolerant".

The Gram-positive and Gram-negative bacteria differ in susceptibility to penicillins or cephalosporins on structural differences in their cell walls that decide binding, penetration, and activity of the drugs. The differences in cell wall are in the amount of peptidoglycan, presence of receptors and lipids, nature of cross-linking and activity of autolytic enzymes. Peptidoglycan layer of the cell wall is much thicker in Gram-positive than in Gram-negative bacteria.

Lack of toxicity of p-lactam drugs to animal cells is attributed to the absence of bacterial type cell wall with its peptidoglycan in animal cells.

Extended-spectrum P lactum (ESBLs) are enzymes that mediate resistance to extended-spectrum (third generation) cephalosporins (e.g., ceftazidime, cefotaxime, and ceftriaxone) and monobactams (e.g., aztreonam) but do not affect cephamycins (e.g., cefoxitin and cefotetan) or carbapenems (e.g., meropenem or imipenem). Production of ESBLs can be screened by broth microdilution and disk diffusion screening tests using selected antimicrobial agents.

2. Alteration of cell membrane function. Polymyxin, amph­otericin B, imidazole are examples.
These drugs act by disruption of the functional integrity of the cytoplasmic membrane. Macromolecules and ions escape from the cell causing cell damage or death. Selective chemotherapy is possible as the cytoplasmic membrane of bacteria and fungi has a structure different from that of animal cells, and can be more readily disrupted by certain chernothe rape utics.

3. Inhibition of protein synthesis. These drugs inhibit protein synthesis in bacteria. Bacteria have 70S ribosomes, whereas mammalian cells have 80S ribosomes. Subunits of each type of ribosome, their chemical composition, and functional specifities differ. Thus a drug can inhibit protein synthesis in bacterial ribosomes but not in mammalian ribosomes.

(a)   Action on 50S ribosomal subunit. Chloramphenicol, erythromycin and chindamycin are examples.
(b) Action on 30S ribosomal subunit. Tetracycline and aminoglycosides are examples.

4. Inhibition of nucleic acid synthesis. These drugs inhibit nucleic acid synthesis by different mechanisms. (a) Inhibition of nucleotide synthesis. Sulphonamides, trimethoprin Sulphonamides compete for the enzyme required for essential metabolite PABA involved in the synthesis of folic acid needed for synthesis of nucleic acid. (b) Inhibition of DNA synthesis. Quinolones block DNA gyrase. (c) Inhibition of mRNA synthesis- Rifampin.

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RESISTANCE TO ANTIMICROBIAL DRUGS

A. Mechanisms of Drug Resistance. Microoganisms exhibit resistance to antimicrobial drugs by different mechanisms.

1.   Microorganisms produce enzymes that destroy the active drug. Examples: P-lactamases (Penicillinases) produced by certain bacteria destroy penicillin. Staphylococci resistant to penicillin G produce a P-lactamase that destroys the drug. Other P-lactamases are produced by Gram-negative rods.

2.   Microorganisms change their permeability to the drug, e.g. tetracycline accumulate in susceptible bacteria but not in resistant bacteria.

3.   Microorganisms develop an altered metabolic pathway that bypasses the reaction inhibited by the drug. Sulphonamide resistant bacteria do not require extracellular PABA, but can utilize preformed folic acid.

4.   Microorganisms develop an altered structural target for the drug: Erythromycin resistant organisms have on altered receptor on the 50S subunit of the ribosome. Aminoglycosides­resistant is due to alteration or loss of a specific protein in the 30S subunit of the bacterial ribosome that serve as a binding site in susceptible organisms. Resistance to some penicillins and cephalosporins occurs due to alteration or loss of PBPs.

5.   Microorganisms develop an altered enzyme that can perform its metabolic function but is much less affected by the drug.

B. Origin of Drug Resistance. The origin of drug resistance may be genetic or nongenetic.

1. Genetic Origin of Drug Resistance. Most drug-resistant microorganisms emerge as a result of genetic change and subsequent selection processes by antimicrobial drugs. Genetic mechanism may be chromosomal or extra-chromosomal.

(i)     Chromosomal Resistance. Chromosome-mediated resistance occurs by spontaneous mutation in a locus that controls susceptibility to the drug. The antimicrobial drug serves as a selecting mechanism to suppress susceptible organisms and favor the growth of drug-resistant mutants. Spontaneous mutation is not a frequent cause of the clinical drug resistance in a given patient. But it occurs with high frequency to rifampicin. Mutation can result in the loss of PBPs, making such mutants resistant to a-Iactam drugs. Examples­Rifampicin, streptomycin, erythromycin. Resistance of M. tuberculosis to rifampicin is caused by mutation in RNA polymerase and that to isoniazid by mutation in catalase.

(ii)Extrachromosomal Resistance
(a)    Plasmid Resistance. This occurs by the extrachromosomal genetic elements called plasmid. Plasmid­mediated drug resistance is more common than that of chromosome. R factors (drug resistance plasmids) are a class of plasmids that carry genes for resistance to antimicrobial drugs. A single plasmid can carry genes that code for resistance to several drugs (multi-drug resistance -MDR) such as streptomycin, chloramphenicol, tetracycline and sulphonamides. Plasmid genes control the formation of enzymes capable of destroying the antimicrobial drugs, e.g. P­lactamases destroy P-lactam ring of penicillins and cephalosporins.

(b)  Transposon Resistance.
Genetic material responsible for antimicrobial resistance of a donor cell may be transferred to a sensitive recipient cell, and the recipient cell thus becomes resistant to the drug(s). The intercellular transfer of genetic material may occur by : (a) Conjugation, Conjugation is the most important of these mechanisms for the transfer of antimicrobial resistance. In most cases of conjugation the transferable DNA is plasmid, but chromosomal DNA may also be transferred, (b) Transduction. Transduction is the transfer of cell DNA by means of a bacterial virus (bacteriophage, phage). Transfer of gene for Beta lactamase production is mediated by bacteriophage, and (c) Transformation. It is a natural occurrence, and is a direct uptake of donor DNA by recipient cells.

2. Nongenetic Origin of Drug Resistance. This may be due to:
(i)    Metabolic inactivity. Most antibacterial drugs act when the microorganisms multiply actively. As such they become resistant to the drug when metabolically inactive, i.e. not multiplying. However, their offsprings are fully susceptible. Example: "Persisting" organisms like mycobacteria survive in tissues for many years after infection and do not multiply. They can not be eradicated by drugs. But if they start to multiply then they become fully susceptible to the same drugs.

(ii)  Loss of specific target structure. Microorganisms become resistant due to loss of a specific target structure. Example: During penicillin administration, penicillin-susceptible organisms may change to cell wall deficient L forms, and become resistant to cell wall-inhibitor drugs (penicillins, cephalosporins).

(iii)Infection at sites where antimicrobials are excluded or are not active.
NOTE: Examples:

A. Resistance to penicillins can be due to:
1.   Production of P-lactamases by staphylococci, gonococci, Gram-negative rods, and others. About 50 fl-lactamases are known and under the control of plasmids.
2.   Altered or lack of PBPs. Mostly under the control of chromosomes.
3.   Failure of activation of autolytic enzymes in cell wall.
4.   Failure to synthesize peptidoglycans, e.g. in L forms, mycoplasma.

B. Resistance to cephalosporins can be due to
1.   Poor permeation of bacteria by the drug
2.   Lack of PBP
3.   Degradation of drug by β-lactamases.

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