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2-3-10 Hive-1 Basic Virology and Pathobiology

1. HIV is a zoonosis transmitted from chimpanzees to humans around 1930. It has a lipid bilayer outer coating containing GP120 trimers and an inner capsid containing viral enzymes and genetic material. 2. HIV replicates by binding host cells via chemokine receptors and integrating its genetic material. It produces regulatory proteins that evade immune responses and inhibit host restriction factors. 3. HIV establishes chronic, low-level infection by infecting long-lived cells and resting CD4+ T-cells. Its high mutation rate allows drug resistance to emerge if replication is not fully suppressed. 4. HIV causes immune deficiency by depleting CD4+ T-cells, impairing immune function and

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0% found this document useful (0 votes)
54 views3 pages

2-3-10 Hive-1 Basic Virology and Pathobiology

1. HIV is a zoonosis transmitted from chimpanzees to humans around 1930. It has a lipid bilayer outer coating containing GP120 trimers and an inner capsid containing viral enzymes and genetic material. 2. HIV replicates by binding host cells via chemokine receptors and integrating its genetic material. It produces regulatory proteins that evade immune responses and inhibit host restriction factors. 3. HIV establishes chronic, low-level infection by infecting long-lived cells and resting CD4+ T-cells. Its high mutation rate allows drug resistance to emerge if replication is not fully suppressed. 4. HIV causes immune deficiency by depleting CD4+ T-cells, impairing immune function and

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2-3-10 HIV-1: Basic Virology and Pathobiology 1. Recognize HIV as a zoonosis from chimpanzees.

HIV is a zoonosis from chimpanzees !his "as decided #pon based on genome organization$ phylogenetic relatdness$ I%ing in the nat#ral host$ geographic coincidence$ and loo&ing at possible transmission ro#tes 'rosso(er to h#mans is belie(ed to be aro#nd 1)30 2. Describe HIV structure. !he o#termost coating of the (ir#s is a lipid bilayer that contains GP120 in trimer formation *the trimers are the acti(e attachment prod#ct !he inner coat is the capsid$ "hich contains P24 mar&ers +ithin the capsid are two sing e!stran"e" R#$s and three (ir#s specific enzymes *proteinase$ re%erse transcriptase$ and integrase, &. Describe the ife c'c e of HIV inc u"ing( Receptors on target ce s)*D4 an" **R+s !here are three different combinations of receptors on HIV$ "hich gi(es the (ir#s selective target cell tropism *different chemo&ine receptors target different cell types,: '%- . ''/0 -> binds macrophages '%- . '1'/- -> binds , ce s '%- . '1'/- or ''/0 -> binds , ce s !hese normal s#rface glycoproteins *'%-$ ''/23s$ and %'-4I56, are re7#ired for the f#nction of the ! cells and macrophages8 !h#s$ host cells are complicit in HIV infection Virus!specific enz'me functions)re%erse transcriptase- integrase- protease /e(erse transcriptase mediates the synthesis of pro(iral %69 from the HIV ss/69 genome Integrase integrates that pro(ir#s into the host cell genome Protease clea(es polyproteins into indi(id#al f#nctional HIV proteins and enzymes :or e;ample$ it clea(es en( polyprotein gp1<0 into en(elope glycoproteins gp120 and gp-1 Virus!specific regu ator' proteins $P./0*&: family of n#cleic acid editing enzymes that deaminates '= in retro(iral c%69 and ind#ces fatal m#tations HIV Vif binds and inhibits $P./0*& in humans ,RI123 is a cytoplasmic body component that restricts HIV infection in other primates$ pre(enting capsid shedding and release of (iral %69 ,etherin 4*D&156 inhibits HIV release from infected cells$ "hile HIV Vp# inhibits tethering acti(ity !heternin-mediated HIV retention refers to the ability of b#dded HIV (ir#s to be ta&en #p by the host cell again 4. .ut ine HIV rep ication "'namics an" its re ationship to the persistence of infection an" the emergence of "rug resistance.

HIV replication dynamics: 9c#te phase Imm#ne competence drops rapidly "ith primary infection to near the disease threshold !hen the platea#-phase infection *chronic phase, happens 'hronic phase 9bo#t 10 million (ir#s particles are made per day$ b#t most are eliminated !he half life of free (ir#s in plasma is less than 2 ho#rs and can be eliminated in 2 "ee&s In addition$ abo#t 1 billion '%-> ! cells are eliminated daily$ b#t most are resplaced 9cti(ated '%-> ! cells are the primary so#rce and target of free (ir#s ?Prod#cti(ely-infected@ cells ha(e a half life of 2 days and can be eliminated in 1 month If a retarded doctor *or non-compliant patient, administers a single dr#g treatment$ "ild type (ir#s con(erts to dr#g-resistant (ir#s after A#st 1- days8 !here are also ?long-li(ed@ infected ! cells that ha(e a 1-- "ee& half-life$ and ta&e 2-0 years to eliminate Bastly$ there are resting '%-> !-cells that ha(e half-li(es of months$ and ta&e decades to eliminate Cmergence of dr#g resistance: 4pontaneo#s n#cleic acid m#tation arises d#ring (iral replication and res#lts in 99 s#bstit#tions in (iral proteins !he extraordinary replication rate and lack of nucleic acid repair res#lts in a high m#tation rate !he res#ltant 99 s#bstit#tions target enzyme a(idity for indi(id#al dr#g inhibitors of enzyme f#nction !h#s$ complete s#ppression of (iral replication is re7#ired to pre(ent resistance 2. I"entif' properties of HIV that are associate" with immune e%asion an" immune "eficienc'. 6ot all HIV3s are e7#al$ d#e to their high mutation rate and mar&ed genomic (ariability HIV imm#ne e(asion: Preferential infection of HIV specific '%- ! cells /ed#ction in '%- ! cell f#nction Dacrophages archi(e HIV (irions HIV ma&es reg#latory gene prod#cts thatE Vpr: s#ppresses IB-12 prod#ction from macrophages Vif: inhibits 9PFBC'3 #ef: red#ces '%- e;pression and bloc&s apoptosis Vpu: inhibits tethering and 6G! cell acti(ation 7. Describe current concepts of HIV "isease pathogenesis. HIV-ind#ced Imm#ne %eficiency /apid early destr#ction of 00H of m#cosal memorty ! cells888

'%-> ! cells are depleted by "irect c'toto8icit'$ s'nc'tia formation$ and innocent b'stan"er effects %ecreased BD prod#ction of lymphoid prec#rsors %ecreased thymic o#tp#t of ne" ! cells *"ill see disr#pted thymic and lymph node architect#re, Carly se7#estration of '%-> ! cells in B63s Bater destr#ction of B6 architect#reimpaired clonal e;pansion 6H399 of gp-1 interferes "ith lipid rafts and ! cell acti(ation

!he pathophysiology of HIV can be simplified to as follo"s: HIV ca#ses cell deficiencyIdysf#nctionopport#nistic infections HIV infects '64 Dicrogliane#roencephalopathy InappropriateI#ncontrolled imm#ne acti(ationproliferati(e disorders *BIP*lymphocytic interstitial pne#monia,$ adenopathy$ hepatosplenomegaly, and systemic cyto&ine effects *fatig#e$ "asting,

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