L23 - HIV Flashcards

1
Q

what is HIV

A

positive sense ssRNA retrovirus

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2
Q

what are endogenous retroviruses (HERVs)

A

ancient infections with retroviruses have implemnetd viral DNA into human genome

8% of human genome accounts for viral DNA

= most are inactive

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3
Q

what does HIV cause and which strain causes the most infections of this

A

AIDs

= Aquired Immunodefieiciency syndrome

HIV-1 - 40 milllion infected worldwide

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4
Q

what have we not been able to do to HIV

A

break the chain of transmission

= 40 million people living with HIV worldwide in 2021 - global pandemic

= 1.5 million new

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5
Q

where is HIV concentrated globally

A

South Africa

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6
Q

what is HIV split into

A

hierachical ranking

high abiulity to mutate = lots of strains/sub-types

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7
Q

source/ orogin of HIV-1 and HIV-2

A

HIV-1:

Simian Immunodefiecny virus (SIV) in primates recmobined to infect chimps

= SIVcpz
had the ability to infect humans

HIV-2:

SIV in ‘Sooty mangebey’ - SIVsmm

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8
Q

what was HIV orignally

A

Zoonotic infection

= primates harbor species specific SIVs

corss species transmission from hunting/butchering with blood contact

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9
Q

route of group M infection over history- HIV-1

A

originated in Congo

travelled to Haiti –> europe + America

= once it hit big cites like NYC and LA was hard to control

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10
Q

common fetsaures of retroviruses

A

Lipid envelope derived from host cell with glycoprteins imbeded

inner glycoprotein capsid maintains integrity

ssRNA —> placed in nucleus after retrotranscribing

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11
Q

3 defining enzymes of HIV/retroviruses

A

reverse transcriptase:
ssRNA —> dsRNA —dsDNA

integrase:
allows genteic material to be inserted into genome of host

protease:
cleaves transcibed viral proteins to mature them into functional proteins

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12
Q

simple replicative cyclke of HIV

A

binding to CD4 receptor by HIV on T-cells

chemokine receptor binds = comfrmational change and entry of virus

virus sheds shell and capsid

reverse transcriuptase –> ssRNA —> ssDNA

integrase places it within genome = cuts hsot DNA and inserts

viral proteins matured by protease and viral proteins bud and leave host cell

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13
Q

3 main regions of HIV genome

A

Pol (polymerase):
codes for enzymes

Gag (antigen):
codes for structural proteins to form viral particle

Env (envelope):
codes for envelope proteins involved in adhesion and entry

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14
Q

how does HIV spread round body

A

HIV invades and undegroes first repliaction

spreads to lymph nodes and invades immine cells

= used as ‘Trojan horses’ to get round body

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15
Q

relationship between CD4 t cell count over course of infection and HIV copies - AIDs

A
  1. HIV invades CD4 cells and numbers of them decline
  2. decline in hosts causes copies of HIV to decrease
  3. over course of years T-cell count gets lower and lower as HIV increases

= eventaul death due to opportunistic disease

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16
Q

dynamics of HIV replication on T cells

A

high tunover state leading to immune exhasution

= T-cells continously destroyed,produced and activated
= less effective over time

body is weakened when attacked by another infection = coesnt have the ability to fight it off

17
Q

AIDs vs HIV

A

condition vs prescence of pathogen

18
Q

which chemokine receptor does HIV bind to on T cells

19
Q

what can affect a persons succeptibility to AIDs

A

genetic variations
= some people are immune

CCR5 variations can affect binding to HIV

= depending on the mofifcations a person may have to CCR5

20
Q

antiretroviral therapy (ART)

A

target steps in HIVs life cycle

  • entry inhibitor
    reverse tarnscriptase inhibitor
  • integrase
  • protease

= combinations of these drugs can block progression

21
Q

timeline of proper ART prescription

A

1-6 months
= achieve undectable viral load

6 months +
= maintain undectable load

= No risk to transmitting to sexaul partner

22
Q

ARTs: PrEP vs PEP

A

PrEP:
Pre-Exposure Prophylaxis

= taking ARTs before being inected to prevent infection

PEP:
Post-exposure prophylaxis

= taking ARts after being exposed to HIV to prevent infection

23
Q

why is there no HIV vaccine yet

A

Suraface glycoproteins are variable and envelope constantly changes

High rate of mutation = tolerance for genetic diversity

lack of understanding what the ‘desired’ immune response is dfue to lack of people who survive

= elite controllers do not represent norm

24
Q

what are ‘elite controllers’ in terms of HIV

A

people who are able to control HIV infection without ART help

= we dont know why and this doesnt represent the norm

25
Q

disadvantages of ART

A

doesnt eliminate the virus just keeps it under control

expensive