lecture 7 Flashcards

1
Q

Replication of Viruses

A
  • do not have genetic capability to multiply by division
  • hijacks and utilizes host cell machinery to produce its proteins and nucleic acid for next generation of virus
  • process of virus replication in host cell resembles assembly line
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2
Q

permissive cell

A

cell is which a virus is able to replicate

the cell machinery supports replication of the virus

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3
Q

non-permissive cell

A

cells in which a factor or factors necessary to viral reproduction is not present or one detrimental to viral reproduction is absent

eg. absence of appropriate receptors

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4
Q

MOI (multiplicity of infection)

A

refers to the number of virions that are added per cell during infection

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5
Q

latent period

A

after uncoating and till just before 1st appearance and release of extracellular new virus particle

no extracellular virions detected

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6
Q

eclipse period

A

after uncoating and till just before first appearance of intracellular new virus progeny particles

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7
Q

adsorption

A

during this period virus attaches to and enters cell, titer of free virus in medium may decline

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8
Q

burst size

A

number of infectious virions released per average cell

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9
Q

virus attachment

A
  • attachment to receptor/s on host cells is/are very specific, lock and key like
  • each virus has its own specific receptor/receptors on specific host cells
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10
Q

attachment to the host cell surface

A
  • mediated by interaction between the virus and complimentary receptor on host cell surface, cell that lacks appropriate receptor escape being infected by virus
  • some cases, binding to cellular receptor is not sufficient for infection, additional cell surface molecule, or co-receptor required for entry
  • some viruses may use more than one host cell receptor, such as HIV
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11
Q

co-receptor

A

in some cases, binding to a cellular receptor is not sufficient for infection
-additional cell surface molecule, or co-receptor is required for entry

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12
Q

viruses can enter the host cell using any receptor present on surface of host cell

T/F

A

F

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13
Q

penetration /uncoating of non-enveloped/naked viruses

A
  1. receptor mediated endocytosis (commonly seen)

2. pore mediated penetration (in some naked viruses)

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14
Q

penetration and uncoating of enveloped viruses (depends on type of fusion protein)

A
  1. surface membrane fusion (have pH independent fusion protein)”
  2. receptor mediated endocytosis (have pH dependent fusion protein)
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15
Q

other/ uncommon methods of entry into host cell

A

-antibody- mediated attachment and penetration, as in FIPV

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16
Q

Virus penetration in many non-enveloped viruses

A

-Clathrin-mediated endocytosis or receptor-mediated endocytosis of virus by host

17
Q

less common virus penetration in non-enveloped viruses

A

pore-mediated penetration of viral genome into host cell

18
Q

surface membrane fusion of enveloped viruses

A
  • fusion of virus envelope with host cell membrane occurs directly on surface of host cell
  • facilitated by pH independent fusion protein
19
Q

receptor mediated endocytosis of enveloped viruses

A
  • pH dependent fusion protein
  • fusion of virus membrane with host endosomal membrane release viral genome
  • fusion protein requires low pH to be activated which is achieved in the endosome
20
Q

True/false antibody mediated attachment is used by viruses to penetrate the host cell

21
Q

virus uncoating

A
  • release of viral genome into the host cell

- virion can no longer be detected

22
Q

uncoating results in…..

A

loss of infectivity of virions

23
Q

functions of the parent virus in the host cell

A
  1. produce multiple copies of new viruses (children/progeny)
  2. produce viral proteins for capsid and successful replication
24
Q

reverse transcriptase

A

converts viral RNA to cDNA during virus replication

25
processing of primary RNA transcript (Pre-mRNA)
- viral mRNA must conform to requirements of host cell translation system i.e the host cell can recognize mRNA and translate - series of modification occurs known as processing of primary RNA transcript/pre-RNA - after processing mRNAs are translated into the cytoplasm - viral mRNAs produced in the nucleus must also be exported to the cytoplasm
26
processing of primary RNA transcript (Pre-mRNA)
1. capping 2. addition of 3' poly-adenylated tails 3. splicing
27
capping
-addition of 7-methylguanosine to the 5' end of RNA
28
RNA splicing
process which removes introns (non-coding region) and joins exons (coding region) in primary transcript
29
monocistronic mRNA
mRNA that encodes one polypeptide
30
polycistronic mRNA
mRNA encodes several polypeptides
31
assembly and maturation
- assembly of virus genome and proteins into new virions follow a specific order - all components, including nucleic acids and proteins, are packaged to form mature virions - may take place in nucleus, cytoplasm, plasma/ cell membrane (most enveloped viruses)
32
naked virions release progeny by....
lysis of host cell (cannot exit by budding because they lack envelope)
33
enveloped virions release progeny by....
budding through the plasma membrane
34
exocytosis
viruses that acquire envelope while budding from ER, golgi apparatus, or nuclear/nucleus membrane leave infected host cell by exocytosis
35
replication of retroviruses uses....
- reverse transcriptase (synthesizes RNA into DNA) | - integrase (integrates viral DNA to host genome)
36
viruses can acquire the lipid envelope only from the cell membrane of infected host cells? T/F
F
37
methods of cell-to-cell spread of viruses
1. extracellular spread 2. intercellular spread 3. nuclear spread of virus genome
38
intercellular spread
results in rapid virus dissemination, evasion of immune system, and persistent infections