Virus Replication Flashcards

1
Q

What is the step 0 of viral replication?

A

Entry into the body

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2
Q

What are 2 examples of entry points into the body (w/ virus)?

A
  • Respiratory; Influenza
  • Skin; arboviruses like Dengue
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3
Q

What are the steps of viral replication in order?

A

(0. Entry into body)
1. Attachment
2. Entry
3. Genome replication
4. Assembly
5. Egress

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4
Q

What is attachment?

A

Virus must bind to a compatible receptor to initiate infection

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5
Q

What are some examples of host receptors for viruses?

A
  • Proteins (e.g. CD4 for HIV)
  • Carbohydrates (e.g. siliac acid for Influenza)
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6
Q

What are some important features of the attachment stage?

A
  • Specificity: viral tropism is determined by presence of compatible receptor
  • Essentiality: viruses often bind to essential host molecules (hard for host to mutate away
  • Energy free: attachment is due to electrostatic attraction- difficult for cell to realise virus has bound
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7
Q

What are some examples of virus tropism due to attachment?

A
  • HIV-1 has a tropism towards CD4+ T cells, as it uses CD4 as a receptor (and CCR5/CXCR5 co-receptor)
  • Influenza has a tropism for respiratory epithelium, as cells there are lined with siliac acid (receptor)
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8
Q

What are 3 main cell entry mechanisms for viruses?

A

Direct penetration
Membrane fusion
Endocytosis

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9
Q

How does direct penetration work?

A

DNA is injected into the cell via a tail (e.g. by bacteriophage)

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10
Q

How does membrane fusion work?

A

Viral envelope fuses with plasma membrane.
Nucleocapsid of virus is released into the cytoplasm
Viral envelope stays as semi-circle on membrane (becomes a patch)

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11
Q

What is an example of a virus that enter via membrane fusion?

A

HIV

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12
Q

How does endocytosis work?

A

Virus particle is engulfed by host membrane, and forms endocytic vesicle
Low pH induces membrane fusion through changing structure around vesicle
Nucleocapsid is released into the cytoplasm

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13
Q

Which out of endocytosis and membrane fusion is pH independent?

A

Membrane fusion is pH independent

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14
Q

What is an example of a virus that enters via endocytosis?

A

Influenza.
Enters via Cathrin-mediated endocytosis

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15
Q

Does fusion occur in endocytosis?

A

Yes in some cases.
The difference is that the fusion occurs inside the endoscome, rather than the surface (like with membrane fusion entry).

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16
Q

For endocytosis, what allows fusion inside the endosome to occur?

A

Acidic endosomal pH triggers conformational change in fusion proteins, allowing fusion

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17
Q

What type of viruses undergo membrane fusion/endocytosis + fusion?

A

Enveloped viruses

18
Q

How do non-enveloped viruses typically enter cells?

A

Endocytosis + pore formation

19
Q

What is an example of a virus that undergoes endocytosis + pore formation?

A

Non enveloped viruses like Poliovirus & Adenovirus

20
Q

What is the main difference between endocytosis w/ fusion and endocytosis w/ pore formation?

A

In endocytosis w/ pore formation, capsid proteins undergo conformational changes inside the endosome which result in pore formation in the endosomal membrane.
Viral genome is then injected into the cytoplasm

21
Q

What happens during genome replication?

A

Various depending on Baltimore classification, however they all have one thing in common:
All viruses must make mRNA that is readable by host ribosomes (this is typically positive sense mRNA)

22
Q

Typically, what viruses can establish latency in their host?

A

DNA viruses (like Herpesviruses)

23
Q

What is the exception to DNA viruses establishing latency?

A

Retroviruses (like HIV), as they use reverse transcriptase and intergrase to integrate into host genome

24
Q

What is the assembly stage of viral replication?

A

Newly synthesised viral proteins and genomes are assembled into immature virions

25
Where does assembly occur?
Assembly can occur at different sites, including the nucleus, Golgi or ER membranes. Most viruses however will assemble at the plasma cell membrane
26
What often assists assembly?
Viral chaperones or scaffolding proteins
27
What are virions considered when they first assemble?
Immature (non-infectious)
28
What happens after the virions are assembled?
They must mature to become infectious. This can involve a different things for different viruses, including protease activity, capsid rearrangements or membrane acquisition
29
What are the 3 mechanisms of egress?
- Lysis - Budding - Exocytosis
30
What viruses use lysis?
- Non enveloped viruses (like Poliovirus)
31
What viruses use budding?
Enveloped viruses (like Influenza and HIV)
32
What viruses use exocytosis?
Some enveloped and some non-enveloped viruses
33
What is the impact of lysis?
Cell death; acute symptoms, highly inflammatory
34
What is the impact of budding?
Slow release, evasion of immune detection and persistent infections
35
What is the impact of exocytosis?
Preserves host cell for persistent infection
36
How does lysis work?
- Virus replicates until it overwhelms host - Often triggers apoptosis - Cell membrane bursts releasing virions
37
What is one reason why enveloped viruses don't exit via lysis?
They are enveloped so have a poorer environmental stability compared to non-enveloped
38
How does budding work?
Virion acquires host-derived lipid envelope containing viral glycoproteins, budding off from host membranes
39
What is an advantage of budding?
- Does not kill host cell (persistent infection) - Less inflammation - Acquired host envelope acts as camouflage from immune response
40
How does exocytosis work?
Virions are packaged into vesicles (e.g. from Golgi or ER) Vesicles move to cell surface and fuse with membrane, releasing virions