Virus Replication Flashcards

1
Q

What determines the pathogenic potential and tropism of a virus?

A

Identity, location, density, and function or cell receptors and attachment factors

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What are cell receptors?

A

Receptors on the cell membrane that have a normal function for the cell. Provide a place for viral attachment. Viruses evolve to attach the receptors for entry.

May send signals that attract viruses

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What are attachment factors?

A

less specific

do not promote virus attachement via signals

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Steps of virus entry (5)

A
  1. Bind via receptors, attachment factors, co-receptors
  2. Signal, conformation changes, fusion or internalization
  3. Transport to endosomes
  4. Release from endosome via cures such as low pH
  5. Transport to cytosol or nuclues - uncaring of nucleic acids
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

How do receptors bind to virus?

A

Viral envelope
* glycoprotein attachment

Non enveloped

  • attach to protein projections directly from capsid
  • attach to “canyons” of the capsid
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Once virus is attached to receptor what can occur?

A

May trigger fusion or other steps for entry
May send cellular signals enhancing viral entry and infection
Co-receptors may bind and cause secondary changes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What can occur if virus attaches to attachment factors?

A

Proteoglycans help concentrate visions on cell surface and increase efficiency

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Movement of viruses outside of the cell

A

FILOPODIA - help translocate the virus to find a receptor

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Movement of viruses inside the cell

A

ACTIN and MICROTUBULE machinery

*nuclear or cytoplasmic

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Endocytosis is used for virus entry. Why is this beneficial?

A

Virus fuse directly with plasma membrane

  • free ride to nucleus (cytoplasm is crowded)
  • Doesn’t leave traces for immune detection
  • Multiple pathways - allows flexibility and more tropism
  • use cell signals in endosome (low pH) to facilitate uncoating and release
  • virus can trigger macropinocytosis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

How does a virus get out of the endosome?

A

Enveloped viruses:

  • fuse with membrane and release into cytosol
  • change acid content creates membrane permeability

Nonenveloped:
* penetrate the vesicle membrane by puncture, perforation, or lysis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What is the NPC?

A

Nuclear pore complex

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

How do viruses get genomic material into nucleus?

A

Through the NPC - different viruses achieve this differently

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

RNA viruses enter nucleus how?

A

Do not have a capsid

** will enter directly through the NPC **

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Hepadnaviridae enters nucleus how?

A

capsid enters NPC but remains attached to it and releases the viral genomic DNA into the nucleoplasm

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

ssDNA virus enters how?

A

capsizes are small enough to cross NPS and enter nucleus with intact capsid – will release from capsid inside nucleus

17
Q

Herpesvirales capsid enters how?

A

Too large to enter NPC – viral genome is directly injected through NPC

18
Q

Retroviruses enter how?

A

during mitosis with the nuclear membrane is degraded

19
Q

Obstacles for replicating viral genome (4)

A

which polymerase
where to replicate
how to transcribe to make mRNA
how to generate protein in the right proportions at the right time

** these can lead to targets for drug therapy **

20
Q

dsDNA viruses use _____ DNA polymerase or ____ ____ ____

A

cellular
make their own

    • HERPES
    • PAPILLOMA
    • POLYOMA
21
Q

ssDNA first replicate their DNA using _____ DNA polymerase

A

cellular

    • PARVO
    • ANELLO
    • CIRCO
22
Q

some dsDNA make their own ______ transcriptase

A

virion

** POX

23
Q

Viruses that use cellular RNA polymerase or cellular DNA polymerase are easier or harder to target for treatment?

A

Harder - pose toxicity to the host

24
Q

+ strand RNA viruses make protein _______ from their genome

A

Directly

  • genome acts as mRNA
25
Q
  • strand viruses must make ___ ________ RNA polymerases to make mRNA
A

RNA dependent

26
Q

Retroviruses must ______ transcribe their RNA and use ____ RNA polymerase

A

Reverse

Cellular

27
Q

DNA viruses that use host DNA polymerases …..

A

fully dependent on host functions.

transport nucleus to replicate their DNA and transcribe mRNA

28
Q

DNA viruses that make their own DNA polymerase and a whole replication complex….

A

Make special transcription factors to preferentially transcribe their genes.

  • carefully controlled
    * immediate early
    * early
    * late

Viruses that can replicate in the nucleus can splice genes! Rearrange to make special combinations - doesn’t wast resources

** HERPES

29
Q

Herpes

A

Latent and Lytic stages
* latent:
the virus exists as a plasmid - bound to chromosome
replicated passively by host DNA replication
restricted –

  • lytic
    linear genomes are produced by rolling circle mechanism
30
Q

+ strand RNA replicate in the CYTOPLASM

A

produce + and - strands

multigened mRNA is translated into polyprotein – cleaved into separate proteins

31
Q
  • strand ssRNA virus replication
A

occurs in the NUCLEUS
RNA dependent RNA polyermase (creates an RNA template from RNA)
Antigenote is used for both translation and as a replication template
* coated to prevent translation when used as a template for replication