General Principles of Virus Replication Flashcards

1
Q

What is the problem for negative-strand virus replication?

A

have to generate a copy strand
break dogma - no DNA step

carry polymerase molecules within the capsid

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2
Q

How do retroviruses replicate?

A

break central dogma
genome is reverse transcribed
virus particle packaged with necessary enzymes

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3
Q

How do simple positive strand RNA viruses replicate?

A

viral genome acts as mRNA
directly translated
all occurs in cytoplasm

organisation of coding regions within can vary

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4
Q

What is the overview of host cell protein synthesis?

A

eIF4F recognises 5’ cap structure
eIF4F recruits 43S ribosomal unit
43S scans mRNA until AUG then recruits 60S

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5
Q

What is another way of initiating translation?

A

IRES at 5’ end

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6
Q

What IRES elements are found at the 5’ end

A

poliovirus
rhinovirus
FMDV
Hepatitis C virus

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7
Q

What are RdRps?

A

RNA-dependent-RNA polymerases

only work in 5’ to 3’ direction

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8
Q

Do RdRps need a primer?

A

yes - to initiate replication

can be protein or RNA

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9
Q

How are RdRps error prone?

A

Quasi species

can result in viruses being inable to infect or are dead

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10
Q

Can saome viruses intiate transcription in the middle of the genome?

A

YES

can dose the material made

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11
Q

How does coronavirus replication have proof reading ability?

A

Nsp14
Nsp10
genome is large - need proof reading
still does mutate but a lot less

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12
Q

What is the multi protein complex of HCV?

A

structural and non structural
membrane associated regions
proteins NS3 NS4

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13
Q

What are virus replication factories?

A

provide physical scaffold to concentrate viral components - increase efficiency of replication

protects from cytoplasmic detectors

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14
Q

What is the ‘membranous web’

A

double membraned vesicles

concentrate replication components

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15
Q

Which cellular proteins are important for RNA replication?

A

PI4K - remodel lipids
PI4P

involved in membrane trafficking and curvature

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16
Q

What is the inhibitor of PI4K?

A

PIK93

17
Q

How can high resolution structure of 3Dpol fibrils of FMDV be determined?

A

cryo-EM microscopy

3D complex part of the replication factory