Lecture 3 Flashcards

1
Q

Three essential steps in viral replication

A
  1. Cell attachment and entry–> initiation of replication
  2. Production of viral components
  3. assembly and viral release
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2
Q

What is multiplicity of infection

A

1 infectious virus/cell

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3
Q

How to calculate plaque forming units (PFU/mL)

A

of plaques on plate/ volume of starting solution
or # of plaques on plate*dilution factor/volume plated

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4
Q

Where is the best place to block viral infection

A

Initiation of replication
-virus doesn’t get into cell in first place

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5
Q

How does virus do first step initiation of replication (attachment and replication)

A

Uses host cell receptors–>help attach
Receptors–>binding receptors changes conformation

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6
Q

What 2 things do viruses like HIV need to penetrate via membrane fusion

A
  1. Receptor->CD4
  2. Co-receptor->CCR5 or CXCR4
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7
Q

True or false: Immune cells with only 1 receptor are susceptible to virus infection

A

False: Immune cells with BOTH a receptor and co-receptor are susceptible to virus infection

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8
Q

What does it mean for the virus to be metastable or spring loaded

A

Unlocks energetic state that allows for fusion occur

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9
Q

How do enveloped viruses enter

A

Fuse through the membrane

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10
Q

How do non-enveloped viruses enter

A

1.Make a hole through membrane and delivers genome to cytoplasm
2. Lysis/kills cell & releases viral particles

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11
Q

What 2 ways can viruses enter?

A
  1. Cytoplasm
  2. Endocytosis
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12
Q

How does low pH trigger viruses to enter through endocytosis?

A

-Low pH signals virus that it is inside an intracellular location & that it should start penetration before it gets killed by phagocytosis–>low pH means phagocytosis will happen
-Low pH causes to virus structure to become metastable–>causes fusion

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13
Q

How does virus get to nucleus?

A

Viruses/viral components hitch rides around cell that leads to or close to nucleus by cytoskeletal network

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14
Q

How does virus get through nuclear membrane

A
  1. Waits for nuclear membrane to break down during cell division
  2. Partially disassemble in cytoplasm at nuclear pore
  3. Jam intact virion through nuclear pore
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15
Q

What type of polymerase do hosts use?

A

DNA dependent RNA polymerase

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16
Q

How do viruses make more than 1 protein?

A
  1. Multiple transcripts
  2. Alternative splicing
  3. Alternate start codons
17
Q

How does a polymerase that keeps falling off make multiple proteins

A

A single polymerase will fall off and restart at each gene creating multiple proteins

18
Q

What does protease do?

A

Cuts large polyprotein into functional pieces
-important for viral replication

19
Q

Why is inhibiting/stopping protease a main target for (+) RNA & HIV?

A

Stopping/inhibiting porteases stops viral infection since it cant replicate anymore

20
Q

Does virus need more capsid or protein?

A

Capsid

21
Q

Can viruses run through stop codons

A

yes, they can go past stop codon
-rare but can make extra proteins