Virology: Chapter 2 Flashcards

(50 cards)

1
Q

Explain the process of adsorption and attachment

A

Adsorption = initial contact
so the virus bumps into the host cell via random collisions, doesn’t need energy

Attachment = specific binding
protein on the surface binds to the virus receptor

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2
Q

Host range

A

Are what cells the virus can infect
cells = that have receptors!
determined by
- receptor in the cells
- intracellular factors needed to replicate

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3
Q

Narrow Host Range

A

Very specific
HIV: CD4 protein which are specific immune cells

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4
Q

Wide Host Range

A

Very broad
Measles: CD60 protein which are found most human cells

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5
Q

Susceptible

A

cell has the receptor = virus can bind and enter their genome

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6
Q

Permissible

A

cell has the correct machinery for the viral genome to replicate and produce progeny virus

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7
Q

How can we prevent viruses from attaching to the cells

A

Vaccines
- induce the production of neutralizing antibodies that bind to the anti-receptors so the virus can’t bind

Block Host Cell Receptor
- use antibodies to block virus receptor
e.g SARS COV 19 = ACE-2 receptors

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8
Q

What is the disadvantage of blocking ACE-2 receptors?

A

that receptor is important for cell functions like regulating blood pressure, so if you block it (so covid cannot bind), there will be side effects

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9
Q

Is Genome Entry energy dependent?

A

Yes. it uses energy

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10
Q

What are the 4 ways a genome can enter a host cell?

A
  1. Endocytosis + Uncoating
  2. Endocytosis + Pore Formation
  3. Endocytosis + Membrane Fusion (ENVELOPE only)
  4. Direct Membrane Fusion (ENVELOPE only)
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11
Q

Endocytosis + Uncoating

A

virus binds, form endosome, endosome take virus into the cell, capsid breaks, genome enters cytoplasm

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12
Q

Endocytosis + Pore Formation

A

virus binds, endosome takes virus into the cell. virus forms a pore in endosome membrane, genome pass through pore

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13
Q

Endocytosis + Membrane Fusion (ENVELOPED ONLY)

A

virus binds, endosome takes it into the cells, virus ENVELOPE fuses with endosome membrane, genome released

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14
Q

Direct Membrane Fusion (ENVELOPED ONLY)

A

virus binds and directly fuses with the host cell’s plasma membrane, genome enters

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15
Q

Genome Replication and Expression has 2 functions, which are

A
  • genome used as a template to make more genome copies, more progeny virus
  • genome used to make viral mRNA to make viral protein
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16
Q

What are some limitations that a host cell presents to a virus with regards to its replication (2)

A
  • not the right virus receptor = can’t attach
  • not the right enzymes / host factors = virus can’t replicate
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17
Q

Can a cell be susceptible but not permissive? Can a cell be resistant to a viral infection, yet be permissive to viral infection?

A

YES

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18
Q

Do viruses make their own amino acids and nucleotides during replication?

A

NO, its NOT independent

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19
Q

Do viruses use their host cell’s ribosomes?

A

YES

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20
Q

What does host cell RNA Pol. do?

A

read DNA template from 3’ to 5’, and synthesize from 5’ to 3’

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21
Q

Ribosome translate (+) mRNA from

22
Q

All virus genomes are surrounded by proteins called…

23
Q

function of the capsid

A

PROTECT AND DELIVER
protect the genome from:
- nucleases in environment
- damaging agents
- mechanical force

deliver virus genome to the location of replication and expression in the host cell

24
Q

why does the capsid must be stable enough yet unstable enough

A

stable enough to protect, unstable enough to be broken down so genome can be released

25
What type of interactions exist between proteins and subunits of the capsid
protein-protein interactions that cause conformational change to the capsid so genome can be released
26
What might cause capsid to change from a stable to unstable structure
cut, pH, heat
27
Explain the relation between DNA virus and the cell cycle replication in regards to permissiveness
if cell cycle is in G1, the DNA is still growing, so the host cell is not permissive if cell cycle is in S, the DNA is synthesized, so the host cell is permissive
28
Explain why RBC are never permissive
because they lack a nucleus, so they cannot make amino acids, virus can't replicate
29
Explain why mouse cells are permissive, but NOT susceptible to Polio, making them NOT resistant
because you can inject polio (RNA virus) to the cytoplasm and the virus can replicate, but the mouse cell doesn't have the right receptors for the virus to bind and enter naturally
30
Why do naked viruses survive longer in the environment? and are more virulent?
Because they just have a protein capsid, and they cause cell lysis (so host cell die)
31
Why are enveloped viruses more fragile and sensitive, and less virulent?
Because they're lipid bilayer is fragile and sensitive to pH and heat, so they break easily, making the virus less stable, and less virulent and they don't always cause cell lysis, they sometimes bud.
32
Why some viruses package their own replicative enzymes in their capsid?
Because some viruses replicate in the cytoplasm so they cannot access the host cells DNA/RNA Polymerase because they're in the nucleus
33
Why do RNA viruses use RDRP (like they encode they're own enzyme no matter the location)
because host cell RNA Pol doesn't read RNA template, they read DNA template
34
RNA and DNA virus can replicate in...
cytoplasm or nucleus
35
if DNA virus replicates in the nucleus, then they use DNA / RNA Pol of the
host cell
36
if DNA virus replicate in the cytoplasm, then the virus genome use DNA / RNA pol of the..
virus itself (code by itself) so the capsid contains pre-made pol
37
RNA viruses encode what enzyme
RDRP
38
RNA viruses only have pre-made RNA pol IN THEIR CAPSID only if...
RNA is (-) stranded
39
If the RNA (+) strand (RNA virus) then
the virus will make RNA pol AFTER infecting the cell, not pre-made
40
Retrovirus pathway of genome replication and expression
RNA --> ss RNA --> ds DNA ---> ss RNA
41
what enzyme retrovirus uses to transcribe ssRNA to dsDNA
RT
42
Advantages of a retrovirus
use cell's RNA Pol and integrate into the cell genome making it hella dangerous
43
if viral mRNA doesn't have a 5'cap, it uses
a secondary structure
44
viral mRNA can be monocistronic and polycistronic, why are polycistronic viral mRNA's not good at translation
because the ribosomes would read one gene and then stop
45
so what's the strategy to overcome this
translate entire mRNA into polyprotein and then cut it up into individual proteins (capsid, rdrp, etc)
46
(+) double stranded nucleic acid
same sequence as mRNA
47
(-) double stranded nucleic acid
template for making (+) strand
48
the (+) and (-) ds are...
complementary
49
For ss RNA viruses (+) strand RNA...
has the coding sequence and can be translated directly by host ribosomes it still must be transcribed to synthesize mRNA (+) --> (-) ---> (+)
50
For ss RNA viruses (-) strand RNA...
can't be directly translated, must be transcribed to make a complementary (+) strand that acts as mRNA