Chapter 5 Flashcards

1
Q

Why have viruses been termed parasites?

A

Because viruses must depend on, and take over, the host cell for the majority of their metabolic and biosynthetic reactions

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

Define susceptiible in the context of virus-cell interactions.

A

The cell is sensitive to infection by a particular virus, Largely a function of the presence or absence of receptors. Does not necessarily imply productive infection.

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

Define permissive in the context of virus-cell interactions.

A

Cell is able to support complete replication of a particular virus. This is a function of the internal biochemistry of the cell, not the presence or absence of receptors.

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

Define productive in the context of virus-cell interactions.

A

An infection of a cell by a virus that results in the production of progeny virions.

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

Define cytocidal in the context of virus-cell interactions.

A

Virus replication results in damage to cell, resulting in death of the cell

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Define persistent in the context of virus-cell interactions.

A

virus infection that lasts a long time - infection is lasting beyond the time when the immune system might be reasonably expected to clear the infection

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

Define latent.

A

Virus infection in which viral genome is maintained, but few viral gene products are made and no virus is produced.

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

Define inclusion bodies.

A

They may be viral components or the result of virus-induced degenerative changes - their occurance in tissues demonstrates the presence of a virus infection.

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

What can inclusion bodies be (morphology/location)?

A

They may be intranuclear or intracytoplasmic, single or multiple, large or small, acidophilic or basophilic

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

What is a lytic infection?

A

alteration in the cell leading to cell death

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What is a non-lytic infection?

A

When there is a persistent infection wherein virus production coexists within the cell without dramatically altering it - when there is little or no visible cell alteration in cell, little metabolic damage, cell division continues, and there may be loss of specialized functions

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

Define oncogene.

A

cellular or viral gene whose products are able to transform eukaryotic cells so that they begin to grow like tumor cells

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

What is a proto-oncogene?

A

A gene that is normally switched off gets switched on under influence by the virus; it gives rise to v-onc in a transforming virus

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

Define transduction.

A

transfer by a virus of cellular genes from one organism or cell to another

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

Explain the basis for the transforming ability to Rous sarcoma virus.

A

It is a strongly transforming retrovirus because an oncogene is inserted but does not replace the viral genes, so the virus is still capable of replicating with the addition of the oncogene

Usually when an oncogene is added some of the virus’ genes are replaced and it can no longer replicate. It is not the case here

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

Explain what insertional activation by cis-activating retroviruses means.

A

Oncogenic retriviruses that activate normal cellular oncogenes by integrating near them. The retrovirus integrates in the vicinity of a cellular oncogene. This places the regulation under the control of the transcriptional regulatory elements in the viral LTR sequences.

17
Q

Give 2 examples of trans-activating retroviruses.

A

bovine leukemia virus and human T-cell leukemia viruses

18
Q

What DNA viruses are not capable of oncocogenic transformation?

A

parvoviruses - they are so small and their genomes contain so few genes that they cannot code for the ‘early’ proteins necessary to set the cell up for viral replication

19
Q

What is a cytopathic effect?

A

a virus-induced cellular change that are visible by light microscopy

20
Q

What are the cytopathic effects that were mentioned in class?

A

cell lysis, syncytial cell formation, and inclusion bodies

21
Q

What is a tumor supressor gene?

A

a gene whose product negatively regulates the cell cycle and if mutated or inactivated can lead to rapid cell division and transformation