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Microbiology 1st Edition Wessner Test Bank
Microbiology 1st Edition Wessner Test Bank
Microbiology 1st Edition Wessner Test Bank
Bank
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Package Title: Wessner Testbank
Course Title: Microbiology WileyPLUS
Chapter Number 8
Answer: d
Difficulty: Easy
Learning Objective: LO 8.1 Explain how viruses recognize and attach to host cells, and how this
system determines the host range.
Section Reference: Sec 8.1 Recognition of Host Cells
2) The viral attachment protein specifically binds to a host cell receptor. All of the following are
examples of known host cell receptors except
a) DNA.
b) proteins.
c) glycoproteins.
d) lipopolysaccharides.
e) sialic acids.
Answer: a
Difficulty: Medium
Learning Objective: LO 8.1 Explain how viruses recognize and attach to host cells, and how this
system determines the host range.
Section Reference: Sec 8.1 Recognition of Host Cells
3) The ability of a virus or bacteriophage to specifically attach to a host cell occurs through the
interactions of the viral attachment protein with the host cell receptor. This binding determines
Answer: b
Difficulty: Easy
Learning Objective: LO 8.1 Explain how viruses recognize and attach to host cells, and how this
system determines the host range.
Section Reference: Sec 8.1 Recognition of Host Cells
4) E. coli strain K12 is susceptible to infection by phage T2. T2 binds to K12 via two attachment
proteins. These two proteins specifically bind to the following two host cell receptor proteins
found on the surface of strain K12.
Answer: c
Difficulty: Medium
Learning Objective: LO 8.1 Explain how viruses recognize and attach to host cells, and how this
system determines the host range.
Section Reference: Sec 8.1 Recognition of Host Cells
a) binding nucleic acid polymerases and preventing viral nucleic acid replication.
b) binding ribosomes and preventing viral protein translation.
c) activating macrophages to phagocytize the virus.
d) binding to the viral attachment proteins to prevent attachment to the host cell receptor.
e) binding to the host cell receptor molecule to prevent the attachment of the virus.
Answer: d
Difficulty: Medium
Learning Objective: LO 8.1 Explain how viruses recognize and attach to host cells, and how this
system determines the host range.
Section Reference: Sec 8.1 Recognition of Host Cells
6) Antiviral drugs that act at the level of host recognition are designed to
Answer: b
Difficulty: Medium
Learning Objective: LO 8.1 Explain how viruses recognize and attach to host cells, and how this
system determines the host range.
Section Reference: Sec 8.1 Recognition of Host Cells
7) The second step in viral replication is entry. For bacteriophage, entry usually involves
a) phagocytosis.
b) receptor-mediated endocytosis.
c) direct entry of the nucleic acid into the cell.
d) membrane fusion mechanism of entry.
e) digestion of the peptidoglycan.
Answer: c
Difficulty: Easy
Learning Objective: LO 8.2 Describe the processes by which enveloped or non-enveloped
viruses may enter a cell.
Section Reference: Sec 8.2 Viral Entry and Uncoating
a) phagocytic
b) receptor-mediated endocytotic
c) membrane fusion
d) acid-dependent endosomal
e) receptor-independent endocytotic
Answer: c
Difficulty: Easy
Learning Objective: LO 8.2 Describe the processes by which enveloped or non-enveloped
viruses may enter a cell.
Section Reference: Sec 8.2 Viral Entry and Uncoating
9) The influenza virus gains entry into a host cell by
Answer: d
Difficulty: Medium
Learning Objective: LO 8.2 Describe the processes by which enveloped or non-enveloped
viruses may enter a cell.
Section Reference: Sec 8.2 Viral Entry and Uncoating
10) The influenza virus gains entry into a host cell by an endocytotic process. The viral
nucleocapsid leaves the endosome and enters the cytoplasm through a membrane fusion
mechanism. Fusion of the viral envelope with the endosomal membrane is facilitated by
Answer: a
Difficulty: Medium
Learning Objective: LO 8.2 Describe the processes by which enveloped or non-enveloped
viruses may enter a cell.
Section Reference: Sec 8.2 Viral Entry and Uncoating
a) membrane fusion.
b) pinocytosis.
c) injection of nucleic acid into host cell.
d) lysis of host cell membrane.
e) receptor mediated endocytosis.
Answer: e
Difficulty: Easy
Learning Objective: LO 8.2 Describe the processes by which enveloped or non-enveloped
viruses may enter a cell.
Section Reference: Sec 8.2 Viral Entry and Uncoating
12) Most non-enveloped viruses enter the host cell by receptor-mediated endocytosis. The virus
or its nucleic acid is able to leave the endosome and enter the cytoplasm
Answer: d
Difficulty: Medium
Learning Objective: LO 8.2 Describe the processes by which enveloped or non-enveloped
viruses may enter a cell.
Section Reference: Sec 8.2 Viral Entry and Uncoating
Answer: b
Difficulty: Easy
Learning Objective: LO 8.2 Describe the processes by which enveloped or non-enveloped
viruses may enter a cell.
Section Reference: Sec 8.2 Viral Entry and Uncoating
14) Fuzeon is an antiviral drug that prevents membrane fusion for entry into the cell by HIV. The
mode of action for this drug is
Difficulty: Medium
Learning Objective: LO 8.2 Describe the processes by which enveloped or non-enveloped
viruses may enter a cell.
Section Reference: Sec 8.2 Viral Entry and Uncoating
15) The Baltimore classification scheme for viruses divides all viruses into seven groups based
on
Answer: c
Difficulty: Easy
Learning Objective: LO 8.3 Identify the seven classes of virus, explaining how the classification
system is based on their replication system.
Section Reference: Sec 8.3 Viral Replication Strategies
16) The Baltimore classification scheme classifies viruses based on their mechanism of mRNA
synthesis. Using this classification scheme, all viruses are placed into ______ classes.
a) seven
b) five
c) four
d) ten
e) twenty five
Answer: a
Difficulty: Easy
Learning Objective: LO 8.3 Identify the seven classes of virus, explaining how the classification
system is based on their replication system.
Section Reference: Sec 8.3 Viral Replication Strategies
17) Class I viruses, double-stranded DNA viruses, usually utilize the following polymerases for
mRNA synthesis and DNA replication
a) host cell DNA-dependent RNA polymerase and host cell DNA-dependent DNA polymerase.
b) viral DNA-dependent RNA polymerase and viral DNA-dependent DNA polymerase.
c) viral RNA-dependent RNA polymerase and host cell DNA-dependent DNA polymerase.
d) host cell RNA-dependent RNA polymerase and host cell DNA-dependent DNA polymerase.
e) viral RNA-dependent RNA polymerase and viral DNA-dependent DNA polymerase.
Answer: a
Difficulty: Medium
Learning Objective: LO 8.3 Identify the seven classes of virus, explaining how the classification
system is based on their replication system.
Section Reference: Sec 8.3 Viral Replication Strategies
18) Class III viruses, double-stranded RNA viruses, utilize the following polymerase for genome
synthesis
Answer: c
Difficulty: Easy
Learning Objective: LO 8.3 Identify the seven classes of virus, explaining how the classification
system is based on their replication system.
Section Reference: Sec 8.3 Viral Replication Strategies
19) Class V viruses, negative sense single-stranded RNA viruses, utilize the following
polymerase for mRNA synthesis
Answer: d
Difficulty: Easy
Learning Objective: LO 8.3 Identify the seven classes of virus, explaining how the classification
system is based on their replication system.
Section Reference: Sec 8.3 Viral Replication Strategies
20) Class VII viruses, double-stranded DNA viruses that utilize reverse transcriptase, replicate
their genome using the following polymerase
Answer: e
Difficulty: Medium
Learning Objective: LO 8.3 Identify the seven classes of virus, explaining how the classification
system is based on their replication system.
Section Reference: Sec 8.3 Viral Replication Strategies
21) For most double-stranded DNA eukaryal viruses, DNA replication occurs in the _________
and translation occurs in the __________.
a) cytoplasm, cytoplasm
b) cytoplasm, nucleus
c) nucleus, nucleus
d) nucleus, cytoplasm
e) mitochondria, cytoplasm
Answer: d
Difficulty: Easy
Learning Objective: LO 8.3 Identify the seven classes of virus, explaining how the classification
system is based on their replication system.
Section Reference: Sec 8.3 Viral Replication Strategies
Answer: a
Difficulty: Medium
Learning Objective: LO 8.3 Identify the seven classes of virus, explaining how the classification
system is based on their replication system.
Section Reference: Sec 8.3 Viral Replication Strategies
23) A bacteriophage genome that is integrated into the bacterial chromosome is called
a) a prophage.
b) a virulent phage.
c) a transforming phage.
d) a genome phage.
Answer: a
Difficulty: Easy
Learning Objective: LO 8.3 Identify the seven classes of virus, explaining how the classification
system is based on their replication system.
Section Reference: Sec 8.3 Viral Replication Strategies
24) Phage lambda (λ) is referred to as a temperate phage. What is a temperate phage?
Answer: d
Difficulty: Easy
Learning Objective: LO 8.3 Identify the seven classes of virus, explaining how the classification
system is based on their replication system.
Section Reference: Sec 8.3 Viral Replication Strategies
25) Protease inhibitors are routinely used in the treatment of an HIV infection to slow down the
progression of the disease. How do these inhibitors work?
a) They inhibit the process of translation for the production of viral proteins.
b) They inhibit the process of entry by interacting with the fusion peptide.
c) They block the attachment process by interacting with the viral attachment protein.
d) They inhibit the proteolytic modification of the viral capsid to form an infectious virion.
e) They inhibit the activity of the viral enzyme reverse transcriptase.
Answer: d
Difficulty: Medium
Learning Objective: LO 8.4 Explain how new viral particles assemble within the infected host
cell, describing the different processes involved in the egress of these newly created viruses from
the cell.
Section Reference: Sec 8.4 Viral Assembly and Egress
26) Most enveloped viruses exit the cell by the following process
a) exocytosis.
b) budding.
c) Golgi transport.
d) cell lysis.
e) cytokinesis.
Answer: b
Difficulty: Easy
Learning Objective: LO 8.4 Explain how new viral particles assemble within the infected host
cell, describing the different processes involved in the egress of these newly created viruses from
the cell.
Section Reference: Sec 8.4 Viral Assembly and Egress
27) Most non-enveloped viruses exit the cell by the following process
a) exocytosis.
b) budding.
c) Golgi transport.
d) cell lysis.
e) cytokinesis.
Answer: d
Difficulty: Easy
Learning Objective: LO 8.4 Explain how new viral particles assemble within the infected host
cell, describing the different processes involved in the egress of these newly created viruses from
the cell.
Section Reference: Sec 8.4 Viral Assembly and Egress
28) The intact virion of the tobacco mosaic virus is assembled by this method
a) the capsid is first assembled and the nucleic acid is packaged into the capsid.
b) part of the capsid is assembled and the nucleic acid is packaged into the capsid.
c) the capsid proteins assemble around the viral nucleic acid.
d) the nucleic acid is inserted into the cell membrane and the capsid acquires the nucleic acid as
it buds through the membrane,
e) the capsid is assembled in the cytoplasm and the nucleic acid is packaged in the nucleus.
Answer: c
Difficulty: Medium
Learning Objective: LO 8.4 Explain how new viral particles assemble within the infected host
cell, describing the different processes involved in the egress of these newly created viruses from
the cell.
Section Reference: Sec 8.4 Viral Assembly and Egress
29) Bacteriophage T4 lyses the bacterial host cell for release of newly formed virions. The cell
wall of the bacterium is broken down by this virally encoded enzyme
a) lysozyme.
b) protease.
c) β-lactamase.
d) nuclease.
e) peptidase.
Answer: a
Difficulty: Easy
Learning Objective: LO 8.4 Explain how new viral particles assemble within the infected host
cell, describing the different processes involved in the egress of these newly created viruses from
the cell.
Section Reference: Sec 8.4 Viral Assembly and Egress
30) Which of the following viral replication processes would not be a good target for an antiviral
drug?
a) Attachment
b) Viral entry
c) Translation of viral proteins
d) Uncoating of viral capsid
e) Assembly of virus capsid
Answer: c
Difficulty: Easy
Learning Objective: LO 8.5 Identify several antiviral drugs and the virus-specific processes that
they target.
Section Reference: Sec 8.5 Antiviral Agents
31) Many antiviral drugs are nucleoside analogs. The nucleoside analogs primarily target these
enzymes
Answer: d
Difficulty: Easy
Learning Objective: LO 8.5 Identify several antiviral drugs and the virus-specific processes that
they target.
Section Reference: Sec 8.5 Antiviral Agents
32) The reason nucleoside analogs are effective against viral nucleic acid polymerases is because
Answer: c
Difficulty: Easy
Learning Objective: LO 8.5 Identify several antiviral drugs and the virus-specific processes that
they target.
Section Reference: Sec 8.5 Antiviral Agents
a) herpes virus.
b) HIV.
c) papilloma virus.
d) influenza virus.
e) polio virus.
Answer: b
Difficulty: Easy
Learning Objective: LO 8.5 Identify several antiviral drugs and the virus-specific processes that
they target.
Section Reference: Sec 8.5 Antiviral Agents
34) The enzyme _______ has a high affinity for AZT and will incorporate it into a newly
synthesized DNA strand. This will effectively terminate DNA replication because the incoming
nucleotide cannot be bound to AZT.
Answer: b
Difficulty: Easy
Learning Objective: LO 8.5 Identify several antiviral drugs and the virus-specific processes that
they target.
Section Reference: Sec 8.5 Antiviral Agents
35) An HIV mutant has been identified that is resistant to the drug AZT. Most likely the
mutation occurred in the viral gene that encodes for
Answer: c
Difficulty: Medium
Learning Objective: LO 8.5 Identify several antiviral drugs and the virus-specific processes that
they target.
Section Reference: Sec 8.5 Antiviral Agents
36) The main function of a host cell receptor is to specifically bind to the viral attachment
protein.
Answer: False
Difficulty: Easy
Learning Objective: LO 8.1 Explain how viruses recognize and attach to host cells, and how this
system determines the host range.
Section Reference: Sec 8.1 Recognition of Host Cells
37) The second step in viral replication, “entry”, is prevented by some antiviral drugs.
Answer: True
Difficulty: Easy
Learning Objective: LO 8.2 Describe the processes by which enveloped or non-enveloped
viruses may enter a cell.
Section Reference: Sec 8.2 Viral Entry and Uncoating
Answer: True
Difficulty: Easy
Learning Objective: LO 8.3 Identify the seven classes of virus, explaining how the classification
system is based on their replication system.
Section Reference: Sec 8.3 Viral Replication Strategies
39) The single-stranded RNA of positive-sense RNA viruses can act directly as mRNA for
translation in the cytoplasm of the host cell.
Answer: True
Difficulty: Easy
Learning Objective: LO 8.3 Identify the seven classes of virus, explaining how the classification
system is based on their replication system.
Section Reference: Sec 8.3 Viral Replication Strategies
40) Translation of mRNA for the production of viral proteins always takes place in the
cytoplasm of eukaryotic cells.
Answer: True
Difficulty: Medium
Learning Objective: LO 8.3 Identify the seven classes of virus, explaining how the classification
system is based on their replication system.
Section Reference: Sec 8.3 Viral Replication Strategies
41) Most enveloped viruses exit the host cell through cell lysis.
Answer: False
Difficulty: Easy
Learning Objective: LO 8.4 Explain how new viral particles assemble within the infected host
cell, describing the different processes involved in the egress of these newly created viruses from
the cell.
Section Reference: Sec 8.4 Viral Assembly and Egress
42) A nucleoside analog is a short nucleotide sequence that is complementary to a viral promoter
sequence.
Answer: False
Difficulty: Easy
Learning Objective: LO 8.5 Identify several antiviral drugs and the virus-specific processes that
they target.
Section Reference: Sec 8.5 Antiviral Agents
43) Host __________ is determined through the specific binding of the viral attachment protein
to the host cell receptor.
Difficulty: Easy
Learning Objective: LO 8.1 Explain how viruses recognize and attach to host cells, and how this
system determines the host range.
Section Reference: Sec 8.1 Recognition of Host Cells
44) Antibodies produced in response to a viral infection may specifically bind to the virus
particle to effectively block _______________ to the host cell.
Answer: attachment
Difficulty: Easy
Learning Objective: LO 8.1 Explain how viruses recognize and attach to host cells, and how this
system determines the host range.
Section Reference: Sec 8.1 Recognition of Host Cells
45) _________ __________ _________ is initiated by the binding of a virus to a host cell
receptor for the entry of the virus into the host cell via an endosome.
Difficulty: Easy
Learning Objective: LO 8.2 Describe the processes by which enveloped or non-enveloped
viruses may enter a cell.
Section Reference: Sec 8.2 Viral Entry and Uncoating
46) A viral fusion peptide contains a short hydrophobic amino acid sequence that helps facilitate
membrane fusion of the viral envelope to the cell membrane for entry into the host cell. The
protein _____________ functions as a fusion peptide for HIV entry into the host cell.
Answer: gp41
Difficulty: Medium
Learning Objective: LO 8.2 Describe the processes by which enveloped or non-enveloped
viruses may enter a cell.
Section Reference: Sec 8.2 Viral Entry and Uncoating
47) A bacterial cell that contains the integrated genome of a temperate bacteriophage is called a
______.
Answer: lysogen
Difficulty: Easy
Learning Objective: LO 8.3 Identify the seven classes of virus, explaining how the classification
system is based on their replication system.
Section Reference: Sec 8.3 Viral Replication Strategies
48) Most enveloped viruses exit their host cell through a process called __________.
Answer: budding
Difficulty: Easy
Learning Objective: LO 8.4 Explain how new viral particles assemble within the infected host
cell, describing the different processes involved in the egress of these newly created viruses from
the cell.
Section Reference: Sec 8.4 Viral Assembly and Egress
49. A chemical that is structurally similar to a normal nucleoside is called a nucleoside _______.
Answer: analog
Difficulty: Easy
Learning Objective: LO 8.5 Identify several antiviral drugs and the virus-specific processes that
they target.
Section Reference: Sec 8.5 Antiviral Agents
50) Several antiviral drugs that are produced today prevent attachment of the virus to the host
cell. What information do you need to know to design the drugs? Briefly describe possible
mechanisms of the drugs.
Answer:
Difficulty: Medium
Learning Objective: LO 8.1 Explain how viruses recognize and attach to host cells, and how this
system determines the host range.
Section Reference: Sec 8.1 Recognition of Host Cells
Solution: In order to design these drugs, scientists need to have a thorough knowledge of the
viral attachment protein and host cell receptor molecule and how these molecules interact with
one another. The antiviral drug would be designed to interfere with the attachment process either
by binding to the viral attachment protein or the host cell receptor molecule. The binding of the
drug to one of these two molecules will prevent them from interacting with one another and thus
prevent attachment.
51) The capsid for many mammalian viruses must be removed after it enters the cytoplasm. Why
is this important? Give an example of a virus where capsid removal occurs in the cell membrane.
Answer:
Difficulty: Easy
Learning Objective: LO 8.2 Describe the processes by which enveloped or non-enveloped
viruses may enter a cell.
Section Reference: Sec 8.2 Viral Entry and Uncoating
Solution: After the viral nucleocapsid enters the cytoplasm the capsid must be removed to expose
the viral nucleic acid. Viral nucleic acid exposure is required for nucleic acid replication and
transcription/translation of the viral genome. An example of a virus that uses this strategy is the
poliovirus.
52) Drugs that inhibit the acidification of the endosome block the replication of many viruses
that enter the cell through receptor-mediated endocytosis. Why are these drugs effective?
Answer:
Difficulty: Medium
Learning Objective: LO 8.2 Describe the processes by which enveloped or non-enveloped
viruses may enter a cell.
Section Reference: Sec 8.2 Viral Entry and Uncoating
Solution: Viruses that enter into the cell by receptor-mediated endocytosis need to escape from
the endosome. The acidification of the endosome causes a conformational change in some viral
capsid proteins. Some of these altered proteins function to aid in the release of the virus by
forming pores in the endosome membrane. This will facilitate the release of the capsid or the
viral nucleic acids. If the acidification did not occur, these pore-forming capsid proteins would
not assume the correct configuration for pore formation in the endosome membrane.
53) What are the functions of the retrovirus enzymes reverse transcriptase and integrase for the
replication of the virus?
Answer:
Difficulty: Medium
Learning Objective: LO 8.3 Identify the seven classes of virus, explaining how the classification
system is based on their replication system.
Section Reference: Sec 8.3. Viral replication strategies
Solution: The viral enzyme reverse transcriptase (RT) is an RNA-dependent DNA polymerase.
When the viral nucleic acid enters the cytoplasm, RT uses the single-stranded RNA as a template
and synthesizes a complementary DNA molecule. The enzyme also possesses RNase H activity
and it will degrade the RNA of the DNA/RNA heteroduplex and synthesize the complementary
DNA strand. Thus, RT forms a double-stranded DNA molecule from a single-stranded RNA
template. The DNA molecule enters into the nucleus and is integrated into the chromosome
using the viral integrase enzyme. Once the viral DNA is integrated into the chromosome it is
referred to as a prophage. The genes on the prophage can be transcribed into mRNA for
translation into viral proteins and the genome can be transcribed into genomic RNA using the
host cell DNA-dependent RNA polymerase II. The viral proteins and genome can assemble into
new virus particles.
54) Describe the series of events that usually occur for an enveloped virus to exit the cell with an
intact envelope containing the outer envelope viral proteins.
Answer:
Difficulty: Easy
Learning Objective: LO 8.4 Explain how new viral particles assemble within the infected host
cell, describing the different processes involved in the egress of these newly created viruses from
the cell.
Section Reference: Sec 8.4 Viral Assembly and Egress
Solution: All enveloped viruses acquire their envelope from a host cell membrane (usually the
plasma membrane). The membrane that makes up the envelope contains viral envelope proteins.
These proteins are first synthesized in the cell and a signal sequence will direct the protein for
insertion into the cell membrane. Next the assembled nucleocapsid must migrate to the area of
the membrane that contains the viral envelope proteins. The nucleocapsid buds through the
membrane in this area, acquiring its intact envelope.