Microbiology and Immunology

(Axel Boer) #1
WORLD OF MICROBIOLOGY AND IMMUNOLOGY Virus replication

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manufacture the RNA that is eventually packaged into the new
virus particles. The main example is the Retroviruses(the
Human ImmunodeficiencyViruses belong here). Finally, a
group of viruses consist of double-stranded DNA that is used
to produce a RNA intermediate. An example is the
Hepadnaviruses.
An aspect of virology is the identification of viruses.
Often, the diagnosis of a viral illness relies, at least initially, on
the visual detection of the virus. For this analysis, samples are
prepared for electron microscopy using a technique called
negative staining, which highlights surface detail of the virus
particles. For this analysis, the shape of the virus is an impor-
tant feature.
A particular virus will have a particular shape. For
example, viruses that specifically infect bacteria, the so-called
bacteriophages, look similar to the Apollo lunar landing space-
craft. A head region containing the nucleic acid is supported
on a number of spider-like legs. Upon encountering a suitable
bacterial surface, the virus acts like a syringe, to introduce the
nucleic acid into the cytoplasm of the bacterium.
Other viruses have different shapes. These include
spheres, ovals, worm-like forms, and even irregular (pleomor-
phic) arrangements. Some viruses, such as the influenzavirus,
have projections sticking out from the surface of the virus.
These are crucial to the infectious process.
As new species of eukaryotic and prokaryotic organ-
isms are discovered, no doubt the list of viral species will con-
tinue to grow.

See alsoViral genetics; Virus replication

VIRULENCE•seeMICROBIOLOGY, CLINICAL

VVirus replicationIRUS REPLICATION

Viral replication refers to the means by which virus particles
make new copies of themselves.
Virusescannot replicate by themselves. They require
the participation of the replication equipment of the host cell
that they infect in order to replicate. The molecular means by
which this replication takes place varies, depending upon the
type of virus.
Viral replication can be divided up into three phases:
initiation, replication, and release.
The initiation phase occurs when the virus particle
attaches to the surface of the host cell, penetrates into the cell
and undergoes a process known as uncoating, where the viral
genetic material is released from the virus into the host cell’s
cytoplasm. The attachment typically involves the recognition
of some host surface molecules by a corresponding molecule
on the surface of the virus. These two molecules can associate
tightly with one another, binding the virus particle to the sur-
face. A well-studied example is the haemagglutinin receptor of
the influenzae virus. The receptors of many other viruses have
also been characterized.

A virus particle may have more than one receptor mol-
ecule, to permit the recognition of different host molecules, or
of different regions of a single host molecule. The molecules
on the host surface that are recognized tend to be those that are
known as glycoproteins. For example, the human immunode-
ficiency virusrecognizes a host glycoprotein called CD4.
Cells lacking CD4 cannot, for example, bind the HIVparticle.
Penetration of the bound virus into the host interior
requires energy. Accordingly, penetration is an active step, not
a passive process. The penetration process can occur by sev-
eral means. For some viruses, the entire particle is engulfed by
a membrane-enclosed bag produced by the host (a vesicle) and
is drawn into the cell. This process is called endocytosis. Polio
virus and orthomyxovirus enters a cell via this route. A second
method of penetration involves the fusion of the viral mem-
brane with the host membrane. Then the viral contents are
directly released into the host. HIV, paramyxoviruses, and her-
pesviruses use this route. Finally, but more rarely, a virus par-
ticle can be transported across the host membrane. For
example, poliovirus can cause the formation of a pore through
the host membrane. The viral DNAis then released into the
pore and passes across to the inside of the host cell.
Once inside the host, the viruses that have entered via
endocytosis or transport across the host membrane need to
release their genetic material. With poxvirus, viral proteins
made after the entry of the virus into the host are needed for
uncoating. Other viruses, such as adenoviruses, her-
pesviruses, and papovaviruses associate with the host mem-
brane that surrounds the nucleusprior to uncoating. They are
guided to the nuclear membrane by the presence of so-called
nuclear localization signals, which are highly charged viral
proteins. The viral genetic material then enters the nucleus via
pores in the membrane. The precise molecular details of this
process remains unclear for many viruses.
For animal viruses, the uncoating phase is also referred
to as the eclipse phase. No infectious virus particles can be
detected during that 10–12 hour period of time.
In the replication, or synthetic, phase the viral genetic
material is converted to deoxyribonucleic acid(DNA), if the
material originally present in the viral particle is ribonucleic
acid(RNA). This so-called reverse transcriptionprocess needs
to occur in retroviruses, such as HIV. The DNA is imported
into the host nucleus where the production of new DNA,
RNA, and protein can occur. The replication phase varies
greatly from virus type to virus type. However, in general, pro-
teins are manufactured to ensure that the cell’s replication
machinery is harnessed to permit replication of the viral
genetic material, to ensure that this replication of the genetic
material does indeed occur, and to ensure that this newly made
material is properly packaged into new virus particles.
Replication of the viral material can be a complicated
process, with different stretches of the genetic material being
transcribed simultaneously, with some of these geneproducts
required for the transcription of other viral genes. Also repli-
cation can occur along a straight stretch of DNA, or when the
DNA is circular (the so-called “rolling circle” form). RNA-
containing viruses must also undergo a reverse transcription

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