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Viruses, Viroids, and Prions
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contagium vivum fluidum
a contagious fluid.
virus
are alive when they multiply in the host cells they infect
Contain a single type of nucleic acid, either DNA or RNA.
Contain a protein coat that surrounds the nucleic acid.
Cause the synthesis of specialized structures that can transfer the viral nucleic acid to other cells.
Viroids
RNA only
Virusoids
RNA with protein coat
Satellites
– nucleic acid only
prions
protein only
Wendell Stanley
an American chemist, isolated tobacco mosaic virus, making it possible for the first time to carry out chemical and structural studies on a purified virus
Dmitri Ivanowski
in 1892, he showed that tobacco mosaic disease (TMD) was transmitted via plant extracts
obligatory intracellular parasites
viruses are —, they absolutely require living host cells in order to multiply.
host range
is the spectrum of host cells the virus can infect.
host tropism
most viruses are able to infect specific types of cells of only one host species
bacteriophages, or phages.
Viruses that infect bacteria
virus’s requirements for its specific attachment to the host cell and the availability within the potential host of cellular factors required for viral multiplication
The particular host range of a virus is determined by the
the outer surface of the virus must chemically interact with specific receptor sites on the surface of the cell
For the virus to infect the host cell,
phage therapy
using bacteriophages to treat bacterial infections
20 to 1000 nm
size of viruses
virion
is a complete, fully developed, infectious viral particle composed of nucleic acid and surrounded by a protein coat outside a host cell.
nucleic acids and differences in the structures of their coats
Viruses are classified by their
true
t or f. viral genes are encoded by either DNA or RNA— but never both.
capsid
The nucleic acid of a virus is protected by a protein coat called
capsomeres
Each capsid is composed of protein subunits
envelope
covers viruses, which usually consists of some combination of lipids, proteins, and carbohydrates
spikes
which are carbohydrate-protein complexes that project from the surface of the envelope
hemagglutination
resulting clumping in influenza virus
nonenveloped viruses
Viruses whose capsids aren’t covered by an envelope
regions of the genes that code for these viruses’ surface proteins are susceptible to mutations
how can some viruses escape antibodies?
electron microscopy and a technique called X-ray crystallography.
The structure of these capsids has been revealed by
helical virus, polyhedral virus, enveloped virus, complex virus
different morphology of viruses
Helical Viruses
resemble long rods that may be rigid or flexible.
The viral nucleic acid is found within a hollow, cylindrical capsid that has a helical structure
Rabies and ebola
Polyhedral Viruses
capsid is in the icosahedron, a regular polyhedron with 20 triangular faces and 12 corners
ex. adenovirus
Enveloped Viruses
are roughly spherical
ex. influenza virus
enveloped helical or enveloped polyhedral viruses
When helical or polyhedral viruses are enclosed by envelopes, they are called —
Complex Viruses
viruses that have complicated structures
bacteriophage
viral species
is a group of viruses sharing the same genetic information and ecological niche (host range)
are designated by descriptive common names, such as human immunodeficiency virus (HIV), with subspecies (if any) designated by a number (HIV-1).
• International Committee on Taxonomy of Viruses (ICTV)
classify viruses based on host range, virion morphology, and genome type
suspensions of bacteria in liquid media or in bacterial cultures on solid media
Bacteriophages can be grown either in
plaque method
A bacteriophage sample is mixed with host bacteria and melted agar. The agar containing the bacteriophages and host bacteria is then poured into a Petri plate containing a hardened layer of agar growth medium. The virus-bacteria mixture solidifies into a thin top layer that contains a layer of bacteria approximately one cell thick.
plaque
number of clearings, visible against a lawn of bacterial growth on the surface of the agar
plaque-forming units (PFU)
the concentrations of viral suspensions measured by the number of plaques are usually expressed in terms of
living animals, embryonated eggs, or cell cultures
three methods are commonly used for culturing animal viruses.
Animal inoculation
may be used as a diagnostic procedure for identifying and isolating a virus from a clinical specimen.
embryonated egg inoculation
A hole is drilled in the shell of the embryonated egg, and a viral suspension or suspected virus-containing tissue is injected into the egg’s fluid.
by embryo cell damage, or by the formation of typical pocks or lesions on the egg membranes
how is viral growth signaled in an embryonated eggs
cell cultures
have replaced embryonated eggs as the preferred type of growth medium for many viruses.
cell culture lines
are started by treating a slice of animal tissue with enzymes that separate the individual cells
western blotting and cytopathic effects
methods of viral identification
cytopathic effect (CPE)
cell deterioration, can be detected and counted in much the same way as plaques caused by bacteriophages on a lawn of bacteria and reported as PFU/ml.
primary or continuous cell lines
Viruses may be grown in
Primary cell lines
derived from tissue slices, tend to die out after only a few generations.
diploid cell lines
cell lines developed from human embryos can be maintained for about 100 generations and are widely used for culturing viruses that require a human host.
continuous cell lines
cell lines used when viruses are routinely grown in a laboratory
These are transformed (cancerous) cells that can be maintained through an indefinite number of generations, and they’re sometimes called immortal cell lines
Western blotting
most commonly used means of viral identification.
, the virus is detected and identified by its reaction with antibodies
restriction fragment length polymorphisms (RFLPs) and the polymerase chain reaction (PCR)
modern molecular methods of identifying viruses
Viral enzymes
are almost entirely concerned with replicating or processing viral nucleic acid.
host cell enzymes
are used for energy production, synthesizing viral proteins, synthesizing viral nucleic acids
it must invade a host cell and take over the host’s metabolic machinery
how do viruses multiply
one-step growth curve
demonstrates multiplication of viruses
The data are obtained by infecting every cell in a culture and then testing the culture medium and cells for virions and viral proteins and nucleic acids.
the lytic cycle or the lysogenic cycle
Bacteriophages can multiply by two alternative mechanisms:
lytic cycle
ends with the lysis and death of the host cell
lysogenic cycle
host cell remains alive
Virulent bacteriophages
always cause the lytic cycle, which ends with the destruction of the bacterial cell
Temperate bacteriophages
lysogenic phages do not immediately initiate the lytic cycle, but rather, their DNA remains integrated into bacterial cell chromosome, generation after generation
T-even bacteriophages
example of the lytic cycle.
The length of DNA contained in these bacteriophages is only about 6% of that contained in E. coli, yet the phage has enough DNA for over 100 genes.
attachment, penetration, biosynthesis, maturation, and release
multiplication cycle of these phages occurs in five stages
Attachment
an attachment site on the virus attaches to a complementary receptor site on the bacterial cell.
Penetration
Phage penetrates host cell and injects its DNA
Biosynthesis
Phage DNA directs synthesis of viral components by the host cells
Maturation
Viral components are assembled into virions
Release
Host cell lyses, and new virions are released
The lysogenic cells are immune to reinfection by the same phage.
The host cell may exhibit new properties (phage conversion), e.g. produces toxin encoded by a prophage gene
It makes specialized transduction possible.
Three Important Results of Lysogeny
Specialized transduction
when a prophage is excised from its host chromosome, it can take with it a bit of the adjacent DNA from the bacterial chromosome
a virus needs live host cells but must stop synthesis of host proteins, so the viral genes are translated
early proteins translated from the viral genome may block transcription, existing mRNA, or inprogress translation
Multiplication of Animal Viruses
attachment, entry, uncoating, biosynthesis, maturation, and release
6 stages of Multiplication of Animal Viruses
receptor-mediated endocytosis
fusion of the viral envelope and cell membrane
2 mechanisms of the entry of animal viruses into host cells.
Adenoviridae
Poxviridae
Herpesviridae
Papovaviridae
Hepadnaviridae
The Biosynthesis of DNA Viruses
Piconaviridae
Togaviridae
Rhabdoviridae
Reoviridae
The Biosynthesis of RNA Viruses
Retroviridae
The Biosynthesis of RNA Viruses that Use DNA
Parvoviridae
DNA, single-stranded
Herpesviridae Papovaviridae Poxviridae
DNA, double-stranded
Hepadnaviridae
DNA, reverse transcriptase
Picornaviridae Togaviridae
RNA, + strand
Rhabdoviridae
RNA, - strand
Reoviridae
RNA, double-stranded
Retroviridae
RNA, reverse transcriptase
Influenza virus
is one of the few RNA viruses that replicates in the nucleus of cells.
viral glycoproteins; engulfed; budding
In influenza virus infection, — attach the virus to a host epithelial cell. As a result, the virus is —. Viral RNA and viral proteins are made and assembled into new virions that are released by —.
oncogenes
can be activated to abnormal functioning by a variety of agents, including viruses
genetic material
— of oncogenic viruses integrates into the host cell’s DNA and replicates along with the host cell’s chromosome
transformation
tumor cells undergo
tumor-specific transplantation antigen (TSTA)
many tumor cells contain— on their cell surface
human papillomavirus (HPV)
virtually all cervical and anal cancers are caused by
Epstein-Barr virus (EBV)
was isolated from Burkitt’s lymphoma cells in 1964 by Michael Epstein & Yvonne Barr
hepatitis B virus (HBV)
caused liver cancer
human papillomavirus (HPV), Epstein-Barr virus (EBV), hepatitis B virus (HBV)
example of DNA Oncogenic Viruses
sarcoma viruses, mammary tumor viruses, feline leukemia virus (FeLV)
example of RNA Oncogenic Viruses
reverse transcriptase
the ability of retroviruses to induce tumors is related to their production of a —, the provirus becomes integrated into the host cell’s DNA
promoters
turn on oncogenes or other cancercausing factors
tumors
in the early 1900s,—were regressed in patients with concurrent viral infections
antitumor activity
in the 1920s, experimentally-induced viral infections in cancer patients suggested
oncolytic viruses
selectively infect and kill tumor cells or cause an immune response against tumor cells