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General Characteristics of Viruses
• Obligate intracellular, unable to self-replicate.
• Once inside living cells, viruses induce the host cell to synthesize virus
particles.
• The genome is either DNA or RNA (single or double stranded).
• Viruses do not have a system to produce ATP.
• Viruses range in size from 25 to 270 nm.
• Viral tropism!!
• The classification of viruses is based on nucleic acid type, size and shape of
virion, and presence or absence of an envelope.
• Viral Structure
• I . Virion is the entire viral particle.
• 2. Capsid is the protein coat that encloses the genetic material.
• 3. Capsomer is the protein subunit that makes up the capsid.
• 4. Nucleocapsid is composed of the capsid and genetic material.
• 5. The envelope is the outer coating composed of a phospholipid bilayer, which
is composed of viral-encoded glycoproteins and sometimes viral encoded
matrix proteins. The envelope is derived from a host cell's membrane.
• Some viruses use the plasma membrane, whereas others use endoplasmic
reticulum, Golgi, or nuclear membranes. Naked nucleocapsids are viruses
with no envelopes.
Replication
• l. Adsorption is attachment of the virus to a specific
receptor on the host cell.
• 2. Penetration is entry of the virus into the host cell.
• 3. Uncoating occurs when there is either the
separation of the capsid from the genome or
rearrangement of the capsid proteins exposing the
genome for transcription and replication.
• 4. The eclipse period is the stage when the genetic
material is replicated but intact virions are not yet
detectable.
• 5. Assembly (maturation): Genetic material is
assembled into a protein coat.
• 6. Viruses are then released from the host cell.
• a. Cell lysis: Naked viruses lyse host cell and
leave through a hole in the plasma membrane.
• b. Budding: Intact virion pushes outward from a
host's membrane (exocytosis). The membrane
wraps around the virion; the membrane is
cleaved and then resealed around the virion,
thus becoming the viral envelope.
Lab diagnosis
Specimen Processing for Diagnosing Viral Diseases
• Samples for viral culture must be placed into a viral transport medium (VTM).
• VTM contains:
• a. Buffered saline
• b. Protein stabilizers
• c. Antimicrobials that inhibit bacterial and fungal growth
• Ideally all specimens collected for detection of virus should be processed immediately
• Specimens for viral isolation should not be allowed to sit at room or higher
temperature.
• Specimens should be kept cool (4°C) and immediately transported to the laboratory.
Delay of more than 24 hours, freeze at -70°C (not -20°C).
• For storage up to 5 days, specimens are held at 4°C. Storage for 6 days or longer
should be at (preferably) –70°C.
VIRAL IDENTIFICATION methods
• A. Histology and Cytology
• Cellular inclusions are diagnostic for many viruses.
• Because most DNA viruses replicate in the nucleus, they often produce nuclear
inclusions. However, some DNA viruses are assembled elsewhere in the cell.
• RNA viruses produce cytoplasmic inclusions (assembled in the cytoplasm).
• HSV and VZV cause intranuclear inclusions. CMV induces enlarged (cytomegalic) cells
with a basophilic intranuclear inclusion referred to as "owl eye" inclusion.
• B. Viral Isolation:
• 1. Cell culture
• A. Cell culture is an important means of diagnosing viral infections. Cell cultures
require nutritionally rich complex media.
• The media often contain fecal calf serum as a nutrient.
• Clinical specimens are processed and added to the cell cultures.
• Viruses have an affinity for specific cell types (e.g, respiratory epithelium, neurons,
etc.).
• Propagation of viruses is therefore dependent upon providing suitable host cells.
• Some viruses have not yet been grown in vitro.
• B. Slides are made from infected cell cultures and examined for cellular changes,
including clumping, vacuoles, inclusions, granules, cell fusion (i.e., syncytium-
multinucleated cell development), and cellular destruction. These visible changes are
referred to as cytopathic effect (CPE). However, many viruses replicate without
producing CPE.
• 2. Embryonated eggs are sometimes used for growth of viruses. Eggs are not typically used
for diagnosis of viral infection but to cultivate viruses for research studies and vaccine
preparation, as in the case of influenza virus.
• 3. Animal models are sometimes used in research studies.
• C. Electron Microscopy
• Most individual virions can only be seen by electron microscopy.
• Poxviruses are about the size of some small bacteria & can be seen by light microscope.
• Electron microscopy is sometimes used to identify Norwalk viruses, astrovirus,
calicivirus, and coronavirus. Electron microscopy is expensive, requires expertise, and is
usually not very sensitive. For these reasons, electron microscopy is not commonly used.
• D. Other Methods for Identification
• 1. Detection of host antibodies directed against specific viruses
• 2. Direct detection of viral antigens in clinical specimens
• 3. Viral gene probes and nucleic acid amplification.
Alyazeed Hussein, BSc, SUST
This has been a presentation of Alyazeed Hussein
Thanks for your attention and kind patience
@elyazeed7
@Alyazeed7ussein

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General Characteristics of Viruses

  • 1. General Characteristics of Viruses • Obligate intracellular, unable to self-replicate. • Once inside living cells, viruses induce the host cell to synthesize virus particles. • The genome is either DNA or RNA (single or double stranded). • Viruses do not have a system to produce ATP. • Viruses range in size from 25 to 270 nm. • Viral tropism!! • The classification of viruses is based on nucleic acid type, size and shape of virion, and presence or absence of an envelope. • Viral Structure • I . Virion is the entire viral particle. • 2. Capsid is the protein coat that encloses the genetic material. • 3. Capsomer is the protein subunit that makes up the capsid. • 4. Nucleocapsid is composed of the capsid and genetic material. • 5. The envelope is the outer coating composed of a phospholipid bilayer, which is composed of viral-encoded glycoproteins and sometimes viral encoded matrix proteins. The envelope is derived from a host cell's membrane. • Some viruses use the plasma membrane, whereas others use endoplasmic reticulum, Golgi, or nuclear membranes. Naked nucleocapsids are viruses with no envelopes.
  • 2.
  • 3.
  • 4.
  • 5.
  • 6. Replication • l. Adsorption is attachment of the virus to a specific receptor on the host cell. • 2. Penetration is entry of the virus into the host cell. • 3. Uncoating occurs when there is either the separation of the capsid from the genome or rearrangement of the capsid proteins exposing the genome for transcription and replication. • 4. The eclipse period is the stage when the genetic material is replicated but intact virions are not yet detectable. • 5. Assembly (maturation): Genetic material is assembled into a protein coat. • 6. Viruses are then released from the host cell. • a. Cell lysis: Naked viruses lyse host cell and leave through a hole in the plasma membrane. • b. Budding: Intact virion pushes outward from a host's membrane (exocytosis). The membrane wraps around the virion; the membrane is cleaved and then resealed around the virion, thus becoming the viral envelope.
  • 7.
  • 8.
  • 9.
  • 10.
  • 11.
  • 13. Specimen Processing for Diagnosing Viral Diseases • Samples for viral culture must be placed into a viral transport medium (VTM). • VTM contains: • a. Buffered saline • b. Protein stabilizers • c. Antimicrobials that inhibit bacterial and fungal growth • Ideally all specimens collected for detection of virus should be processed immediately • Specimens for viral isolation should not be allowed to sit at room or higher temperature. • Specimens should be kept cool (4°C) and immediately transported to the laboratory. Delay of more than 24 hours, freeze at -70°C (not -20°C). • For storage up to 5 days, specimens are held at 4°C. Storage for 6 days or longer should be at (preferably) –70°C.
  • 14.
  • 15. VIRAL IDENTIFICATION methods • A. Histology and Cytology • Cellular inclusions are diagnostic for many viruses. • Because most DNA viruses replicate in the nucleus, they often produce nuclear inclusions. However, some DNA viruses are assembled elsewhere in the cell. • RNA viruses produce cytoplasmic inclusions (assembled in the cytoplasm). • HSV and VZV cause intranuclear inclusions. CMV induces enlarged (cytomegalic) cells with a basophilic intranuclear inclusion referred to as "owl eye" inclusion. • B. Viral Isolation: • 1. Cell culture • A. Cell culture is an important means of diagnosing viral infections. Cell cultures require nutritionally rich complex media. • The media often contain fecal calf serum as a nutrient. • Clinical specimens are processed and added to the cell cultures. • Viruses have an affinity for specific cell types (e.g, respiratory epithelium, neurons, etc.). • Propagation of viruses is therefore dependent upon providing suitable host cells. • Some viruses have not yet been grown in vitro.
  • 16. • B. Slides are made from infected cell cultures and examined for cellular changes, including clumping, vacuoles, inclusions, granules, cell fusion (i.e., syncytium- multinucleated cell development), and cellular destruction. These visible changes are referred to as cytopathic effect (CPE). However, many viruses replicate without producing CPE. • 2. Embryonated eggs are sometimes used for growth of viruses. Eggs are not typically used for diagnosis of viral infection but to cultivate viruses for research studies and vaccine preparation, as in the case of influenza virus. • 3. Animal models are sometimes used in research studies. • C. Electron Microscopy • Most individual virions can only be seen by electron microscopy. • Poxviruses are about the size of some small bacteria & can be seen by light microscope. • Electron microscopy is sometimes used to identify Norwalk viruses, astrovirus, calicivirus, and coronavirus. Electron microscopy is expensive, requires expertise, and is usually not very sensitive. For these reasons, electron microscopy is not commonly used. • D. Other Methods for Identification • 1. Detection of host antibodies directed against specific viruses • 2. Direct detection of viral antigens in clinical specimens • 3. Viral gene probes and nucleic acid amplification.
  • 17.
  • 18. Alyazeed Hussein, BSc, SUST This has been a presentation of Alyazeed Hussein Thanks for your attention and kind patience @elyazeed7 @Alyazeed7ussein