General properties of
viruses
VIRUSES
Viruses are the smallest obligate intracellular
infective agents containing only one type of
nucleic acid (DNA or RNA) as their genome.
They do not possess a cellular organization
and lack the enzymes necessary for protein and
nucleic acid synthesis, They are resistant
differences to antibiotics.
I. MORPHOLOGY OF VIRUSES.
Size
Viruses are much smaller than other organisms.
The extracellular infectious virus particle is
called the virion. The size of viruses ranges
from 20 to 300 nm in diameter. The largest
virus is the smallpox virus (300 nm) and the
smallest is the parvovirus (20 nm)
Structure and Symmetry
1. STRUCTURE
The virion consists of a nucleic acid core
(genome) surrounded by a protein coat, the
capsid. The capsid together with the enclosed
nucleic acid is known as the nucleocapsid. The
capsid is composed of a c large number of
protein subunits (polypeptides) which are
known as capsomers. Certain viruses also
contain e envelope that surrounds the nucleic
acid. It is lipoprotein in nature.
SYMMETRY
Three types of symmetry are determined by the
arrangement of capsid around the nucleic acid
core.
(i) Icosahedral (cubical) symmetry
(ii) Helical symmetry
(iii) Complex symmetry
SHAPE
The overall shape of virus particles varies in
different groups . Pox virus is brick-shaped and
rabies virus is bullet shaped.
CHEMICAL PROPERTIES
NUCLEIC ACID
Viruses contain only one kind of nucleic acid,
either single or double stranded DNA or RNA.
VIRAL PROTEIN AND LIPIDS
Viruses contain protein which makes up the
capsid. In case of enveloped viruses, they
contain lipids (present in envelope).
CULTIVATION OF VIRUSES
As viruses multiply only in living cells, they
cannot be grown on any of the inanimate culture
medium. Three methods are employed for the
cultivation of viruses:
A. Animal inoculation.
B .Embryonated egg inoculation
C. Cell culture Parvovirus
• A. ANIMAL INOCULATION
Infant (suckling) mice are used in the isolation
of arboviruses and coxsackie viruses, many of
which do not grow in any other system. After
inoculation, animals are observed for signs of
disease or death. Later on, they are sacrificed
and tissues are tested for the presence of virus.
B. Embryonated Egg
Inoculation
• Embryonated hen's eggs
(7 to 12 days old) are
inoculated by one of the
several routes such as
amniotic sac yolk sac
and allantoic cavity
C. CELL CULTURE/TISSUE CULTURE
This is the type of culture routinely employed
for diagnostic virology. Cell cultures are
classified into three different types
(i) Primary cell culture
(ii) Diploid cell strains
(iii)Continuous cell lines
• (i) Primary cell cultures
These are normal cells freshly taken from the organs of
animal or human being and cultured. They are
capable of very limited growth in culture, perhaps 5-
10 divisions at the most.
(ii) Diploid cell strains
They can be subcultured for a limited number. After
about 50 serial subcultures they undergo senescence'
and the cell strain is lost.
(iii) Continuous cell lines
These are cells of a single type that are capable
of indefinite growth in vitro. They are usually
derived from cancerous tissue. They can be
serially cultivated indefinitely, therefore, they
are termed continuous cell lines.
LABORATORY DIAGNOSIS
OFVIRAL INFECTIONS
• A. Direct demonstration of virus and its components
• B. Isolation of virus
• C. Detection of the specific antibodies
DIRECT DEMONSTRATION OF VIRUSAND ITS
COMPONENTS
1. Electron Microscopy
The detection of virus by electron microscopy (EM) is
being used increasingly especially for viruses that
are difficult to culture. Clinical applications of
electron microscopy include detection of rotavirus
and hepatitis
2. Fluorescent Microscopy
3. Light Microscopy
Inclusion bodies in tissue sections may be
detected by light microscopy. Demonstration
of inclusion bodies helps in diagnosis of some
viral infections.
4.Viral Antigens
These may be detected by enzyme linked
immunosorbent assay (ELISA) and latex
agglutination.
5. Polymerase Chain Reaction (PCR)
With a PCR technique, a target DNA sequence can
be amplified to the point where it can readily be
identified using labelled probes in a hybridisation
assay. Thus viral DNA extracted from a very small
number of virions or infected cells can be detected.
The technique can be used for the diagnosis of
infections caused by HIV-1, HIV-2, hepatitis B
virus, and Epstein-Barr virus.
• C. DETECTION OF SPECIFIC
ANTIBODIES
The demonstration of a rise in titre of antiviral
antibodies during the course of a disease is
strong evidence that it is the aetiological agent.
For this, paired sera should be collected from
the patient, the acute sample collected early in
the course of the disease and the convalescent
sample collected ten to fourteen days later.
Examination of a single sample of serum is
meaningful when IgM specific antibodies are
detected.
CLASSIFICATION OF VIRUSES
• Viruses are classified on the basis of physical
and chemical biological, properties. Viruses
are broadly classified into DNA and RNA
viruses
PRIONS
Prions are infectious proteins without any
detectable nucleic acid. They are highly
resistant to physical and chemical agents. They
are resistant to heat (90°C for three minutes),
UV rays and nucleases and sensitive to
proteases. They produce slow infections with
long incubation period (in years).

Presentation virology.pptx

  • 1.
  • 2.
    VIRUSES Viruses are thesmallest obligate intracellular infective agents containing only one type of nucleic acid (DNA or RNA) as their genome. They do not possess a cellular organization and lack the enzymes necessary for protein and nucleic acid synthesis, They are resistant differences to antibiotics.
  • 3.
    I. MORPHOLOGY OFVIRUSES. Size Viruses are much smaller than other organisms. The extracellular infectious virus particle is called the virion. The size of viruses ranges from 20 to 300 nm in diameter. The largest virus is the smallpox virus (300 nm) and the smallest is the parvovirus (20 nm)
  • 5.
    Structure and Symmetry 1.STRUCTURE The virion consists of a nucleic acid core (genome) surrounded by a protein coat, the capsid. The capsid together with the enclosed nucleic acid is known as the nucleocapsid. The capsid is composed of a c large number of protein subunits (polypeptides) which are known as capsomers. Certain viruses also contain e envelope that surrounds the nucleic acid. It is lipoprotein in nature.
  • 7.
    SYMMETRY Three types ofsymmetry are determined by the arrangement of capsid around the nucleic acid core. (i) Icosahedral (cubical) symmetry (ii) Helical symmetry (iii) Complex symmetry SHAPE The overall shape of virus particles varies in different groups . Pox virus is brick-shaped and rabies virus is bullet shaped.
  • 9.
    CHEMICAL PROPERTIES NUCLEIC ACID Virusescontain only one kind of nucleic acid, either single or double stranded DNA or RNA. VIRAL PROTEIN AND LIPIDS Viruses contain protein which makes up the capsid. In case of enveloped viruses, they contain lipids (present in envelope).
  • 10.
    CULTIVATION OF VIRUSES Asviruses multiply only in living cells, they cannot be grown on any of the inanimate culture medium. Three methods are employed for the cultivation of viruses: A. Animal inoculation. B .Embryonated egg inoculation C. Cell culture Parvovirus
  • 11.
    • A. ANIMALINOCULATION Infant (suckling) mice are used in the isolation of arboviruses and coxsackie viruses, many of which do not grow in any other system. After inoculation, animals are observed for signs of disease or death. Later on, they are sacrificed and tissues are tested for the presence of virus.
  • 13.
    B. Embryonated Egg Inoculation •Embryonated hen's eggs (7 to 12 days old) are inoculated by one of the several routes such as amniotic sac yolk sac and allantoic cavity
  • 14.
    C. CELL CULTURE/TISSUECULTURE This is the type of culture routinely employed for diagnostic virology. Cell cultures are classified into three different types (i) Primary cell culture (ii) Diploid cell strains (iii)Continuous cell lines
  • 16.
    • (i) Primarycell cultures These are normal cells freshly taken from the organs of animal or human being and cultured. They are capable of very limited growth in culture, perhaps 5- 10 divisions at the most. (ii) Diploid cell strains They can be subcultured for a limited number. After about 50 serial subcultures they undergo senescence' and the cell strain is lost.
  • 17.
    (iii) Continuous celllines These are cells of a single type that are capable of indefinite growth in vitro. They are usually derived from cancerous tissue. They can be serially cultivated indefinitely, therefore, they are termed continuous cell lines.
  • 18.
    LABORATORY DIAGNOSIS OFVIRAL INFECTIONS •A. Direct demonstration of virus and its components • B. Isolation of virus • C. Detection of the specific antibodies DIRECT DEMONSTRATION OF VIRUSAND ITS COMPONENTS 1. Electron Microscopy The detection of virus by electron microscopy (EM) is being used increasingly especially for viruses that are difficult to culture. Clinical applications of electron microscopy include detection of rotavirus and hepatitis
  • 19.
    2. Fluorescent Microscopy 3.Light Microscopy Inclusion bodies in tissue sections may be detected by light microscopy. Demonstration of inclusion bodies helps in diagnosis of some viral infections.
  • 20.
    4.Viral Antigens These maybe detected by enzyme linked immunosorbent assay (ELISA) and latex agglutination.
  • 21.
    5. Polymerase ChainReaction (PCR) With a PCR technique, a target DNA sequence can be amplified to the point where it can readily be identified using labelled probes in a hybridisation assay. Thus viral DNA extracted from a very small number of virions or infected cells can be detected. The technique can be used for the diagnosis of infections caused by HIV-1, HIV-2, hepatitis B virus, and Epstein-Barr virus.
  • 22.
    • C. DETECTIONOF SPECIFIC ANTIBODIES The demonstration of a rise in titre of antiviral antibodies during the course of a disease is strong evidence that it is the aetiological agent. For this, paired sera should be collected from the patient, the acute sample collected early in the course of the disease and the convalescent sample collected ten to fourteen days later. Examination of a single sample of serum is meaningful when IgM specific antibodies are detected.
  • 23.
    CLASSIFICATION OF VIRUSES •Viruses are classified on the basis of physical and chemical biological, properties. Viruses are broadly classified into DNA and RNA viruses
  • 24.
    PRIONS Prions are infectiousproteins without any detectable nucleic acid. They are highly resistant to physical and chemical agents. They are resistant to heat (90°C for three minutes), UV rays and nucleases and sensitive to proteases. They produce slow infections with long incubation period (in years).