3. BeijerinckBeijerinck
19211921
Virus (Latin- poison and
other noxious substances,
first used in English in 1392)
"Organisms at the edge of
life”
At the twilight zone
separating the “living” from
the “nonliving”.
Living chemicals ????
Introduction
4.
5. Introduction
VirusesViruses - Obligate intracellular infectious agents
(20-400 nm in diameter) containing only one kind
of nucleic acid (DNA or RNA as their genome)
1000 nm = 1 µm
Morphological definitions:
Capsid- Protein shell or coat that encloses the
nucleic acid genome
Capsomers- Morphologic units composing the
capsid; Shapes - vary (spherical/wedge)
6.
7. Envelope- A lipid containing membrane that
surrounds some virus particles and are acquired
during viral maturation by a budding process
through a cellular membrane of host cell
Peplomers- Virus encoded glycoprotein exposed
on the surface of the envelope (also known as
spikes)
Nucleocapsid- Capsid together with the
enclosed N/A
8. VirionVirion – Complete virus particle
Herpes, Orthomyxo viruses Nucleocapsid + Envelope
Papova viruses, Picorna viruses Nucleocapsid
Intactness of structure and the property of
infectiousness
9. Origin of viruses
Regressive hypothesis (degeneracy
hypothesis)
Viruses are remnants of cellular organisms.
Progressive hypothesis or Cellular
origin hypothesis (vagrancy
hypothesis)
Some viruses may have evolved from bits of DNA / RNA that
"escaped" from the genes (plasmids or transposons) of a larger
organism.
Coevolution hypothesis (virus-first
hypothesis)
Viruses may have evolved from complex molecules of protein and
nucleic acid at the same time as cells first appeared on earth.
13. NUCLEIC ACID CORE (GENOME):
StructureStructure: contains either DNA or RNA
SizeSize: 3-3000 kbp
StrandednessStrandedness: either single-stranded (RNA viruses
except Reo-) or double-stranded (DNA viruses
except Parvo-)
SegmentationSegmentation: NA as single or several segments
(Influenza virus has 8 RNA molecules, each
carrying different genetic information. Such viruses
are termed segmented viruses)
14. VIRAL CAPSID:
COMPOSITION
CapsomersCapsomers: morphological subunits
FUNCTIONS
Protection from physical, chemical and
enzymatic damage
Recognition of the host cell- (Viral attachment
protein-VAP and cellular receptor)
16. ENVELOPE:
Lipid bilayer (derived from host cell membrane) and
virus-coded gp (peplomers) as spikes
Matrix proteins: internal virion proteins that links the
internal nucleocapsid
Glycoproteins: Transmembrane proteins, anchored to
the membrane; also includes transport channels (ion-
channels)
Influenza virus- Hemagglutinin and Neuraminidase
17. ENVELOPE FUNCTIONS
Promote interaction with nucleocapsid proteins (final
stage of assembly)
Act as VAPs to cellular receptors
Major viral antigens
Interaction (spikes) with neutralizing antibodies
Tegument: Herpesvirus nucleocapsid are enveloped but
have a featureless layer of tegument interposed
between the nucleocapsid and envelope.
Function ????
18. VIRAL PROTEINS:
Structural proteinsStructural proteins: essential for the formation
of new viral particles.
Some are associated with NA
Some form protective layers (capsid and envelope)
VAP
Antigenicity
EnzymesEnzymes: essential for initiation of replication
Polymerases, Proteases, Endonucleases
19.
20. Chemical Properties - Resistance
Temperature:
Enveloped viruses are more heat-labile
Inactivated at 560
C-30’ (exception- HBV) and few sec at 1000
C.
Some may be preserved by lyophilization
Salts:
1 M salt solution e.g., MgCl2, MgSO4
pH:
Usu. stable between pH 5 and 9
Enteroviruses – resistant to acidic conditions
21. Radiation: UV and ionising radiation inactivates viruses
Photodynamic Inactivation
Vital dyes- Toluidene blue; Visible light - Inactivation
Disinfectants
Most viruses are destroyed by oxidising agents such as
chlorine, iodine and hydrogen peroxide. However, majority of
viruses are resistant to phenol; chlorination does not always
inactivate enteroviruses or hepatitis viruses, particularly if
present with organic or faecal material.
22. Viral hemagglutination
Hirst (1941)
When viral particles are added to a red cell suspension, the
virus particles are adsorbed to each red cell, bridge
between them and bind them together forming a lattice
Hemagglutinin + N-acetyl neuraminic acid
(VIRUS + RBC)
Agglutination occurs rapidly at 0o
C
Eluted at 37o
C
About 107
influenza virions are needed to cause
hemagglutination visible to the naked eye.
23.
24. Neuraminidase (Receptor destroying enzyme)
Virus – No alteration
Destroy receptor on RBCs
Destruction of the surface receptors result in the reversal of
haemagglutination and the release of the virus from the
RBC cell surface.
Epithelial cells of the respiratory tract have the same
properties as those of RBCs so far as virus adsorption is
concerned.
Influenza virus normally remain confined to the respiratory
tract because the protease enzyme that cleave HA are
common only at those sites.