Viruses: Why Are We Learning About Them?
Viruses: Why Are We Learning About Them?
Hepatitis
HIV
Flu
Measles
Mumps
Viruses
Small
Subcellular agents
Unable to multiply
outside a host cell
Main purpose is to
deliver its genome into
the host cell to allow its
expression by the host
cell
Structure and Function
Inert outside the host
cell
Unable to generate
energy of their own
Depend on the
biochemical machinery
of eukaryotic or
prokaryotic cells for
replication
Structure and Function
Capsid
The capsid is the protein
shell that encloses the
nucleic acid
It protects the nucleic
acid from digestion by
enzymes
Contains special sites on
its surface that allow the
virion to attach to a host
cell
Structure and Function
Capsid
Provides proteins
that enable the virion
to penetrate the host
cell membrane and, in
some cases, to inject
the infectious nucleic
acid into the cell's
cytoplasm
Structure and Function
DNA/RNA
Long molecules which
carry genetic
information
Nucleic acid contains
genetic information
necessary to program
the synthetic machinery
of host cell for viral
replication
Structure and Function
Tail fibers
The virus has tails which
it attaches to the host
surface by means of
proteinaceous pins.
The tail contracts and the
tail plug penetrates the cell
wall and underlying
membrane, injecting the
viral nucleic acids into the
cell.
Viral populations do not
grow through cell division
Use host cell to produce
multiple copies and
assemble in the cell
Assembled virus, virion,
include one type of
nucleic acid (RNA/DNA)
and in simplest viruses,
has protective protein
coat
Assembly type of
replication is unique to
viruses
PRINCIPLE EVENTS
INVOLVED IN VIRAL
REPLICATION
1. ADSORPTION
2. PENETRATION
3. UNCOATING
5. ASSEMBLY/MATURATION
6. RELEASE
ADSORPTION
VIRUS ATTACHES TO THE CELL SURFACE VIA IONIC
INTERACTIONS WHICH ARE TEMPERATURE
INDEPENDENT
HOW?
VIRAL ATTACHMENT PROTEIN RECOGNIZES
SPECIFIC RECEPTORS SUCH AS PROTEIN,
CARBOHYDRATE OR LIPID ON THE OUTSIDE OF
THE CELL
THEREFORE, CELLS WITHOUT THE
APPROPRIATE RECEPTORS ARE NOT
SUSCEPTIBLE TO THE VIRUS
PENETRATION
VIRUS ENTERS THE CELLS IN A VARIETY OF
WAYS BASED ON ITS NATURE.
a)FUSING WITH THE PLASMA
MEMBRANE;
NUCLEIC ACID IS TO BE SUFFICIENTLY
UNCOATED BEFORE THE PROCESS CAN BEGIN
THIS WILL NOT ALLOW THE INFECTIOUS
VIRUS PARTICLES TO BE RECOVERED FROM THE
CELL
AND THIS STAGE LASTS UNTIL NEW VIRIONS
ARE MADE
Synthesis of Viral Nucleic Acid &
Protein
• Various virion components are synthesized
separately within the cell.
– Two stages of protein synthesis:
1. Transcription (Production of RNA from DNA)
2. Translation (assembly of protein by ribosomes, using
formation carried by RNA)
(RNA acts as a messenger)
• Then assembled to form progeny/descendant
particles.
Assembly/Maturation
• After finalization of the viral form, it starts to
assemble.
• There may be maturation step that follows
after the assembly process.
– Maturation step:
• Some of the assembled viral particles will bud off from
the host cell.
• The viral protein then process to mature and become
infectious.
Release
• Virus may be release due to cell lysis (destruction
of host cells).
• If it is enveloped
– It will bud out from the host cell.
• Budding viruses do not necessarily kill the host
cell.
– Thus, some budding viruses may be able to set up
persistent(constantly repeated) infections.
• Not all released viral particles are infectious
• The ratio of non-infectious to infectious particles
varies with the virus and the growth conditions.
Release
• Released through cell lysis (breaking open of the host
cell)
• If virus is enveloped, may bud from cell (form at the
cell surface and is pinched off)
• Budding viruses do not necessarily kill cell
• Hence, some budding viruses may set up persistent
infections
• Not all released viral particles are infectious
• Non infectious particles : Infectious particles varies
with virus and growth conditions
• Viruses produce disease through different
mechanisms which depends on the species
• At cellular level, it primarily include cell lysis which
cause death of the cell
• In multicellular organisms, whole organism may suffer
the effects if enough cells die
• Multiplication of viruses usually cause cell to be
damaged or die
• But, since they depend on host cell for their own
survival, they tend to produce milder infections rather
than causing the death of the cell
• Exceptions: HIV, ebola virus, rabiesvirus
Ebola virus:
• Damage and destroys blood vessel walls
• Prevent platelets from coagulating (clotting)
• Causes a viral hemorrhagic fever
• Symptoms: fever, bleeding disorder and may
progress to high fever, shock and even death
Rabies virus:
• Transmit through saliva of animals
• Infects central nervous system
• Cause disease in brain and death
Intracellular location:
• Advantage:- Protects virus against host’s immune
mechanism
• Disadvantage:- Makes the virus vulnerable
• Dependant on the host cell’s synthetic machinery
• Slightest physical/chemical change in the host cell
caused by the viral infection may alter the machinery
Rotaviruses
Affects mainly children
Spread through direct contact
HOWEVER..
They exist relatively harmless within an organism
Benefits:
Increase immune system’s response against infection by other pathogens
Herpes simplex virus - causes cold sores
Varicella zoster virus – causes chicken pox (Children)
Latent chicken pox infections – shingles (Adults)
The pathogenic virus remain in dominant state within the human body – It is called
virus LATENCY
USUALLY..
Viruses causes cells to proliferate
But does not cause malignancy
SOME VIRUSES..
Papillomaviruses
Established cause of cancer
Classification of viruses
Size and shape
Chemical composition
Structure of genome
Size and shape
• Viruses are usually
much smaller than
bacteria and are
submicroscopic
(cannot be seen
with a light
microscope)
• Most range in size
from 5 to 300
nanometers
Helical viruses
Helical filament of
• Helical – helical array of caspid
proteins (protomers) wrapped
around a helical filament of nucleic
acid
• Eg. Ebola virus, rabies virus
Icosahedron
Enveloped Viruses
• Enveloped - consist of nucleic acid
surrounded by either a helical or polyhedral
core and covered by an envelope
• Eg. Enveloped helical = Influenza virus
Enveloped polyhedral = Herpes simplex virus.
Enveloped helical
T-even bacteriophage
Poxvirus
Structure of genome
• The viral genome is a single or
segmented, circular or linear
molecule of nucleic acid
functioning as the genetic
material of the virus.
• It can be single-stranded or
double-stranded DNA or RNA
(but never both), and codes for
the synthesis of viral components
and viral enzymes for replication.
• Different genome requires
different replication strategies
1. Active prophylaxis
- Vaccination
2. Passive prophylaxis
Vaccination - Prevent infection by viruses
• Cheap
• Effective
- dramatic decline in illness & death
- infections previously deadly have been
..gotten rid of
Immune Response to Vaccines
• Vaccination evokes (call forth) an antibody
response
• Stimulates T lymphocytes
• Effectiveness measured by
1.% of recipients protected (most effective 90%)
2.Duration
3.Degree of protection(quantity)
Antibody – known as immunoglobin
- identifies and neutralizes foreign …………
…………...objects such as bacteria & viruses
T lymphocytes
• Identify specific antigens
• Generate specific responses to eliminate pathogen
( eg virus)
• Leave background of pathogen in form of ‘memory cells’
• Strong & rapid response the next round
Active Prophylaxis _ Produces own specific immunity
(Vaccines)
• Types of viral vaccines
• Greater protection
1. Attenuated live vaccine • Long-lasting protection
• Not suitable for
immunocompromised patients
&pregnant women