Virus
Properties
• Infectious – must be transmissible
horizontally
• Intracellular – require living cells
• RNA or DNA genome, not both
• Most all have protein coat
• May of may not have lipid envelope
• May have broad or narrow host range
• Adsorption, entry, uncoating,
replication, assembly, release.
• Use host factors for to complete
replication cycle
Composition
of viruses infecting different hosts
• No “rules” about virus families that
may or may not be present in a given kingdom.
• Some types of viruses are found more
commonly in some kingdoms than in others.
– Many plant viruses contain ssRNA
genomes
– Many fungal viruses contain dsRNA
genomes
– Many bacterial viruses contain dsDNA
genomes
• Host properties determine the types
of viruses that tend to be found in members of a biological “kingdom”
Overview
of Virus Properties
• Animal
– RNA – 5-30 kb
– DNA: 5-350 kb
– Many enveloped
– Range of complexity
– Range of morphologies
– Some divided genomes
• Prokaryote
– RNA – 5-8 kb
– DNA
– 10-200 kb
– Few enveloped
– Range of complexity
– Range of morphologies
– Few divided genomes
• True
Fungi
– RNA
– 2.5-28 kb
– DNA – none
– Enveloped
– Little genome complexity
– Little morphological complexity
– Some divided genomes
• Plant
– RNA
– 0.3-28 kb
– DNA – 3-10 kb
– Few enveloped
– Little genome complexity
– Little morphological complexity
– Many divided genomes
• Lower eukaryote
– RNA – 5-10 kb
– DNA
– 180-1200 kb
– Envelope
– Range of complexity
– Range of morphologies
– No divided genomes
Tobacco
mosaic virus – a typical small RNA virus
• 18X300 nm
• Single 6400 nt RNA
• 2130 molecules of single 17
kDa coat protein.
• 3 essential genes.
• Simple regulatory elements.
Poxvirus
– a typical large dsDNA virus
• 120X200 nm
• Single 180 kb DNA
• Complex coat made up of numerous proteins
• >100 essential genes
• Complex regulatory elements
Virus at
the edge: Mimivirus
• Acantamoeba polyphaga Mimivirus (APMV)
• 400 nm particle, 1.2 megabase genome, dsDNA
virus
• Represent the 3rd largest virus identified
yet
• Many genes for normal cellular functions
• Mimivirus (mimicking
microbe)
• Mistakenly thought to be a gram-positive
bacterium.
• Placed at the boundary of living and
non-living.
• Has genes for nucleotide and amino acid
synthesis.
• Does not exhibit many characteristics,
including genes for ribosomal proteins, etc.
Naming
viruses
Animal
viruses
1. Diseases that they cause: small pox, foot
and mouth disease, hepatitis
2. Places where virus was first identified
Norwalk virus, West Nile virus, Hanta virus
3. Other
1. Organ virus was isolated from:
adenoids-Adenovirus
Sin Nombre
Plant
viruses and many insect viruses (two components)
1) Host
2) Disease
Tomato bushy stunt virus
Cricket paralysis virus
Classification of Viruses
Classical: morphology
Physical and chemical composition
Genetic relatedness
Modern: Phylogenetic, based on nucleic
acid sequence analysis.
Classical criteria for classification of animal viruses
• Several parameters are used for
classification
– Type of genomic nucleic acid
– Size of virion and genome
– Capsid structure
– Host
– Replication mechanism
All these approaches fail to predict
fundamental features of the viruses.
Problem
in Viral Classification
• Similar disease, but different viruses
o Hepatitis A virus: a Picornavirus
o Hepatitis B virus: a Hepatoavirus
o Hepatitis C virus: a Flavivirus
• Similar viruses, but different diseases
o HSV 1: Cold sores
o HSV 2: Genital Lesions
o VZV: Chicken Pox
o CMV: Organ Failure
o EBV: Mononucleosis, Burkitt’s Lymphoma
So simple classification system did not work
well. Virologists had to devise more orderly systems.
Modern Criteria for classification
The
Baltimore classification system
Based on genetic contents and replication
strategies of viruses.
According to the Baltimore classification,
viruses are divided into the following seven classes:
1. dsDNA viruses
2. ssDNA viruses
3. dsRNA viruses
4. (+) sense ssRNA viruses (codes directly
for protein)
5. (-) sense ssRNA viruses
6. RNA reverse transcribing viruses
7. DNA reverse transcribing viruses where
"ds" represents "double strand" and "ss" denotes
"single strand".
Comparisons
of Vertebrate and Plant Viruses
Classification and Nomenclature
ICTV-International Committee on Taxonomy of
Viruses (meets every 3 years).
Considerations:
– Host range (eukaryote or prokaryote,
animal, plant etc.)
– Morphological features (enveloped, shape of
capsid)
– Nature of genome
Taxonomy scheme
Total
Family: 87
Subfamily: 19
Genus: 348
Species: 2290
Characteristics
of the ICTV system
• “Non-systematic”
• Polythetic
• Employ hierarchical level to species as
lowest level
• Universal
• Limited (very conservative)
• Latinized, but no binomials
• Preserves common or trivial names at
species level
Family
• A group of genera with common
characteristics.
• Capitalized, Italicized, and end in -viridae.
Examples:
– Picornaviridae (picornavirus family
is also acceptable).
– Herpesviridae (herpesvirus family).
– Flaviviridae (flavivirus family)
Origins
of family names
Herpes: produce scaly (snake
skin) lesions
Pox: infections produce pox
lesions
Papilloma: infections result in
papilla (bumps on skin), e.g. warts
Flavi: Latin for yellow
2) Sites of infection
Adeno: infections of
respiratory tract
Picorna: Pico (small) + RNA
Corona: wearing a crown
Filo: Look fibrous
4) Combination
Hepadna: hepatitis + DNA
Subfamilies
• Groups within some large families. To solve
a complex hierarchical problem.
• Capitalized, Italicized, end in -virinae.
• Examples
– Alphaherpesvirinae
– Betaherpesvirinae
– Gammaherpesvirinae.
Genus
• A group of virus species sharing common
characteristics.
• Capitalized, Italicized, ends in -virus.
Type member: a single virus designated by the
ICTV that serves as a reference for the genus
Example from Flaviviridae:
• Flavivirus-yellow fever virus
• Pestivirus- Bovine Diarrhea virus 1
• Hepacivirus-Hepatitis virus C (HCV)
Species
• A cluster of strains from a variety of
sources or a population of strains from one particular source, all of which
have in common a set pattern of stable properties that separates the cluster
from other clusters or strains.
• Not capitalized.
• Not italicized.
Examples:
– Poliovirus
– Human immunodeficiency virus
– West Nile virus
Taxonomy: two examples
Example
1: herpes simplex virus 1
_ Family: Herpesviridae or herpesvirus
family
_ Subfamily: Alphaherpesvirinae;
_Genus: Simplexvirus;
» Species: herpes simplex virus 1.
Example
2: Poliovirus
_ Family: Picornaviridae or
picornavirus family;
_ Subfamily: None;
_Genus: Enterovirus;
» Species: poliovirus
Further breakdowns not recognized by the
ICTV
• Strain- different lines of isolates
of the same virus.
– Example: Isolated from different
geographical locations.
• Type- different serotype (different
antigenic specificity) of the same virus.
– Example: Influenza type A or B. There may
also be “subtypes” within a particular type.
• Group- sub-category of species, division
often based on genomic sequence similarities or origin.
– Example: HIV group M (Main), N (Neither M
or O), or O (Outlier).
– There may also be “subgroups” (sometimes
called clades) within a particular group (subgroups A-J of group M HIV).
• Variant-Virus whose phenotype
differs from original wild type strain but where the genetic basis for the
difference is not known.
Satellite virus
Common features:
1) Do not encodes enzymes required for
replication.
2) Therefore require co-infection with a
conventional (helper) virus
3) Satellite genome is significantly
different from the helper virus
4) May affect replication of the helper
virus.
5) May increase or decrease severity of
disease
Satellites
viruses
Encodes structural proteins, which form the
viral capsid
They rely on the helper virus replicative
machinery to replicate their genomes.
Examples: adeno associated virus (helper:
adenovirus)
DI Particles
Defective interfering particle: A virus that
lacks part of its genome and interferes with the replication of a standard
virus.
1. Require helper virus
2. Derived from helper virus: They tend to be
deletion mutants that have lost their ability to encode proteins, but retain
their ability to be replicated by the helper virus replicative machinery. (defective)
3. Interfere
with
helper virus replication by their ability to out compete for helper virus
resources.
Viroids:
Novel agent of disease in plants
• Single circular ssRNA molecule with no
protein component
• High complementary (70% base-paired)
• Extremely small in size ranges from 246-267
nucleotides
• Disease from RNA interfering with essential
host cell mechanisms
• Viroids RNA does not code for any protein.
• Long been a confusion over how viroids are
able to produce symptoms without encoding any protein.
• They are cleaved by dicer enzymes into small
interfering
RNAs (siRNAs).
• siRNA sequences are capable of
complementary base pairing with plant’s own mRNA.
• Induction of degradation or inhibition of
translation is what causes the symptoms of classic viroid infection.
Prions
- Prions are single molecules containing
about 250 amino acids.
- They are abnormal variants of proteins
which normally occur in cells.
- Prions have the ability to convert the
normal forms that they come into contact with into abnormal forms
Prion
Hypothesis
• PrP is a normal cellular protein referred
to as PrPc
• Diseased brain contains aberrant PrP which
is referred to as
PrPSc . PrPSc has the ability to convert PrPc
to itself.
• A chain reaction follows, resulting in a
cluster of tangled, nonfunctional proteins called plaques, which are aggregates
of PrPSc in the brain.
• The body defences remove these PrPSc aggregates
leaving behind holes.
• This causes degeneration of the brain cells
leading to mental changes and ultimately, death.
Transmission
• Prion in cattle is mainly are from the carcasses
of scrapie-infected sheep.
• After these infected sheep having died
their brains and other sheep byproducts infected with scrapie is used to feed
cattle with the meat and bone meal (MBM).
• Feeding cattle animal bi-products such as
meat-n-bone meal that has an infected prion causes the infection in the cattle.
• The prions are concentrated in the brain,
and spinal cord of these animals.
• There is no evidence that it is
concentrated in the muscle mass of cattle, and they are considered safe as long
as they are not in contact with the brain and spinal cord during the slaughter
process.
• Sheep with Scrapie used in Meat and Bone
Meal
(MBM) – known as “Offal”
• MBM fed to cattle.
• Infected Beef eaten by humans
– When cattle brains and other cattle
byproducts infected with BSE are ingested by humans, there is a risk of the
Creutzfeldt Jakob Disease.
– Not affected by cooking.
– One person per million worldwide each year.
– New Guinea cases in 1900, due cannibalism.
Transmissible Spongiform Encephalopathies
_ The Mad Cow Disease in Cows, Scrapie
in Sheep, the Creutzfeldt-Jakob Disease in human beings belong to a class
of disease called Transmissible Spongiform
Encephalopathy (TSEs)
_ Initially thought to be due to “slow
viruses”, due to the long incubation period between time of infection and appearance
of disease, these are now known to be caused by agents called prions.
_ Transmissible Spongiform Encephalopathy
(TSEs) are rare forms of progressive neurodegenerative disorders that affect
both humans & animals
Transmissible
Spongiform Encephalopathies
_ It is found on any type of cloven hoofed
animals such as: pigs, sheep, and cattle
_ Scientific
Name:
_In cows: Bovine Spongiform Encepalopathy
(BSE)
_In Sheep: Scrapie Spongiform Encepalopathy
(SSE)
_In human: Creutzfeldt-Jakobs Disease (CJD)
Transmissible
Spongiform Encephalopathies
• Transmissible Spongiform Encephalopathy
(BSE) is so named because of the spongy appearance of the brain tissue of
infected cattle (and also in the human beings) when sections are examined under
a microscope
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