viral classification

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    Virology

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    Classification of Virus

    Two main schemes:

    ICTV (International Committee on Taxonomy of

    Viruses )

    Baltimore : (Developed by David Baltimore)

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    ICTV

    It is a universal code for viral classification

    The essential principles of virus nomenclature

    are:-

    To aim for stability.

    To avoid or reject the use of names which might

    cause error or confusion.

    To avoid the unnecessary creation of names

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    Virus classification system shall employ the hierarchicallevels of Order: A group of families sharing certain common characters.

    An order name must be a single word ending in virales

    Family: A group of genera or subfamilies, sharing certaincommon characters. A family name must be a single wordending in viridae

    Subfamily: A group of genera sharing certain commoncharacters. The taxon shall be used only when it is needed to

    solve a complex hierarchical problem. A subfamily name mustbe a single word ending in virinae.

    Genus: A group of related species that share some significantproperties and often only differ in host range and virulence. Agenus name must be a single word ending in virus.

    Species: A virus species is defined as a polythetic class of virusesthat constitutes a replicating lineage and occupies a particularecological niche.

    According to ICTV 2011 report there are 6+1 orders, 94families, 22 subfamily, 395 genera and 2480 species.

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    Caudovirales : Tailed dsDNA (group I) bacteriophages.

    Herpesvirales: Large eukaryotic dsDNA viruses.

    Mononegavirales : Nonsegmented (-) strand ssRNA plantand animal viruses.

    Nidovirales : (+) strand ssRNA viruses with vertebratehosts.

    Picornavirales: Small (+) strand ssRNA viruses that infecta variety of plant, insect and animal hosts.

    Tymovirales: Monopartite (+) ssRNA viruses that infectplants.

    Ligamenvirales: infecting archaea has been proposed.

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    Baltimore Baltimore system classify virus based on type of genome

    and strandedness

    There are 7 groups according to Baltimore classification

    I: dsDNA viruses (e.g. Adenoviruses, Herpesviruses,Poxviruses)

    II: ssDNA viruses (+)sense DNA (e.g. Parvoviruses)

    III: dsRNA viruses (e.g. Reoviruses)

    IV: (+)ssRNA viruses (+)sense RNA (e.g. Picornaviruses,Togaviruss)

    V: ()ssRNA viruses()sense RNA (e.g. Orthomyxoviruses,Rhabdoviruses)

    VI: ssRNA-RT viruses (+)sense RNA with DNA intermediatein life-cycle (e.g. Retroviruses)

    VII: dsDNA-RT viruses (e.g. Hepadnaviruses)

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    Fine structure of Virus

    Capsid with(out) Envelope

    Protect virus from physical, chemical and bilogical

    damage

    Helps virus to attach on the host

    Mostly Capable of self assembly

    Nucleic acid

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    Helical Capsid

    Fraenkel-Conrat & Williams showed that

    when mixtures of purified tobacco mosaic

    virus (TMV) RNA & coat protein wereincubated together, virus particles formed

    The fact that helical symmetry is a useful

    way of arranging a single protein subunit to

    form a particle is confirmed by the largenumber of different types of virus which

    have evolved with this capsid arrangement.

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    Icosahedral (isometric) capsids

    Simplest known icosahedaral virus are

    bacteriophage X174

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    Enveloped viruses

    Matrix Proteins: These are internal virion

    proteins whose function is effectively to linkthe internal nucleocapsid assembly

    Glycoproteins: These are transmembrane

    proteins, anchored to the membrane by a

    hydrophobic domain

    External Glycoproteins

    Transport Channels

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    Complex Virus Structures

    Pox virus Tailed phages

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    Life cycle of VIrus

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    Attachment

    Penetration & Release

    Biosynthesis Immediate Early Genes : Early phase proteins

    Delayed Early Genes : Middle phase

    Late Genes : Late phase

    Assembly

    Release

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    PRION (INfectious PROtein)

    Prions are mis-folded proteins (PrpSC)

    Responsible for the transmissiblespongiform encephalopathies

    They are formed from a normalproteins called PrPc

    PrP play important roles in cell-celladhesion and intracellular signaling invivo, and may therefore be involvedin cell-cell communication in thebrain

    Completely digested by Proteinase K

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    Prion Infection

    PrPsc is an isoform of PrPc

    Infection of PrPsc from another animal

    Genetic factor (PRPN gene mutation)

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    Growth of Prions

    two models

    1. Heterodimer

    2. fibril model

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    Characteristics of Prion

    Highly resistant to chemical and physical

    treatments

    Can aggregate by simply transforming the

    normal proteins

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    Diseases due to prion

    Initiated when a prion agent aenter in the

    system through digestive tract.

    Then they move to lymph system and multiply

    Slowly it starts accumulating in the neurons

    Eg. Find out by yourself

    Assignment: Protein only hypothesis

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