e xit of virions from cells

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LECTURE 15:. E xit of virions from cells. Viro100: Virology 3 Credit hours NUST Centre of Virology & Immunology. Waqas Nasir Chaudhry. Formation of virion membranes. Enveloped virions acquire their membrane envelopes by one of two mechanisms ; - PowerPoint PPT Presentation

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Exit of virions from cells

Exit of virions from cellsLECTURE 15:Viro100: Virology3 Credit hoursNUST Centre of Virology & ImmunologyWaqas Nasir Chaudhry

1Formation of virion membranesEnveloped virions acquire their membrane envelopes by one of two mechanisms;

Either they modify a host cell membrane and then nucleocapsids bud through itThe virus directs synthesis of new membrane, which forms around the nucleocapsidsBudding through cell membranesMost enveloped viruses acquire their envelopes by budding through a membrane of the host cellRegions of membrane through which budding will occur, become modied by the insertion of one or more species of virus protein, the vast majority of which are glycoproteinsCell proteins may not be totally excluded from these regions and may become incorporated into virus envelopes; for example, HIV envelopes contain major histocompatibility complex class II proteins

Budding of virions involves interaction between the cytoplasmic tail of a virus glycoprotein in the membrane and another virus protein.M (membrane, matrix) proteinM proteins have an afnity for membranes, and bind to nucleocapsids as well as to the virus glycoproteins, stitching the two together during budding.The vital role played by the M protein in the budding process has been demonstrated using mutants of measles virus (a paramyxovirus) and rabies virus (arhabdovirus).

Roles similar to that of the M protein are played by the M1 protein of inuenza A virus and the MA (matrix) domain of the retrovirus Gag protein

Viruses that bud from the cell do so from particular regions of the plasma membrane, and if the cell is polarized then budding may take place primarily from one surface.

Membrane trafficking pathways within the host cellDe novo synthesis of viral membranesA minority of viruses direct the synthesis of lipid membrane late in the replication cycle.In some cases the membrane forms a virion envelope (e.g. poxviruses); In other cases the membrane forms a layer below the surface of the capsid (e.g. iridoviruses)Baculoviruses produce two types of enveloped virion during their replication. One type of virion has the function of spreading the infection to other cells within the host, and this virion acquires its envelope by budding from the plasma membrane.The other type of virion has the function of infecting new host individuals. Its envelope is laid down around nucleocapsids within the nucleus and the resulting virions become incorporated into occlusion bodies

Virion exit from the infectedcellThe virions of many viruses are released from the infected cell when it bursts (lyses), a process that may be initiated by the virus.Many phages produce enzymes (lysins, such as lysozymes) that break bonds in the peptidoglycan of the host bacterial cell walls.Other phages synthesize proteins that inhibit host enzymes with roles in cell wall synthesis; this leads to weakening of the cell wall and ultimately to lysis

Phage Lysins as Novel Alternatives to Antibiotics; Prof. Dr. Vincet FischettiBecause of their modes of transmission, most plant viruses leave their host cells in ways that differ from those of animal and bacterial viruses.Plant cells are separated from each other by thick cell walls, but in many of them there are channels, called plasmodesmata, through which the plant transports materials.Viruses are able to spread within the host by passing from cell to cell through plasmodesmata.

Spread of plant viruses through plasmodesmetaFor spread to new hosts many plant viruses leave the host cell as a component of the meal of a vector (e.g. an aphid or a nematode) that feeds by ingesting the contents of cells

They are dsRNA viruses which replicate in the cytoplasm (indicating they have everything they need for replication and do not utilize the cells replication enzymes) and they do not fully uncoat during the process of replication. The reason for their failure to fully uncoat is that the coat is resistant to protease digestion, which prevents them from being completely destroyed by the infected cell. The mRNA used in translation is synthesized from the negative strand of the dsRNA. Each negative strand produces many positive strands. The process utilizes particle-associated transcriptase. Neither of the strands of dsRNA appear among the transcription products, and both strands remain in the uncoated core particle. Reviridae Genome Replication; Conservative mode

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