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<categorytree mode=pages>Retroviridae</categorytree>
 
<categorytree mode=pages>Retroviridae</categorytree>
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BLV-HTLV retroviruses
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:''Bovine Leukosis Virus''
      
|logo =FeLV logo.jpg
 
|logo =FeLV logo.jpg
 
}}
 
}}
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==Morphology==
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{{Learning |Vetstream = <p>[https://www.vetstream.com/felis/Content/Bug/bug60015.asp Feline Immunodeficiency Virus]</p><p>[https://www.vetstream.com/felis/Content/Bug/bug60014.asp Feline Leukemia Virus]</p>}}
*Fragile, enveloped RNA viruses with roughly spherical spike proteins
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*Genome has 3 genes:
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**''gag'': group-specific antigen coding gene, encodes capsid proteins
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**''pol'': encodes reverse transcriptase (RT) and integrase
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**''env'': encodes envelope spikes, and can be used in diagnosis and subunit vaccines
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*Both ends of genome show a promoter (LTR: long terminal repeat)
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==Antigenicity==
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*Group-specific antigens (gag's) are shared by all isolates of each virus
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**This can be exploited by diagnostic tests
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*Lentiviruses show variation by mutation, making vaccination difficult
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==Virulence and Pathogenesis==
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*Replication involves integrating into the host cell genome:
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**'''Uncoating''' to release RNA and RT
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**+RNA '''transcribed''' to -DNA by RT
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**-DNA becomes circular dsDNA and is '''integrated''' into host chromosome by integrase
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**DNA '''codes''' for viral proteins using cellular organelles and enzymes
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**Because of this technique, virus replication is much '''slower''', and retroviruses can remain '''latent'''
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*Tumor production takes 2 forms:
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**Viruses can carry oncogenes within their genome --> tumor production occurs quickly
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**Insertion of the viral LTR switches on proto-oncogenes in the host cell genome --> tumor production can take years
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[[Category:Viruses]][[Category:To_Do_-_Viruses]]
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[[Category:Viral Organisms]]
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[[Category:To_Do_-_Clinical/Viruses]]
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