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Feline Immunodeficiency Virus Cell Entry

By Susan C. S. Frey, Edward A. Hoover and James I. Mullins

Abstract

The process of feline immunodeficiency virus (FIV) cell entry was examined using assays for virus replication intermediates. FIV subtype B was found to utilize the chemokine receptor CXCR4, but not CCR5, as a cellular receptor. Zidovudine blocked formation of late viral replication products most effectively, including circular DNA genome intermediates. Our findings extend the role of CXCR4 as a primary receptor for CD4-independent cell entry by FIV

Topics: Virus-Cell Interactions
Publisher: American Society for Microbiology
Year: 2001
DOI identifier: 10.1128/JVI.75.11.5433-5440.2001
OAI identifier: oai:pubmedcentral.nih.gov:114955
Provided by: PubMed Central
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