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pubmed-article:12376757pubmed:abstractTextThe nef genes of human and simian immunodeficiency viruses code for a membrane associated protein critical for AIDS development. SIVmac Nef presents C-terminal a 27 amino acid extension absent of HIV-1 Nef. To estimate the influence of this C-terminal domain on virus properties, we constructed viruses derived from SIVmac239 by replacing SIV nef with HIV-1 Lai nef gene (SHIV NefLai4) or with a sequence encoding a Nef fusion protein: HIV-1 Lai Nef/SIV Nef-Cterm (SHIV-Cterm). The recombinant viruses replicated efficiently in vitro in CEMx174 cells and in activated macaque PBMCs. The addition of SIV Nef C-terminal domain to HIV-1 Nef in SHIVNefLai4 did not change the in vitro properties of the chimeric virus, both viruses being more infectious than a nef deleted virus. Although the half-life of Nef fusion protein was augmented, SHIV-Cterm remained slightly less infectious than SIVmac239.lld:pubmed
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pubmed-article:12376757pubmed:dateRevised2007-11-15lld:pubmed
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pubmed-article:12376757pubmed:articleTitleProperties of a chimeric simian-human immunodeficiency virus expressing an hybrid HIV-1 Nef/SIVmac Nef protein.lld:pubmed
pubmed-article:12376757pubmed:affiliationINSERM U544, Institut de Virologie, Université Louis Pasteur, Strasbourg, France.lld:pubmed
pubmed-article:12376757pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:12376757pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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