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dc.contributor.authorNovitsky, Vladimir
dc.contributor.authorWang, Rui
dc.contributor.authorBaca, Jeannie
dc.contributor.authorMargolin, Lauren
dc.contributor.authorMcLane, Mary F.
dc.contributor.authorMoyo, Sikhulile
dc.contributor.authorWidenfelt, Erik van
dc.contributor.authorMakhema, Joseph
dc.contributor.authorEssex, M.
dc.date.accessioned2019-10-15T18:22:17Z
dc.date.issued2011
dc.identifier.citationNovitsky, Vladimir, Rui Wang, Jeannie Baca, Lauren Margolin, Mary F. McLane, Sikhulile Moyo, Erik van Widenfelt, Joseph Makhema, and M. Essex. 2011. “Evolutionary Gamut of in Vivo Gag Substitutions during Early HIV-1 Subtype C Infection.” Virology 421 (2): 119–28. https://doi.org/10.1016/j.virol.2011.09.020.
dc.identifier.issn1178-122X
dc.identifier.urihttp://nrs.harvard.edu/urn-3:HUL.InstRepos:41552036*
dc.description.abstractTwo analyses of HIV-1 subtype C Gag quasispecies were performed in a prospective cohort of 42 acutely and recently infected individuals by SGA on viral RNA/proviral DNA templates. First, in vivo Gag substitutions were assessed in relation to the HIV-1C consensus sequence, which revealed that 29.3% of detected amino acid substitutions can be classified as reversions to subtype consensus, 61.3% as forward substitutions from subtype consensus, and 9.3% as polymorphisms not associated with the subtype consensus sequence. Second, the proportion, dynamics, and relationships within individual pools of viral quasispecies were analyzed. Among reverse substitutions, 16.1% were minor, 11.0% transient, 13.6% dominant, and 59.2% fixed. In contrast, 31.6% of forward substitutions were minor, 59.3% transient, 3.8% dominant, and 5.3% fixed. The distinct patterns in the spectrum and dynamics of reverse and forward Gag substitutions suggest that these differences should be considered in HIV-1 evolutionary studies and analyses of viral mutational pathways.
dc.language.isoen_US
dc.publisherSAGE Publications
dash.licenseLAA
dc.titleEvolutionary Gamut of in vivo Gag Substitutions during Early HIV-1 Subtype C Infection
dc.typeJournal Article
dc.description.versionAccepted Manuscript
dc.relation.journalVirology - Research and Treatment
dash.depositing.authorWang, Rui::bf1a234ca95ae1f0959d1c158d4f8aa4::600
dc.date.available2019-10-15T18:22:17Z
dash.workflow.comments1Science Serial ID 115885
dc.identifier.doi10.1016/j.virol.2011.09.020
dash.source.volume421;2
dash.source.page119


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