Please use this identifier to cite or link to this item: https://repository.seku.ac.ke/handle/123456789/193
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dc.contributor.authorNg'ang'a, Zipporah W.
dc.contributor.authorNyamache, Anthony K.
dc.contributor.authorMuigai, Anne W. T.
dc.contributor.authorKhamadi, Samoel A.
dc.date.accessioned2014-11-27T06:35:31Z
dc.date.available2014-11-27T06:35:31Z
dc.date.issued2012
dc.identifier.citationAIDS RESEARCH AND HUMAN RETROVIRUSES Volume 28, Number 8, 2012en_US
dc.identifier.urihttp://hdl.handle.net/123456789/193
dc.descriptionDOI: 10.1089/aid.2011.0122en_US
dc.description.abstractLittle is known about the extent and predictors of polymorphisms potentially influencing susceptibility to HIV integrase inhibitors. HIV-1 genetic diversity and drug resistance are major challenges in patient management globally. To evaluate HIV genetic diversity and drug resistance-associated mutations within a Nairobi cohort, genetic analysis of the HIV-1pol-integrase gene regions was performed on samples collected from 42 subjects and 113 Kenyan intergrase sequences deposited in the Los Alamos HIV database. From the partial pol-integrase sequences analyzed phylogenetically, it was shown that 26 (61.9%) were subtype A1, 9 (21.4%) were subtype D, 5 (11.9%) were subtype C, 1 (2.4%) was subtype A2 and 1 (2.4%) was subtype CRF. Integrase-associated mutations were found in 12 patients, and in all 113 sequences already deposited in GenBank. One sample from this study and five from previous Kenyan integrase sequences had mutations at T97A, which is associated with reduced susceptibility to raltegravir.en_US
dc.language.isoenen_US
dc.publisherMary Ann Liebert, Inc.en_US
dc.titleHIV type 1 genetic diversity and naturally occurring polymorphisms in HIV type 1 Kenyan isolates: implications for integrase inhibitorsen_US
dc.typeArticleen_US
Appears in Collections:School of Science and Computing (JA)

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