DSpace
 

University of Jos Institutional Repository >
Natural Sciences >
Microbiology >

Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/885

Title: HIV Subtype and Drug Resistance Patterns Among Drug Naïve Persons in Jos, Nigeria
Authors: Lar, P.
Lar, N.
Bemis, K.
Jelpe, J.
Enzyguirre, L.
Ayuba, L.
Zella, D.
Kanki, P.
Carr, J. K.
Blattner, W.
Abimiku, A. G.
Keywords: Characterization
CRF02_AG
baseline
niverapine
Unique Recombinant Forms
West Africa
Issue Date: 20-Aug-2007
Publisher: African Journal of Biotechnology
Series/Report no.: Vol. 6;No. 16; Pp. 1892-1897
Abstract: To determine HIV-1 subtypes and antiretroviral drug resistance mutations for 16 infected, pregnant women in Jos, Nigeria, part of pol (1040 bp) was amplified from patient PBMC DNA, sequenced and analyzed. Eight of the samples were subtype G, three were CRF02_AG and 2 were unique recombinant forms (URF) between G and CRF02_AG. The remaining consisted of 3 different strains: one was subtype C, and the other 2 were unrelated URF. Nearly full-length genome sequences were completed for 6 of the strains: 4 subtype G and 2 CRF02_AG. In the 14 drug-naïve subjects, no primary resistance-associated mutations were found, but secondary mutations were identified in 7 different codons of the gene coding for protease: PR K20I, M36I, L63A/P/V, V82I, L10M/I and I93L. In addition, the K238R mutation was identified in the reverse transcriptase gene of 3 viruses. The PR K20I and M36I mutations occurred in all of the strains, and the L10M and V82I mutations occurred only in subtype G. The mutation, I93L, was carried by subtype C viruses. Two of the women that had prior niverapine treatment, had primary resistance-associated mutations, RT M184V and K103N, archived in their proviral DNA several months after treatment cessation. The study reports a predominance of clade G and CRF02_AG, and provides many more examples of nearly full-length genome sequences for subtype G viruses from Nigeria. The ubiquitous presence of PI secondary resistance-associated mutations, as well as primary resistanceassociated mutations in 2 previously treated women, underscores the need to ensure adherence compliance to treatment.
URI: http://hdl.handle.net/123456789/885
ISSN: 1684–5315
Appears in Collections:Microbiology

Files in This Item:

File Description SizeFormat
article1379923299_Lar et al.pdf224.34 kBAdobe PDFView/Open
View Statistics

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

 

Valid XHTML 1.0! DSpace Software Copyright © 2002-2010  Duraspace - Feedback