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