Molecular surveillance of HIV-1 field strains in Nigeria in preparation for vaccine trials

被引:29
作者
Agwale, SM
Zeh, C
Robbins, KE
Odama, L
Saekhou, A
Edubio, A
Njoku, M
Sani-Gwarzo, N
Gboun, MS
Gao, F
Reitz, M
Hone, D
Pieniazek, D
Wambebe, C
Kalish, ML
机构
[1] Ctr Dis Control & Prevent, Atlanta, GA 30333 USA
[2] Inst Human Virol, Div Vaccine Res, Baltimore, MD USA
[3] Natl Inst Pharmaceut Res & Dev, Abuja, Nigeria
[4] Univ Jos, Jos, Nigeria
[5] Fed Minist Hlth, Abuja, Nigeria
[6] Univ Alabama, Birmingham, AL USA
关键词
HIV-1; molecular epidemiology; vaccine; Nigeria;
D O I
10.1016/S0264-410X(02)00059-2
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We conducted a national molecular epidemiologic survey of HIV-1 strains in Nigeria to determine the most prevalent subtype(s) for use in developing candidate vaccines. A total of 230 HIV-1-positive blood samples collected from 34 of the 36 Nigerian states were analyzed by our modified env gp41-based heteroduplex mobility assay (HMA) and/or gp41 sequencing and analysis. Overall, 103 (44.8%) were subtype A, 125 (54.3%) were subtype G, one (0.4%) was subtype C. and one (0.4%) was subtype J, and one (0.4%) was unclassifiable, To further characterize Nigerian viruses to aid in strain selection for candidate vaccines, one gp41 subtype G and five gp41 subtype A strains were selected for full envelope sequencing. The one subtype G sequence had consistent phylogenies throughout gp 160. using programs to detect recombination. However, all five sequences that were primarily subtype A in gp41 were found to be recombinant viruses. Two of the five (40%) were A/G/J mosaics with common breakpoints. The remaining three gp 160 recombinants all had their own unique break points: two A/? and one A/?/G,however, all five had the majority of their mosaic breakpoints occurring in gp41. None of the five were consistent with the circulating recombinant form (CRF)O2_AG strain previously reported to be prevalent in West Africa. In conclusion, we showed a clear dominance and widespread distribution of gp41 subtypes A and G in fairly equal proportions, suggesting that vaccines designed for use in this geographic locale should incorporate the gene(s) of both subtypes. However, appreciating the magnitude of diversity of HIV-1 strains in Nigeria may require sequencing and analysis of longer gene regions for the identification of prevalent or emerging CRFs. Published by Elsevier Science Ltd.
引用
收藏
页码:2131 / 2139
页数:9
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