TY - JOUR
T1 - Monitoring HIV-1 group M subtypes in Yaoundé, Cameroon reveals broad genetic diversity and a novel CRF02-AG/F2 infection
AU - Courtney, Colleen R.
AU - Agyingi, Lucy
AU - Fokou, Arlette
AU - Christie, Stephanie
AU - Asaah, Bladine
AU - Meli, Josephine
AU - Ngai, Johnson
AU - Hewlett, Indira
AU - Nyambi, Phillipe N.
N1 - Publisher Copyright:
© Mary Ann Liebert, Inc. 2016.
PY - 2016/4/1
Y1 - 2016/4/1
N2 - Broad HIV-1 genetic diversity in Cameroon provides a unique opportunity to monitor HIV-1 evolution and allows the detection of novel strains. We have genetically characterized the HIV-1 subtypes found in 156 samples from 90 drug-naive subjects in Yaoundé, Cameroon collected from 2011 to 2013, using phylogenetic analysis of regions in gag and pol. We identified subtypes CRF02-AG (64.9%), CRF22-01A1 (7.1%), D (4.5%), F2 (3.9%), G (3.2%), CRF18-cpx (3.2%), CRF37-cpx (3.2%), CRF11-cpx (2.6%), CRF13-cpx (1.9%), A1 (1.3%), CRF01-AE (1.3%), CRF09-cpx (1.3%), A2 (0.6%), and H (0.6%). Sequence data for both the gag and pol regions were obtained from 62 subjects; for 59 of these subjects the two regions were identified as the same viral subtype while three subjects were discordant, A1/CRF02-AG (subject MDC006), CRF02-AG/F2 (subject MDC179), and a dual infection with CRF02-AG/F2 (subject MDC131). Longitudinal sequence data were obtained for 28 of these 62 subjects and confirmed the cross-sectional results. These data update subtype information for this area and highlight the necessity of such studies due to the numerous circulating subtypes, the ongoing superinfection, and the risk of emerging novel recombinant viruses.
AB - Broad HIV-1 genetic diversity in Cameroon provides a unique opportunity to monitor HIV-1 evolution and allows the detection of novel strains. We have genetically characterized the HIV-1 subtypes found in 156 samples from 90 drug-naive subjects in Yaoundé, Cameroon collected from 2011 to 2013, using phylogenetic analysis of regions in gag and pol. We identified subtypes CRF02-AG (64.9%), CRF22-01A1 (7.1%), D (4.5%), F2 (3.9%), G (3.2%), CRF18-cpx (3.2%), CRF37-cpx (3.2%), CRF11-cpx (2.6%), CRF13-cpx (1.9%), A1 (1.3%), CRF01-AE (1.3%), CRF09-cpx (1.3%), A2 (0.6%), and H (0.6%). Sequence data for both the gag and pol regions were obtained from 62 subjects; for 59 of these subjects the two regions were identified as the same viral subtype while three subjects were discordant, A1/CRF02-AG (subject MDC006), CRF02-AG/F2 (subject MDC179), and a dual infection with CRF02-AG/F2 (subject MDC131). Longitudinal sequence data were obtained for 28 of these 62 subjects and confirmed the cross-sectional results. These data update subtype information for this area and highlight the necessity of such studies due to the numerous circulating subtypes, the ongoing superinfection, and the risk of emerging novel recombinant viruses.
UR - https://www.scopus.com/pages/publications/84962440412
U2 - 10.1089/aid.2015.0286
DO - 10.1089/aid.2015.0286
M3 - Article
C2 - 26681241
AN - SCOPUS:84962440412
SN - 0889-2229
VL - 32
SP - 381
EP - 385
JO - AIDS Research and Human Retroviruses
JF - AIDS Research and Human Retroviruses
IS - 4
ER -