TY - JOUR
T1 - Human leukocyte antigen-associated hiv-1 crf02_ag gag and vif polymorphisms in ghana
AU - Adusei-Poku, Mildred A.
AU - Matsuoka, Saori
AU - Bonney, Evelyn Y.
AU - Abana, Christopher Z.
AU - Duker, Ewurabena O.
AU - Nii-Trebi, Nicholas I.
AU - Ofori, Sampson B.
AU - Mizutani, Taketoshi
AU - Ishizaka, Aya
AU - Shiino, Teiichiro
AU - Kawana-Tachikawa, Ai
AU - Ishikawa, Koichi
AU - Ampofo, William K.
AU - Matano, Tetsuro
N1 - Publisher Copyright:
© 2019, National Institute of Health. All rights reserved.
PY - 2019
Y1 - 2019
N2 - In human immunodeficiency virus type-1 (HIV-1) infections, cytotoxic T-lymphocyte (CTL) responses targeting human leukocyte antigen (HLA)-restricted viral epitopes exert strong suppressive pressure on viral replication and frequently select for mutations resulting in viral escape from CTL recognition. Numerous data on these HLA-associated mutations in HIV-1 subtypes B and C have been amassed with few reports described in other subtypes. In the present study, we investigated the HLA-associated mutations in HIV-1 subtype CRF02_AG prevailing in Ghana, Western Africa. We determined viral gag sequences in 246 out of 324 HIV-1-infected Ghanaians. Phylogeny analysis revealed that 200 (81.3%) individuals were infected with HIV-1 CRF02_AG. Full gag and vif sequences were obtained from 199 and 138, respectively, out of the 200 individuals infected with CRF02_AG and subjected to determination of HLA-associated mutations. The analysis found HLA-associated HIV-1 CRF02_AG non-synonymous polymorphisms at 19 sites; 13 in gag and six in vif, including those that were newly determined. Generation of this data is an important contribution to our understanding of HIV-1 CRF02_AG and host T cell interaction.
AB - In human immunodeficiency virus type-1 (HIV-1) infections, cytotoxic T-lymphocyte (CTL) responses targeting human leukocyte antigen (HLA)-restricted viral epitopes exert strong suppressive pressure on viral replication and frequently select for mutations resulting in viral escape from CTL recognition. Numerous data on these HLA-associated mutations in HIV-1 subtypes B and C have been amassed with few reports described in other subtypes. In the present study, we investigated the HLA-associated mutations in HIV-1 subtype CRF02_AG prevailing in Ghana, Western Africa. We determined viral gag sequences in 246 out of 324 HIV-1-infected Ghanaians. Phylogeny analysis revealed that 200 (81.3%) individuals were infected with HIV-1 CRF02_AG. Full gag and vif sequences were obtained from 199 and 138, respectively, out of the 200 individuals infected with CRF02_AG and subjected to determination of HLA-associated mutations. The analysis found HLA-associated HIV-1 CRF02_AG non-synonymous polymorphisms at 19 sites; 13 in gag and six in vif, including those that were newly determined. Generation of this data is an important contribution to our understanding of HIV-1 CRF02_AG and host T cell interaction.
UR - http://www.scopus.com/inward/record.url?scp=85075389905&partnerID=8YFLogxK
U2 - 10.7883/yoken.JJID.2019.201
DO - 10.7883/yoken.JJID.2019.201
M3 - Article
C2 - 31257246
AN - SCOPUS:85075389905
SN - 1344-6304
VL - 72
SP - 374
EP - 380
JO - Japanese Journal of Infectious Diseases
JF - Japanese Journal of Infectious Diseases
IS - 6
ER -