Molecular epidemiology of HIV-1 subtypes in southern China

被引:9
|
作者
Laeyendecker, O
Zhang, GW
Quinn, TC
Garten, R
Ray, SC
Lai, SG
Liu, W
Chen, X
Yu, XF
机构
[1] NIAID, Immunoregulat Lab, NIH, Bethesda, MD 20892 USA
[2] Johns Hopkins Univ, Sch Hyg & Publ Hlth, Dept Mol & Microbiol & Immunol, Baltimore, MD USA
[3] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD USA
[4] Johns Hopkins Univ, Sch Hyg & Publ Hlth, Dept Epidemiol, Baltimore, MD USA
[5] Guangxi Hlth & Anti Epidem Ctr, Guangxi, Peoples R China
关键词
HIV-1; CRF01_AE; CRF08_BC; China;
D O I
暂无
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The driving forces of the HIV-1 epidemic in Guangxi, China were assessed by investigating virologic and epidemiologic data from a cohort of longitudinally followed injection drug users (IDUs) in Binyang and Pingxiang, major urban areas along 2 separate drug routes in the province. Sera and interview data were obtained in September and October of 2000. Sequence analysis of HIV-1 was per-formed on the gag-pol region (HXB2 nt 1850-3005) and C2 to V4 env (HXB2 nt 6704-7626). Sequence data demonstrated that 88% of the infections in Pingxiang were CRF01_AE, whereas 96% in Binyang were CRF08_BC. Three recently infected subjects in Pingxiang were infected with CRFOS_BC, and 1 chronically infected subject had evidence of a recombinant virus. Intersubject distances were statistically greater for CRF01_AE-infected subjects than CRF08_BC-infected subjects for all regions except V4. The epidemic in Binyang is similar to previously described IDU-based epidemics, with a strong founder effect with little variation in V3. The epidemic in Pingxiang may have had multiple introductions of the CRF01_AE epidemic into the city and greater spread through sexual transmission, resulting in greater variation in V3 than typically seen in purely parenterally based epidemics.
引用
收藏
页码:356 / 362
页数:7
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