Liang Shan, Liu Zhiyang, Wang Shaoli, Liu Jing, Shi Ling, Mao Wei, Liu Cunxu, Wan Jianhua, Zhu Lili, Huang Mei, Liu Yu, Wang Jingxing, Ness Paul, Shan Hua, Zeng Peibin, He Miao
Institute of Blood Transfusion, Chinese Academy of Medical Sciences, Chengdu, China.
Sichuan Blood Safety and Blood Substitute International Science and Technology Cooperation Base, Chengdu, China.
PLoS One. 2020 Dec 21;15(12):e0243650. doi: 10.1371/journal.pone.0243650. eCollection 2020.
Human immunodeficiency virus-1 (HIV-1) exhibits high diversity and complexity in China, challenging the disease surveillance and antiretroviral therapy. Between July 1, 2014 and January 30, 2017, we investigated the profiles of HIV-1 infection stages, genotype distribution and drug resistance mutations (DRMs) using plasma samples from HIV Western blot (WB) confirmed blood donors from five Chinese blood centers (Chongqing, Guangxi, Luoyang, Mianyang, and Urumqi). HIV pol regions consisted of whole protease and partial reverse transcriptase were genotyped and analyzed for DRMs. Lag-Avidity testing was performed to identify the infection stages. Of the 356 HIV-1 WB positive samples tested by Lag-avidity assay, 19.1% (68/356) were recent infections. Genotyping on 356 amplified sequences presented the subtype distributions as following: CRF07_BC (65.7%), CRF08_BC (7.3%), CRF01_AE (19.1%), B (4.2%), CRF55_01B (3.1%), CRF59_01B (0.3%) and CRF68_01B (0.3%). No significant difference in genotype distribution was observed between recent and long-term infections. 48 DRMs were identified from 43 samples, indicating a drug resistance prevalence of 12.1% (43/356), which include seven protease inhibitors (PIs) accessory DRMs (Q58E, L23I and I84M), two PIs major DRMs (M46I, M46L), seven nucleoside RT inhibitors DRMs (D67N, K70Q, K219R and M184L), and 32 non-nucleoside RT inhibitors DRMs (K103N, V179E, K238N, V179D, E138G, G190E, A98G, Y188D and E138A). In addition, we had also identified CRFs from the 01B subtype including CRF55_01B (3.1%), CRF59_01B (0.3%) and CRF68_01B (0.3%). As an important part of the continuous monitoring of HIV-1 circulating strains among blood donors, our findings were expected to contribute to the comprehensive AIDS control and development of proper diagnostics for HIV-1 in China.
人类免疫缺陷病毒1型(HIV-1)在中国呈现出高度的多样性和复杂性,这对疾病监测和抗逆转录病毒治疗构成了挑战。在2014年7月1日至2017年1月30日期间,我们使用来自中国五个血液中心(重庆、广西、洛阳、绵阳和乌鲁木齐)经HIV免疫印迹法(WB)确认的献血者的血浆样本,调查了HIV-1感染阶段、基因型分布和耐药突变(DRMs)情况。对HIV pol区域(包括整个蛋白酶和部分逆转录酶)进行基因分型并分析DRMs。进行迟滞亲和力检测以确定感染阶段。在通过迟滞亲和力检测的356份HIV-1 WB阳性样本中,19.1%(68/356)为近期感染。对356条扩增序列进行基因分型,呈现出如下亚型分布:CRF07_BC(65.7%)、CRF08_BC(7.3%)、CRF01_AE(19.1%)、B(4.2%)、CRF55_01B(3.1%)、CRF59_01B(0.3%)和CRF68_01B(0.3%)。近期感染和长期感染之间在基因型分布上未观察到显著差异。从43份样本中鉴定出48个DRMs,表明耐药率为12.1%(43/356),其中包括7个蛋白酶抑制剂(PIs)辅助DRMs(Q58E、L23I和I84M)、2个PIs主要DRMs(M46I、M46L)、7个核苷类逆转录酶抑制剂DRMs(D67N、K70Q、K219R和M184L)以及32个非核苷类逆转录酶抑制剂DRMs(K103N、V179E、K238N、V179D、E138G、G190E、A98G、Y188D和E138A)。此外,我们还从01B亚型中鉴定出了CRFs,包括CRF55_01B(3.1%)、CRF59_01B(0.3%)和CRF68_01B(0.3%)。作为对献血者中HIV-1流行毒株持续监测的重要组成部分,我们的研究结果有望为中国全面控制艾滋病以及开发合适的HIV-1诊断方法做出贡献。