Confirmation of Two Novel HIV-1 CRF01_AE/CRF07_BC Recombinant Forms Among Men Who Have Sex with Men in Hebei, China.

IF 1.5 4区 医学 Q4 IMMUNOLOGY
Yapeng Guan, Jun Wang, Meng Liu, Xinli Lu
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引用次数: 0

Abstract

Acquired immune deficiency syndrome caused by human immunodeficiency virus (HIV) is a serious infectious disease because of its' high genetic variability. Nowadays, homosexual contact has become the most predominant transmission route in Hebei province, China, leading to the emergence of novel HIV-1 recombinant forms. The neighbor-joining (N-J) phylogenetic trees were constructed using MEGA 6.0 in order to identify the subtypes of H22063 and H22144. Recombination breakpoints were identified using online resources jpHMM, RIP 3.0, and Simplot 3.5.1. In this study, we identified two novel HIV-1 unique recombinant forms (URFs) _0107 from three men who have sex with men in Hebei province, including H22063 and H22144. The near full-length genome analysis showed H22063 has seven gene recombination sub-regions, including three subtype CRF07_BC gene fragments inserted into the CRF01_AE backbone. H22144 has nine gene recombination sub-regions, including four subtype CRF07_BC gene fragments inserted into the CRF01_AE backbone. This study confirms the emergence of novel recombinant forms and suggests we should strengthen the monitoring of novel HIV recombinant forms in order to deal with the complex HIV-1 epidemiological trend in Hebei province, China.

河北省男男性行为人群中两种新型HIV-1 CRF01_AE/CRF07_BC重组形式的确认
由人类免疫缺陷病毒(HIV)引起的获得性免疫缺陷综合征是一种具有高度遗传变异性的严重传染病。如今,同性恋接触已成为中国河北省最主要的传播途径,导致新型HIV-1重组形式的出现。利用MEGA 6.0构建相邻连接(N-J)系统发育树,鉴定H22063和H22144亚型。使用在线资源jpHMM、RIP 3.0和Simplot 3.5.1确定重组断点。本研究从河北省三名男男性行为者中鉴定出两种新的HIV-1独特重组形式(URFs) _0107,包括H22063和H22144。近全长基因组分析显示,H22063有7个基因重组亚区,包括3个插入CRF01_AE主链的CRF07_BC基因片段。H22144有9个基因重组亚区,包括插入CRF01_AE主干的4个亚型CRF07_BC基因片段。本研究证实了新型HIV重组病毒的出现,建议加强对新型HIV重组病毒的监测,以应对河北省复杂的HIV-1流行趋势。
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来源期刊
CiteScore
3.10
自引率
6.70%
发文量
201
审稿时长
3-6 weeks
期刊介绍: AIDS Research and Human Retroviruses was the very first AIDS publication in the field over 30 years ago, and today it is still the critical resource advancing research in retroviruses, including AIDS. The Journal provides the broadest coverage from molecular biology to clinical studies and outcomes research, focusing on developments in prevention science, novel therapeutics, and immune-restorative approaches. Cutting-edge papers on the latest progress and research advances through clinical trials and examination of targeted antiretroviral agents lead to improvements in translational medicine for optimal treatment outcomes. AIDS Research and Human Retroviruses coverage includes: HIV cure research HIV prevention science - Vaccine research - Systemic and Topical PreP Molecular and cell biology of HIV and SIV Developments in HIV pathogenesis and comorbidities Molecular biology, immunology, and epidemiology of HTLV Pharmacology of HIV therapy Social and behavioral science Rapid publication of emerging sequence information.
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