中国北京两个新型独特重组体(CRF01_AE/CRF07_BC)的近全长基因组特征。

IF 1.5 4区 医学 Q4 IMMUNOLOGY
AIDS research and human retroviruses Pub Date : 2024-10-01 Epub Date: 2024-04-16 DOI:10.1089/AID.2023.0149
Chunlin Lan, Bo Zhu, Hailong Zhuo, Yuting Shi, Zixuan Sun, Lixuan Zhang, Lei Jia, Hanping Li, Yongjian Liu, Xiaolin Wang, Jingyun Li, Bohan Zhang, Jingwan Han, Junjun Jiang, Lin Li
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引用次数: 0

摘要

随着HIV-1 CRF01_AE和CRF07_BC亚型在中国的流行,多种亚型在HIV-1阳性人群中的共同流行可能导致人群的双重感染或超级感染,从而导致HIV-1病毒独特重组型(URF)的出现。本研究发现了两个第二代独特重组株 BI0114 和 BI0116,并获得了它们的近全长基因组序列;重组分析表明,这两个序列都是 URF_0107 的同工型,它们是由 CRF01_AE 和 CRF07_BC 重组形成的第二代独特重组株,同工型分别为 CRF01_AE 和 CRF0107_BC。新型CRF01_AE/CRF07_BC重组株的不断出现,表明HIV-1的流行和防控形势错综复杂,相关卫生部门亟需建立应对毒株重组模式变化的挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Near Full-Length Genome Characterization of Two Novel Unique Recombinants (CRF01_AE/CRF07_BC) in Beijing, China.

With the prevalence of human immunodeficiency virus type 1 (HIV-1) CRF01_AE and CRF07_BC subtypes in China, the co-circulation of multiple subtypes in the HIV-1-positive population may result in dual infection or superinfection in the population, leading to the emergence of unique recombinant forms (URFs) of the HIV-1 virus. In this study, two second-generation unique recombinant strains, BI0114 and BI0116, were identified, and their near full-length genome sequences were obtained. Recombination analysis showed that both sequences were isoforms of URF_0107, and they were second-generation unique recombinant strains formed by the recombination of CRF01_AE and CRF07_BC, with the isoforms being CRF01_AE and CRF0107_BC, respectively. The continued emergence of novel CRF01_AE/CRF07_BC recombinant strains suggests that the epidemiological, preventive, and control situation of HIV-1 is complex and that the relevant health authorities urgently need to establish responses to the challenges posed by changes in the pattern of strain recombination.

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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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