Characterization of an Invisible HIV-1 Circulating Recombinant Form (CRF149_01B) in China.

IF 1.5 4区 医学 Q4 IMMUNOLOGY
Min Chen, Huichao Chen, Jie Dai, Lijuan Dong, Yanling Ma, Manhong Jia
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引用次数: 0

Abstract

In this study, by analyzing the available near full-length genome (NFLG) sequences of CRF55_01B, it was found that two of the NFLG sequences could not be clustered with other NFLG sequences. Recombination analysis and phylogenetic analysis suggested that these two NFLG sequences arose by recombination with subtype B based on CRF55_01B, rather than by recombination directly derived from CRF01_AE and subtype B. In addition, two other HIV-1 partial gene fragments found in the database shared the same characteristics as these two NFLG sequences in the key recombination region. These sequences may therefore represent a previously unrecognized circulating recombinant form (CRF), which has been named CRF149_01B. Evolutionary analyses suggested that CRF149_01B emerged between approximately 2005 and 2007. The discovery of CRF149_01B highlights the complexity of HIV recombinant evolution and advances the refinement of the HIV genotyping system. A deeper understanding of HIV-1 genetics will facilitate molecular tracing and provide a basis for studying the biological properties of HIV.

中国HIV-1隐形循环重组形式(CRF149_01B)的鉴定
本研究通过对CRF55_01B现有的近全长基因组(near full-length genome, NFLG)序列进行分析,发现其中两个序列不能与其他NFLG序列聚类。重组分析和系统发育分析表明,这两个NFLG序列是基于CRF55_01B与B亚型重组而产生的,而不是直接从CRF01_AE和B亚型重组而来。此外,数据库中另外两个HIV-1部分基因片段在关键重组区域与这两个NFLG序列具有相同的特征。因此,这些序列可能代表一种以前未被识别的循环重组形式(CRF),已被命名为CRF149_01B。进化分析表明,CRF149_01B大约在2005年至2007年间出现。CRF149_01B的发现凸显了HIV重组进化的复杂性,并推动了HIV基因分型系统的完善。对HIV-1基因的深入了解将有助于分子示踪,为研究HIV的生物学特性提供基础。
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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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