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中国广东一种新型HIV-1流行重组型(CRF156_0755)的分子遗传学特征分析

Molecular genetic characterization analysis of a novel HIV-1 circulating recombinant form (CRF156_0755) in Guangdong, China.

作者信息

Lin Yaqing, Lan Xianglong, Xin Ruolei, Ling Xuemei, Xiao Mingfeng, Li Feng, Hu Fengyu, Li Linghua, Lan Yun

机构信息

Institute of Infectious Diseases, Guangzhou Eighth People's Hospital, Guangzhou Medical University, Guangzhou, China.

Institute of AIDS/STD Prevention and Control, Beijing Center for Disease Prevention and Control, Beijing, China.

出版信息

Front Microbiol. 2024 May 3;15:1387720. doi: 10.3389/fmicb.2024.1387720. eCollection 2024.

Abstract

INTRODUCTION

The characteristic of human immunodeficiency virus type 1 (HIV-1) is its susceptibility to erroneous replication and recombination, which plays a crucial role in the diverse and dynamic variation of HIV-1. The spread of different subtypes in the same population often leads to the emergence of circulating recombination forms (CRFs). At present, the main recombinant subtypes of HIV-1 in China are CRF07_BC, CRF01_AE, CRF08_BC and B' subtypes, while CRF55_01B has become the fifth major epidemic strain in China after rapid growth in recent years since it was first reported in 2013. In this study, we obtained five nearly full-length genomes (NFLGs) and one half-length genome from five different cities in Guangdong. Here, we focused on analyzing their characteristics, parental origin and drug resistance.

METHODS

Plasma samples were collected from six HIV-1 infected patients in Guangdong Province who had no epidemiological association with each other. The NFLGs of HIV-1 were amplified in two overlapping segments by the near-terminal dilution method. The positive products were sequenced directly to obtain genomic sequences. The recombinant patterns and breakpoints of the NFLGs were determined using the Simplot software and confirmed by the maximum likelihood trees for segments using the IQ-TREE and BEAST software. The genotypic resistance profiles of the protease reverse transcriptase and integrase were resolved by the Stanford HIV drug resistance database.

RESULTS

The six genomes shared highly similar recombinant pattern, with the CRF55_01B backbone substituted by CRF07_BC segments, therefore assigned as CRF156_0755. The evolutionary analysis of the segments showed that CRF07_BC segments were not clustered with the Chinese MSM variants in the CRF07_BC lineage. All the five NFLGs were identified with the non-nucleoside reverse-transcription inhibitors (NNRTIs) resistance mutation V179E.

DISCUSSION

With the accumulation and evolution of recombination between CRF55_01B and CRF 07_BC, the prevalence of more recombinant strains of CRF55_01B and CRF 07_BC may occur. Therefore, it is necessary to strengthen the identification and monitoring of the recombination of CRF55_01B and CRF 07_BC.

摘要

引言

1型人类免疫缺陷病毒(HIV-1)的特点是易于错误复制和重组,这在HIV-1的多样动态变异中起关键作用。不同亚型在同一人群中的传播常导致循环重组型(CRF)的出现。目前,中国HIV-1的主要重组亚型为CRF07_BC、CRF01_AE、CRF08_BC和B'亚型,而CRF55_01B自2013年首次报道以来,近年来快速增长,已成为中国第五大主要流行毒株。在本研究中,我们从广东五个不同城市获得了五个近全长基因组(NFLG)和一个半长基因组。在此,我们着重分析它们的特征、亲本来源和耐药性。

方法

从广东省六名彼此无流行病学关联的HIV-1感染患者中采集血浆样本。采用近末端稀释法在两个重叠片段中扩增HIV-1的NFLG。对阳性产物直接测序以获得基因组序列。使用Simplot软件确定NFLG的重组模式和断点,并通过IQ-TREE和BEAST软件构建的片段最大似然树进行确认。通过斯坦福HIV耐药数据库解析蛋白酶、逆转录酶和整合酶的基因型耐药谱。

结果

这六个基因组具有高度相似的重组模式,CRF55_01B主干被CRF07_BC片段取代,因此被归类为CRF156_0755。片段的进化分析表明,CRF07_BC片段在CRF07_BC谱系中未与中国男男性行为者(MSM)变异株聚类。所有五个NFLG均鉴定出非核苷类逆转录酶抑制剂(NNRTI)耐药突变V179E。

讨论

随着CRF55_01B与CRF07_BC之间重组的积累和进化,可能会出现更多CRF55_01B与CRF07_BC的重组毒株。因此,有必要加强对CRF55_01B与CRF07_BC重组的鉴定和监测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7862/11099239/af3af85b21a5/fmicb-15-1387720-g001.jpg

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