HIV-1 Genetic Diversity and High Prevalence of Pretreatment Drug Resistance in Tianjin, China

抗性突变 基因型 病毒学 抗药性 逆转录酶 核苷逆转录酶抑制剂 生物 慢病毒 遗传多样性 医学 人类免疫缺陷病毒(HIV) 基因 聚合酶链反应 遗传学 病毒载量 病毒性疾病 抗逆转录病毒疗法 人口 环境卫生
作者
Rui Zeng,Doudou Ren,Xiaowen Gong,Min Wei,Liying Gao,Aiping Yu,Defa Zhang,Yuqiang Mi,Ping Ma
出处
期刊:AIDS Research and Human Retroviruses [Mary Ann Liebert, Inc.]
卷期号:36 (10): 852-861 被引量:19
标识
DOI:10.1089/aid.2020.0056
摘要

Diversity of genotypes and prevalence of pretreatment drug resistance (PDR) are challenges for the epidemic control and vaccine development of HIV-1. However, little is known about the situation in Tianjin. Blood samples were collected from newly diagnosed, antiretroviral treatment (ART)-naive HIV/AIDS patients from January 2016 to November 2019. The target fragment in the pol gene was sequenced after RNA extraction and gene amplification. The HIV-1 genotype was identified by phylogenetic analysis. Drug resistance was carried out using the Stanford University HIVdb algorithm. A total of 305 pol sequences from 279 non-PDR individuals and 35 PDR individuals were successfully amplified. The most prevalent genotype was CRF01_AE (65.6%, 200/305), followed by CRF07_BC (22.0%, 67/305) and B (3.0%, 9/305). A variety of circulating recombinant forms (CRFs) and unique recombinant forms were found. The overall incidence of PDR was 11.5% (35/305), with 9.8% (30/305) to non-nucleoside reverse transcriptase (RT) inhibitors (NNRTIs). The most frequent mutation pattern against NNRTIs was V179D/E/T (6.9%, 21/305), with M184V (1.0%, 3/305) and K65R (1.0%, 3/305) against nucleoside RT inhibitors (NRTIs). M64L (0.1%, 1/305) was the sole mutation found against protease inhibitors (PIs). Eight variants generated at least low-level resistance to NNRTIs (2.6%, 8/305), which was much higher than that to NRTIs (1.6%, 5/305) and PIs (0/305) (p < .05). Genotypic drug resistance testing before initiating ART in newly diagnosed HIV/AIDS patients may be necessary in Tianjin, China. The non-NNRTI-based regimen may be preferred as initial therapy in Tianjin.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
不想过夏天完成签到,获得积分10
1秒前
zhou发布了新的文献求助10
2秒前
2秒前
SciGPT应助于晨欣采纳,获得10
2秒前
Mizuki完成签到,获得积分10
3秒前
gstaihn完成签到,获得积分10
4秒前
5秒前
6秒前
量子星尘发布了新的文献求助10
9秒前
体贴幻香发布了新的文献求助10
10秒前
he发布了新的文献求助10
10秒前
文艺的猕猴桃关注了科研通微信公众号
11秒前
cai_by完成签到,获得积分10
11秒前
Hello应助Muran采纳,获得10
12秒前
月满西楼完成签到 ,获得积分10
12秒前
思你如初完成签到 ,获得积分10
12秒前
zh_li完成签到,获得积分10
13秒前
13秒前
勤恳天宇完成签到,获得积分20
14秒前
rio完成签到 ,获得积分10
14秒前
Taylor完成签到 ,获得积分10
15秒前
zhou完成签到,获得积分10
15秒前
16秒前
mama发布了新的文献求助10
17秒前
晓晓完成签到,获得积分10
17秒前
拼搏宝莹发布了新的文献求助10
17秒前
18秒前
上官若男应助科研通管家采纳,获得10
18秒前
18秒前
18秒前
18秒前
我是老大应助科研通管家采纳,获得10
18秒前
18秒前
领导范儿应助科研通管家采纳,获得10
18秒前
18秒前
京墨襦完成签到 ,获得积分10
18秒前
老福贵儿应助科研通管家采纳,获得10
18秒前
上官若男应助科研通管家采纳,获得10
18秒前
炎星语完成签到,获得积分10
19秒前
筱璞羲完成签到,获得积分10
20秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Handbook of pharmaceutical excipients, Ninth edition 5000
Aerospace Standards Index - 2026 ASIN2026 3000
Polymorphism and polytypism in crystals 1000
Signals, Systems, and Signal Processing 610
Discrete-Time Signals and Systems 610
T/SNFSOC 0002—2025 独居石精矿碱法冶炼工艺技术标准 600
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 纳米技术 有机化学 物理 生物化学 化学工程 计算机科学 复合材料 内科学 催化作用 光电子学 物理化学 电极 冶金 遗传学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 6044738
求助须知:如何正确求助?哪些是违规求助? 7813092
关于积分的说明 16246129
捐赠科研通 5190459
什么是DOI,文献DOI怎么找? 2777385
邀请新用户注册赠送积分活动 1760617
关于科研通互助平台的介绍 1643767