HIV-1 subtype diversity and phylogenetic insight into non-B subtype transmission in Slovenia, 1989-2013.

IF 0.6 Q4 DERMATOLOGY Acta Dermatovenerologica Alpina Pannonica et Adriatica Pub Date : 2023-09-01
Jana Mlakar, Maja M Lunar, Ana B Abecasis, Anne-Mieke Vandamme, Janez Tomažič, Tomaž D Vovko, Blaž Pečavar, Gabriele Turel, Mario Poljak
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Abstract

Introduction: Disease progression, drug resistance mutations, and treatment strategies may vary by HIV-1 subtype. This study determined HIV-1 subtypes circulating in Slovenia, a Central European country with an HIV-1 epidemic driven by men who have sex with men, focusing on molecular epidemiology of non-B subtypes.

Methods: A total of 367 HIV-1 sequences were included. Subtype was assigned by employing eight different HIV subtyping tools coupled with maximum likelihood phylogenetic analyses.

Results: The subtyping tools COMET, jpHMM, and REGA 3.0 exhibited the best performance on the dataset studied. Phylogenetic analyses showed a 14.7% prevalence of non-B subtypes, with subtype A detected most frequently (4.9%), followed by CRF02_AG (2.4%), subtype C (1.1%), subtypes D, G, and CRF01_AE (0.8% each), and subtypes F and CRF22_01A1 (0.3% each). A subtype could not be assigned to 12 sequences (3.3%), indicating potential unique recombinant forms. Non-B subtypes were significantly associated with a heterosexual route of transmission and infection acquired in Eastern Europe, Africa, or Asia.

Conclusion: In a country where subtype B is predominant, non-B subtypes were observed in one out of seven patients, a non-negligible proportion, which underlines the importance of systematic surveillance of HIV subtype diversity and the corresponding molecular epidemiology.

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1989-2013年斯洛文尼亚HIV-1亚型多样性和对非B亚型传播的系统发育洞察。
引言:疾病进展、耐药性突变和治疗策略可能因HIV-1亚型而异。这项研究确定了在斯洛文尼亚流行的HIV-1亚型,斯洛文尼亚是一个由男性性行为引起的HIV-1流行的中欧国家,重点关注非B亚型的分子流行病学。方法:共纳入367个HIV-1序列。通过使用八种不同的HIV亚型划分工具,结合最大似然系统发育分析,进行亚型划分。结果:分型工具COMET、jpHMM和REGA 3.0在所研究的数据集上表现出最佳性能。系统发育分析显示,非B亚型的患病率为14.7%,其中a亚型检测频率最高(4.9%),其次是CRF02_AG(2.4%)、C亚型(1.1%)、D、G和CRF01_AE亚型(各0.8%),以及F和CRF22_01A1亚型(分别0.3%)。一个亚型不能被分配到12个序列(3.3%),这表明潜在的独特重组形式。非B亚型与东欧、非洲或亚洲获得的异性传播和感染途径显著相关,它强调了系统监测艾滋病毒亚型多样性和相应的分子流行病学的重要性。
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CiteScore
1.70
自引率
8.30%
发文量
38
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