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克罗地亚丙型肝炎病毒的分子流行病学及对直接作用抗病毒药物的基线耐药性

Molecular Epidemiology and Baseline Resistance of Hepatitis C Virus to Direct Acting Antivirals in Croatia.

作者信息

Simicic Petra, Slovic Anamarija, Radmanic Leona, Vince Adriana, Zidovec Lepej Snjezana

机构信息

Department of Immunological and Molecular Diagnostics, University Hospital for Infectious Diseases, 10000 Zagreb, Croatia.

Centre for Research and Knowledge Transfer in Biotechnology, University of Zagreb, 10000 Zagreb, Croatia.

出版信息

Pathogens. 2022 Jul 19;11(7):808. doi: 10.3390/pathogens11070808.

Abstract

Molecular epidemiology of hepatitis C virus (HCV) is exceptionally complex due to the highly diverse HCV genome. Genetic diversity, transmission dynamics, and epidemic history of the most common HCV genotypes were inferred by population sequencing of the HCV NS3, NS5A, and NS5B region followed by phylogenetic and phylodynamic analysis. The results of this research suggest high overall prevalence of baseline NS3 resistance associate substitutions (RAS) (33.0%), moderate prevalence of NS5A RAS (13.7%), and low prevalence of nucleoside inhibitor NS5B RAS (8.3%). Prevalence of RAS significantly differed according to HCV genotype, with the highest prevalence of baseline resistance to NS3 inhibitors and NS5A inhibitors observed in HCV subtype 1a (68.8%) and subtype 1b (21.3%), respectively. Phylogenetic tree reconstructions showed two distinct clades within the subtype 1a, clade I (62.4%) and clade II (37.6%). NS3 RAS were preferentially associated with clade I. Phylogenetic analysis demonstrated that 27 (9.0%) HCV sequences had a presumed epidemiological link with another sequence and classified into 13 transmission pairs or clusters which were predominantly comprised of subtype 3a viruses and commonly detected among intravenous drug users (IDU). Phylodynamic analyses highlighted an exponential increase in subtype 1a and 3a effective population size in the late 20th century, which is a period associated with an explosive increase in the number of IDU in Croatia.

摘要

由于丙型肝炎病毒(HCV)基因组高度多样,其分子流行病学异常复杂。通过对HCV NS3、NS5A和NS5B区域进行群体测序,随后进行系统发育和系统动力学分析,推断出最常见HCV基因型的遗传多样性、传播动态和流行病史。本研究结果表明,基线NS3耐药相关替代(RAS)的总体患病率较高(33.0%),NS5A RAS的患病率中等(13.7%),核苷类抑制剂NS5B RAS的患病率较低(8.3%)。RAS的患病率因HCV基因型而异,在HCV 1a亚型(68.8%)和1b亚型(21.3%)中分别观察到对NS3抑制剂和NS5A抑制剂的基线耐药率最高。系统发育树重建显示1a亚型内有两个不同的进化枝,进化枝I(62.4%)和进化枝II(37.6%)。NS3 RAS优先与进化枝I相关。系统发育分析表明,27条(9.0%)HCV序列与另一条序列存在推测的流行病学联系,并被分类为13个传播对或簇,这些传播对或簇主要由3a亚型病毒组成,且在静脉吸毒者(IDU)中普遍检测到。系统动力学分析强调了20世纪后期1a亚型和3a亚型有效种群数量呈指数增长,这一时期与克罗地亚IDU数量的爆发性增长有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba6a/9323280/ff80f5c350a4/pathogens-11-00808-g001.jpg

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