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首页> 外文期刊>Infection and Drug Resistance >Prevalence of hepatitis C virus-resistant association substitutions to direct-acting antiviral agents in treatment-na?ve hepatitis C genotype 1b-infected patients in western China
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Prevalence of hepatitis C virus-resistant association substitutions to direct-acting antiviral agents in treatment-na?ve hepatitis C genotype 1b-infected patients in western China

机译:在中国西部未经治疗的丙型肝炎基因型1b感染患者中,丙型肝炎病毒抗性联想替代品对直接作用抗病毒药的流行

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摘要

Background: Direct-acting antivirals (DAAs) against hepatitis C virus (HCV) are potent and highly efficacious. However, resistance-associated substitutions (RASs) relevant to DAAs can impair treatment effectiveness even at baseline. Moreover, the prevalence of baseline RASs in HCV genotype 1b-infected patients in western China is still unclear. Materials and methods: Direct sequencing of the HCV NS3, NS5A, and NS5B regions was performed in baseline serum samples of 70 DAAs treatment-na?ve HCV 1b-infected patients in western China. The sequences were analyzed with MEGA version 5.05 software. Evolutionary patterns of RASs and amino-acid covariance patterns in the NS3 , NS5A , and NS5B genes were analyzed by MEGA and Cytoscape (version 3.2.1), respectively. Results: The presence of at least one RAS in the NS3 region (C16S, T54S, Q80R/L, A87T, R117H, S122G, V132I, V170I) was observed in 85.48% (53 of 62) of patients, RASs in the NS5A region (L28M, R30Q, Q54H, P58S/T, Q62H/R, Y93H) were observed in 42.42% (28 of 66) of patients, and RASs in the NS5B region (N142S, A300T, C316N, A338V, S365A, L392I, M414L, I424V, A442T, V499A, S556G) were observed in 100% (44 of 44) of patients. Evolutionary patterns of RASs and amino-acid covariance patterns for the NS3 , NS5A , and NS5B genes are reported. Conclusion: The prevalence of RASs relevant to DAAs detected in the NS3, NS5A, and NS5B regions of HCV 1b from DAA treatment-na?ve patients is high. Therefore, more attention should be paid to RASs associated with DAAs in the upcoming DAA-treatment era in China.
机译:背景:针对丙型肝炎病毒(HCV)的直接作用抗病毒药(DAA)高效且高效。但是,即使在基线时,与DAA相关的耐药相关替代(RAS)也会损害治疗效果。此外,在中国西部HCV基因型1b感染患者中基线RAS的患病率仍不清楚。材料和方法:在中国西部70名接受过DAA治疗的初次感染HCV 1b的患者的基线血清样本中,对HCV NS3,NS5A和NS5B区进行了直接测序。用MEGA 5.05版软件分析序列。分别通过MEGA和Cytoscape(3.2.1版)分析了NS3,NS5A和NS5B基因中RAS的进化模式和氨基酸协方差模式。结果:在85.48%(62名患者中的53名)患者中,在NS3A地区中观察到至少一种RAS(C16S,T54S,Q80R / L,A87T,R117H,S122G,V132I,V170I)存在,在NS5A地区患者中存在RAS。在42.42%(66个中的28个)患者中观察到了(L28M,R30Q,Q54H,P58S / T,Q62H / R,Y93H)和NS5B区(N142S,A300T,C316N,A338V,S365A,L392I,M414L)的RAS ,I424V,A442T,V499A,S556G)在100%(44个中的44个)患者中观察到。报道了NS3,NS5A和NS5B基因的RAS进化模式和氨基酸协方差模式。结论:从未接受过DAA治疗的患者在HCV 1b的NS3,NS5A和NS5B区检测到的与DAA相关的RAS发生率很高。因此,在即将到来的中国DAA治疗时代,应更加重视与DAA相关的RAS。

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