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在人类免疫缺陷病毒合并感染和高效抗逆转录病毒治疗的情况下,追踪研究了 4 到 11 年的丙型肝炎病毒 1a 基因型的超变区包膜编码区的种内和种间变异性。

Inter and intra-host variability of hepatitis C virus genotype 1a hypervariable envelope coding domains followed for a 4-11 year of human immunodeficiency virus coinfection and highly active antiretroviral therapy.

机构信息

Instituto de Investigaciones Biomédicas en Retrovirus y Sida (INBIRS), Universidad de Buenos Aires, Argentina; Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Argentina.

Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Argentina; Laboratorio de Virología y Genética Molecular, Facultad de Ciencias Naturales sede Trelew, Universidad Nacional de la Patagonia San Juan Bosco, Chubut, Argentina.

出版信息

Virology. 2014 Dec;471-473:19-28. doi: 10.1016/j.virol.2014.09.016. Epub 2014 Oct 20.

Abstract

The evolution of hepatitis C virus (HCV) quasispecies in patients with HIV-1 coinfection is not fully understood. The HCV-1a quasispecies heterogeneity was analyzed at inter and intra-host levels along 7.6 years in 21 coinfected patients that showed different virological and immunological responses to highly active antiretroviral therapy (HAART). Two to nine serial samples were subjected to direct and clonal sequence analyses of the envelope glycoprotein 2 (E2) gene. E2-based phylogenies, intra-host HCV evolution and evolutionary rates, as well as dynamics of the quasispecies heterogeneity parameters were evaluated. Bayesian coalescent phylogenies indicated complex evolutionary histories, revealing some viral lineages that persisted along the follow up and others that were detectable at a single or some sampling times, suggesting the occurrence of emergence-extinction cycles. HCV quasispecies underwent very rapid evolution in HAART-treated patients (~3.1 × 10(-2) sub/site/year) following the recovery of the host immunocompetence irrespectively of the virological response to HAART.

摘要

丙型肝炎病毒(HCV)准种在 HIV-1 合并感染患者中的演变尚不完全清楚。对 21 例接受高效抗逆转录病毒治疗(HAART)的合并感染患者进行了 HCV-1a 准种异质性的分析,这些患者在病毒学和免疫学方面对 HAART 表现出不同的反应。对 2 到 9 个连续样本进行了包膜糖蛋白 2(E2)基因的直接和克隆序列分析。对 E2 基的系统发生树、宿主内 HCV 进化和进化率以及准种异质性参数的动态进行了评估。贝叶斯合并系统发生树表明存在复杂的进化历史,揭示了一些在随访期间持续存在的病毒谱系,以及在单个或某些采样时间检测到的其他病毒谱系,这表明存在出现-灭绝循环。在宿主免疫功能恢复后,HAART 治疗的患者中的 HCV 准种经历了非常快速的进化(~3.1×10^(-2) 取代/位点/年),而与对 HAART 的病毒学反应无关。

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