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基因1b型慢性丙型肝炎患者DAAs天然耐药突变分析

Naturally occurring resistance mutations to direct-acting antiviral agents in chronic HCV genotype 1b infection patients

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【作者】 傅涓涓孔玮晶蒋栋魏来潘修成

【Author】 FU Juanjuan;KONG Weijing;JIANG Dong;WEI Lai;PAN Xiucheng;Department of Infectious Diseases,The Affiliated Hosipital of Xuzhou Medical College;Peking University People’s Hospital,Peking University Hepatology Institute;

【通讯作者】 魏来;潘修成;

【机构】 徐州医学院附属医院感染性疾病科北京大学人民医院北京大学人民医院肝病研究所

【摘要】 目的 探讨未经抗病毒治疗的基因1b型慢性丙型肝炎患者天然耐药突变情况。方法 应用RTPCR法扩增丙型肝炎病毒(HCV) NS3及NS5B部分片段序列,用克隆测序方法进行核苷酸序列测定。在氨基酸水平与已有报道的蛋白酶抑制剂耐药突变位点(V36、T54、V55、Q80、R155、A156、D168和V170)和聚合酶抑制剂耐药突变位点(S282、C316、S365、M414、L419、M423和Y448)进行比较。结果 9例患者中3例存在直接抗病毒药物(DAAs)耐药突变,在3例检测到蛋白酶抑制剂耐药突变的患者中2例为T54S突变,1例为A156T突变,存在A156T突变的患者中同时检测到聚合酶抑制剂耐药突变M414L。结论 中国DAAs初治患者中天然存在着蛋白酶抑制剂耐药突变T54S、A156T和聚合酶抑制剂耐药突变M414L。

【Abstract】 Objective Investigate the naturally occurring resistance mutations to HCV protease and polymerase inhibitors in HCV genotype 1b-infected patients who had not previously treated with direct-acting antiviral agents(DAAs).Methods Viral sequences were analyzed in nine patients with chronic HCV genotype 1b infection.Part of the NS3 and NS5B sequences were amplified by reverse transcription(RT)-PCR followed by cloned and sequenced.The sequences were compared with the resistance mutations to HCV protease and polymerase inhibitors.The drug-resistant mutations sites examined here included eight NS3/4A protease inhibitors resistant sites(V36,T54,V55,Q80,R155,A156,D168,and V170),and seven NS5B polymerase inhibitors resistant sites(S282,C316,S365,M414,L419,M423,and Y448).Results Three subjects carryied the DAAs resistance mutations.These three subjects were all detected protease inhibitors resistance mutations.Of the three subjects,two had the T54S substitution,one had the A156T substitution.The subject carrying the A156T mutation were detected polymerase inhibitors resistance mutation M414L.Conclusion Protease inhibitors-resistant mutations T54S,A156T and polymerase inhibitors-resistant mutation M414L were detected in DAAs treatment-na?ve patients in China.

【基金】 国家“十一五”科技重大专项资助项目(2008ZX10002-013)
  • 【文献出处】 徐州医学院学报 ,Acta Academiae Medicinae Xuzhou , 编辑部邮箱 ,2012年09期
  • 【分类号】R512.63
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