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丙型肝炎病毒1b型NS5 A区基因结构变异与α干扰?…
引用本文:段学章,朱传琳.丙型肝炎病毒1b型NS5 A区基因结构变异与α干扰?…[J].中华实验和临床病毒学杂志,1999,13(4):368-370.
作者姓名:段学章  朱传琳
作者单位:中国人民解放军第302医院
摘    要:目的 观察丙型肝炎患者丙型肝炎病毒(HCV)1b型基因组部分NS5 A区核苷酸,氨基酸的变异情况并探讨其与α干扰素疗效的相关性。方法 患者干扰素治疗前,中,后留血标本,用聚合酶链反应(PCR)扩增HCV病毒NS5 A区部分基因片段并用直接测序法测序。与HCV-J株及HCV-河北株(HCV-HB)比较核苷酸及氨基酸序列的同源性,根据α干扰素疗效分析HCV1b是否存在干扰素敏感决定区。

关 键 词:丙型  肝炎病毒  病毒基因  序列分析  干扰素α

Analysis of genome character and amino acid residues 2 209 to 2 248 of NS5 A region of hepatitis C virus in relation to the response to interferon therapy
DUAN Xuezhang,ZHU Chuanlin,CHENG Yun,et al..Analysis of genome character and amino acid residues 2 209 to 2 248 of NS5 A region of hepatitis C virus in relation to the response to interferon therapy[J].Chinese Journal of Experimental and Clinical Virology,1999,13(4):368-370.
Authors:DUAN Xuezhang  ZHU Chuanlin  CHENG Yun  
Institution:Department of Immunology, 302 Hospital of PLA, Beijing 100039.
Abstract:OBJECTIVE: To observe nucleotide sequence variations and amino acid residues 2,209 to 2,248 of the NS5 A region of hepatitis C virus in relation to interferon therapy in Chinese patients infected with HCV genotype 1b. METHODS: We collected sera from 22 patients infected with HCV genotype 1b, performed nested RT-PCR using extracted serum RNA from sera, amplified NS5 A region 2,209 to 2,248 and sequenced the PCR product directly. The deduced amino acid sequences were compared with the corresponding region of the HCV-J prototype strain. RESULTS: Only 4 isolates were intermediate type, and no mutant type was found. In 18 patients treated with IFN-alpha, only 4 were HCV RNA negative at present, No correlation was found between amino acid mutation and IFN response. CONCLUSION: Variations in the NS5 A region between amino acid residues 2,209 to 2,248 failed to predict IFN response in Chinese patients infected with HCV genotype 1b. IFN may accelerate nucleotide variation but has little influence on amino acid variations.
Keywords:Hepatients C virus    Gene  viral    Sequence analysis      Interferon  alpha  
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