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机构地区:[1]北京医科大学人民医院肝病研究所 [2]北京中日友好医院检验科
出 处:《临床肝胆病杂志》1998年第3期153-155,共3页Journal of Clinical Hepatology
摘 要:目的探讨肝癌及肝硬化患者中HGV的感染状态及NS3区部分基因的酶切分析。采用RTPCR技术检测HGVRNA,酶切分析比较中国株与美国GBV-C株两种基因型的酶切位点。结果81例肝癌样品中9例HGVRNA阳性(11.11%),28例肝硬化中,3例HGVRNA阳性(10.7%)。酶切位点分析结果表明,中国HGV感染患者在GBV-C4351位存在TSP509I(AA↓TT)切点,美国和日本发表的11株GBV-C和1株HGV中仅2株存在此切点。结论酶切分析结果提示GBV-C株与中国HGV感染株。To detect the presence of hepatitis G virus infection in patients with hepatocellular carcinoma and liver cirrhosis and analyze the NS3 gene with restrict endounclease.RT PCr technique was used to detect HGV RNA.Positive PCR products were digested with restrict endonuclease to find the existence of certain recognization site.Results:9 samples(11.1%) were HGV RNA positive in 81 patints with hepatocellular carcinoma,and 3(10.7%) were positive in 28 patients with liver cirrhosis.When digested with restrict endonuclease,all Chinese isolates had TSP 509I (AA↓TT) recognization site in nt 4351 (GBVC position),however,only 2 of 12 American and Japanese isolates (11 GBVC isolates and 1 HGV isolate)had this site.Conclusion:The result of restrict endonuclease analysis demonstrated that Chinese HGv isolate and GBVC isolate may belong to different genotype.
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