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逆转录套式聚合酶链反应检测庚型肝炎病毒

Reverse nested polymerase chain reaction for the detection of hepatitis G virus RNA

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【作者】 常锦红魏来陶其敏杜绍财王豪孙焱

【Author】 Chang Jinhong, Wei Lai, Tao Qimin, et al. Hepatology Institute, Beijing Medical University, Beijing 100044

【机构】 北京医科大学人民医院肝病研究所

【摘要】 目的建立敏感、特异的逆转录套式聚合酶链反应(RT-nested-PCR)方法,以检测中国人庚型肝炎病毒(HGV)感染。方法根据中国人感染HGV者NS5区部分核苷酸序列分析结果,设计套式PCR引物,用于HGVRNA的检测,并与用国外报道引物所作的一次PCR和套式PCR检测结果进行比较。结果共检测标本133份。以国外报道引物作一次PCR和套式PCR检出率分别为8.3%和11.3%,作者建立的套式PCR检出率为18.0%,对部分PCR产物进行序列分析证实为HGV特异性基因。结论建立的方法可在中国人群中显著提高HGVRNA检出率。

【Abstract】 Objective To develop a sensitive and specific reverse nested polymerase chain reaction(RT nested PCR)method for the detection of hepatitis G virus (HGV) in Chinese patients. Methods A set of nested PCR primers were designed according to the sequence analysis result of partial NS5 gene of HGV in Chinese patients. Using this set of primers, a RT nested PCR method was developed to detect HGV infection in the Chinese, and its result was compared with one stage PCR and nested PCR, whose primers were designed according to sequences from abroad. Results 133 samples were detected. The positive rate in one stage PCR, nested PCR and our newly developed nested PCR was 8.3%, 11.3% and 18.0% respectively. The specificity of the PCR product was verified by sequence analysis. Conclusion Our developed RT nested PCR method markedly increased the positive rate of HGV RNA among Chinese patients.

  • 【文献出处】 中华医学检验杂志 ,Chinese Journal of Laboratory Medicine , 编辑部邮箱 ,1997年03期
  • 【分类号】Q78
  • 【被引频次】4
  • 【下载频次】17
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