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首页> 外文期刊>Journal of Clinical Microbiology >Discrimination of hepatitis C virus in liver tissues from different patients with hepatocellular carcinomas by direct nucleotide sequencing of amplified cDNA of the viral genome.
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Discrimination of hepatitis C virus in liver tissues from different patients with hepatocellular carcinomas by direct nucleotide sequencing of amplified cDNA of the viral genome.

机译:通过对病毒基因组cDNA进行直接核苷酸测序来区分不同肝癌患者肝组织中的丙型肝炎病毒。

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We investigated the presence of the hepatitis C virus (HCV) genome in liver tissues of eight different patients with hepatocellular carcinoma by using the reverse transcriptase polymerase chain reaction (PCR) method. RNA was extracted separately from cancerous and peripheral noncancerous portions of the liver tissues of each patient. For reverse transcriptase PCR, we used sets of primers derived either from nonstructural region 3 (the NS3 region) or from the nucleocapsid-envelope (C/E) region of the HCV genome. The nucleotide sequences of the amplimers were directly determined without subcloning. Of 16 samples tested, cDNA of the HCV genome was detected in 2 cancerous tissues and in 4 noncancerous tissues by either pair of primers. Nucleotide sequences of HCV cDNA fragments amplified from cancerous and peripheral noncancerous tissues from the same patients were identical. However, 4.4 to 6.3% and 7.5 to 11.3% sequence variation was observed in NS3 and C/E regions, respectively, among cDNA fragments from different patients. The result indicated that the HCV genome detected in a given patient is distinguishable from that in others by a simple direct nucleotide sequencing of the reverse transcriptase PCR products.
机译:我们使用逆转录酶聚合酶链反应(PCR)方法研究了八名不同肝细胞癌患者肝组织中丙型肝炎病毒(HCV)基因组的存在。从每个患者肝组织的癌性和外周性非癌性部分分别提取RNA。对于逆转录酶PCR,我们使用了衍生自HCV基因组的非结构区3(NS3区)或核衣壳(C / E)区的引物组。无需亚克隆即可直接确定扩增子的核苷酸序列。在测试的16个样品中,通过任一对引物在2个癌性组织和4个非癌性组织中检测到HCV基因组的cDNA。从同一患者的癌组织和周围非癌组织中扩增出的HCV cDNA片段的核苷酸序列相同。然而,在来自不同患者的cDNA片段中,在NS3和C / E区域分别观察到4.4至6.3%和7.5至11.3%的序列变异。结果表明,通过逆转录酶PCR产物的简单直接核苷酸测序,在给定患者中检测到的HCV基因组可与其他患者区分开。

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