首页> 外文期刊>Indian Journal of Biotechnology >Genotype analysis and assessment of antigenic sensitivity for recombinant HCV proteins by indigenous SIBA for detection of Hepatitis C Virus infection: A comparison with 3(rd) EIA and RT-PCR
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Genotype analysis and assessment of antigenic sensitivity for recombinant HCV proteins by indigenous SIBA for detection of Hepatitis C Virus infection: A comparison with 3(rd) EIA and RT-PCR

机译:基因型分析和本地SIBA对重组HCV蛋白抗原敏感性的评估,以检测丙型肝炎病毒感染:与3(rd)EIA和RT-PCR的比较

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摘要

The first serological testing for the detection of anti-HCV antibodies using recombinant antigens was introduced in 1991. Since then many developments have taken place and at present third generation ELISA kits are being used most widely and globally. Detection of anti-HCV does not distinguish past from present infections and in diagnostic virology particularly ELISA's, a positive HCV test result may be non-specific and therefore has to be crosschecked by another test of different principle for which Immunoblots were initially developed. Patients with liver disease attending the inpatient and outpatient wards of the CLRD (Center for Liver Research and Diagnostics) between Aug 2004 and Feb 2007 were screened for HCV by using 3(rd) generation ELISA, HCV blot, and RT-PCR. Genotyping was done for all the positive samples. Out of 531 samples tested, 211 samples showed identical results as reactive by ELISA, HCV blot and RT-PCR. Out of the 214 genotype samples, genotype 1a was found to be prevalent by 52.33% (n = 112), followed by others. RNA based detection by RT-PCR remains the reliable method of HCV diagnosis, however, where there are no facilities for the PCR to be performed particularly in the small to medium laboratory and diagnostic centers, HCV blot could be done as a supplemental assay.
机译:1991年首次进行了使用重组抗原检测抗HCV抗体的血清学测试。此后进行了许多开发,目前第三代ELISA试剂盒正在最广泛和全球范围内使用。抗HCV的检测不能与过去的感染区别开来,在诊断病毒学(尤其是ELISA)中,HCV阳性检测结果可能是非特异性的,因此必须通过另一项针对免疫印迹最初开发的原理的检测进行交叉检查。使用第三代ELISA,HCV印迹和RT-PCR对2004年8月至2007年2月间在CLRD(肝脏研究和诊断中心)住院和门诊就诊的肝病患者进行HCV筛查。对所有阳性样品进行基因分型。在531个测试样品中,有211个样品显示出与ELISA,HCV印迹和RT-PCR反应相同的结果。在214个基因型样本中,发现基因型1a的流行率为52.33%(n = 112),其次是其他。通过RT-PCR进行基于RNA的检测仍然是HCV诊断的可靠方法,但是,如果没有进行PCR的设施,特别是在中小型实验室和诊断中心,可以将HCV印迹作为补充测定。

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