首页> 中文期刊> 《现代生物医学进展》 >实时定量RT-PCR对乙型肝炎病毒全长RNA(fRNA)的定量检测

实时定量RT-PCR对乙型肝炎病毒全长RNA(fRNA)的定量检测

         

摘要

Objective:To establish a simple assay for the detection and quantization of full-length RNA (fRNA) terminating at polyadenilation site in sera of chronic hepatitis B (CHB) patients.Methods:fRNA were assayed via TaqMan real-time RT/PCR using anchored oligo-dT primers in sera of 53 treatment-naive CHB patients and 22 HBsAg-negative healthy controls.Results were analyzed by comparation ofHBV DNA with HBcrAg and HBeAg.Results:The fRNA assay had a lower limit of detection and quantization at 2.3 log copies/ml,and a correlation coefficient of 0.99 (P<0.0001).fRNA was detected in 29 of 53 (54.7%) of the CHB patients as compared to non of 22 controls (Specificity).fRNA was detected in all 27 HBeAg-positive and/or high HBV DNA levels CHB patients as compared to 2 of 26 (7.7%) HBeAg-negative and low HBV DNA levels CHB patients (P<0.0001).fRNA levels were higher in HBeAg-positive than in HBeAg-negative samples (5.0± 0.3 vs.2.9± 0.4 log copies/ml,P<0.001).Significant correlation was found between fRNA and HBV DNA/HBcrAg (r=0.905 and 0.881,respectively,P<0.0001).The effective items on fRNA levels,in descending order,were:HBV DNA,HBcrAg by means of Hayashi's quantification method type Ⅰ (Multiple correlation efficient=0.939).Conclusion:The simple real-time RT/PCR for detection and quantization of fRNA was suitable for routine clinical test in assessing HBV replication status the same as HBV DNA and HBeAg in CHB patients.%目的:建立一种简便的定量检测慢性乙型肝炎患者血清中终止于聚腺苷酸化位点的乙型肝炎病毒全长RNA(fRNA)的方法.方法:选取53例未治疗的乙型肝炎患者及22例HBsAg阴性的健康者为研究对象,使用锚定oligo-dT的引物对其血清中fRNA进行实时定量反转录PCR检测,统计分析其与HBV DNA、HBcrAg和HBeAg的相关性.结果:对fRNA进行实时荧光定量RT-PCR检测的下线为2.3 log copies/ml,标准曲线的相关系数为0.99(P<0.0001).53例乙型肝炎患者中,29例(54.7%)可以检测到fRNA,22例正常对照中没有检测到fRNA.27例HBeAg阳性和/或高水平HBV DNA的患者全部检测到fRNA,26例HBeAg阴性并且低水平HBV DNA的乙型肝炎患者中有2例(7.7%)检测到fRNA (P<0.0001).HBeAg阳性患者血清中fNA水平高于HBeAg阴性患者(5.0±0.3 vs.2.9± 0.4 log copies/ml,P<0.001).fRNA与HBV DNA/HBcrAg具有显著相关性(闻.905、0.881,P<0.0001).Hayashi's定量分析法Ⅰ显示fRNA与HBV DNA相关性强于其与HBcrAg的相关性.结论:与HBV DNA和HBeAg一样,fRNA可作为常规检测判断HBV的复制水平并指导用药.

著录项

  • 来源
    《现代生物医学进展》 |2015年第1期|29-32|共4页
  • 作者单位

    第四军医大学唐都医院病理科第四军医大学唐都医院妇产科 陕西西安710038;

    第四军医大学唐都医院病理科第四军医大学唐都医院妇产科 陕西西安710038;

    第四军医大学唐都医院病理科第四军医大学唐都医院妇产科 陕西西安710038;

    第四军医大学唐都医院病理科第四军医大学唐都医院妇产科 陕西西安710038;

    第四军医大学唐都医院病理科第四军医大学唐都医院妇产科 陕西西安710038;

    第四军医大学唐都医院病理科第四军医大学唐都医院妇产科 陕西西安710038;

    第四军医大学唐都医院病理科第四军医大学唐都医院妇产科 陕西西安710038;

    第四军医大学唐都医院病理科第四军医大学唐都医院妇产科 陕西西安710038;

  • 原文格式 PDF
  • 正文语种 chi
  • 中图分类 R512.62;
  • 关键词

    HBV RNA; 实时荧光定量; fRNA; Hayashi's定量法;

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