首页 | 本学科首页   官方微博 | 高级检索  
     检索      

反向线性探针杂交技术检测慢性乙型肝炎病毒拉米夫定耐药研究
引用本文:赖国旗,张文露,胡源,唐红,张磊,谢素兰,潘玥,魏立雯,黄爱龙.反向线性探针杂交技术检测慢性乙型肝炎病毒拉米夫定耐药研究[J].西南师范大学学报(自然科学版),2012,37(3):113-119.
作者姓名:赖国旗  张文露  胡源  唐红  张磊  谢素兰  潘玥  魏立雯  黄爱龙
作者单位:1. 重庆医科大学感染性疾病分子生物学教育部重点实验室,重庆400016;重庆医科大学实验动物中心,重庆400016
2. 重庆医科大学感染性疾病分子生物学教育部重点实验室,重庆,400016
3. 重庆医科大学实验动物中心,重庆,400016
基金项目:“863”课题(Grant No.2008AA02Z424);重庆市教委课题(Grant No KJ100309)
摘    要:目的:建立起简单、快速、灵敏、准确的慢性乙型肝炎病毒拉米夫定耐药位点的反向线性探针(reverse line probe,RLP)检测方法.方法:根据HBV野生及耐药基因序列设计通用探针、3'、5'对称加有poly-C的特异性探针和5'标记生物素的扩增引物.将探针线性固定在硝酸纤维膜上,使HBV PCR扩增产物与探针进行杂交.通过优化杂交条件,建立RLP检测方法.利用该方法对重庆地区86个慢性乙肝病人进行检测,同时与直接测序结果比较.结果:半巢式PCR可对103拷贝/ml的血清样本进行有效特异扩增,新建的RLP检测方法可对PCR扩增产物在1 ng/ml以上,或血清样本中突变型DNA占野生型DNA比例为5%以上的均可有效检测,86例临床的检测灵敏度为100%,野生型和耐药型的检测准确性分别为98.09%(103/105)、100% (43/43),与直接测序法比,RLP检测野生与耐药混合型准确性更好.结论:反向线性探针杂交检测方法检测HBV拉米夫定耐药位点方便、灵敏、准确,是HBV拉米夫定治疗有效的监控工具,该方法适合临床应用.

关 键 词:反向线性探针杂交  乙型肝炎病毒  拉米夫定

Reverse Line Probe Hybridization Assay for Detection of Lamivudine-Resistant Chronic Hepatitis B Virus
LAI Guo-qi , ZHANG Wen-lu , HU Yuan , TANG Hong , ZHANG Lei , XIE Su-lan , PAN Yue , WEI Li-wen , HUANG Ai-long.Reverse Line Probe Hybridization Assay for Detection of Lamivudine-Resistant Chronic Hepatitis B Virus[J].Journal of Southwest China Normal University(Natural Science),2012,37(3):113-119.
Authors:LAI Guo-qi  ZHANG Wen-lu  HU Yuan  TANG Hong  ZHANG Lei  XIE Su-lan  PAN Yue  WEI Li-wen  HUANG Ai-long
Institution:1.Key Laboratory of Molecular Biology on Infectious Diseases,Ministry of Education,Chongqing Medical University,Chongqing 400016,China;2.Laboratory Animal Center,Chongqing Medical University,Chongqing 400016,China
Abstract:Objective: To establish a simple,rapid,sensitive and accurate reserve line probe(RLP) method for the detection of chronic HBV(hepatitis B virus) lamivudine-resistant locus.Methods: Based on the gene sequence of HBV wild-type and lamivudine-resistant drug,universal probe,specific probe of 3’,5’ added poly-C and primers of 5’ labeled biotin were designed.The specific probes were fixed on the nitrocellulose membrane linear;so as to make HBV PCR amplification products hybridize with the probes.By optimizing the hybridization conditions,a reverse line probe hybridization test method was established,which was then used to detect 86 chronic hepatitis B patients in Chongqing,and the results were compared with those of the direct sequencing method.Results: On the condition that HBV DNA in the serum had more than 103 copies/ml,it could be amplified effectively by semi-nested PCR.At the same time,when cDNA was more than 1ng/ml or the mutant proportion was more than 5% in wild-type of serum samples,lamivudine-resistant to chronic hepatitis B virus could be effectively detected by the new RLP hybridization method.The sensitivity in 86 clinic cases was 100%(86/86).The detection accuracy of the wild type and the drug resistant type was 98.09%(103/105),100%(43/43),respectively.Conclusions: The reverse linear probe hybridization method to HBV lamivudine resistance is convenient,sensitive and accurate.It is an effective monitoring tool for HBV lamivudine therapy and suitable for clinical application.
Keywords:reverse line probe hybridization  hepatitis B virus  lamivudine
本文献已被 CNKI 万方数据 等数据库收录!
点击此处可从《西南师范大学学报(自然科学版)》浏览原始摘要信息
点击此处可从《西南师范大学学报(自然科学版)》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号