期刊文献+

猪圆环病毒2型环介导等温扩增(LAMP)检测方法的研究 被引量:15

Research of loop-mediated isothermal amplification assay for the detection of porcine circovirus type 2
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摘要 本研究介绍了一种便捷、灵敏而又特异的环介导逆转录等温扩增(LAMP)基因检测技术,该技术分别使用特异对应于靶序列中2对特殊引物,并在Bst DNA聚合酶的作用下对靶序列进行等温核酸扩增反应。本研究对LAMP反应体系和反应条件的优化,结果表明PCV-2 LAMP在63℃1 h内能够成功的检测猪圆环病毒2型基因;敏感性和特异性试验表明,本研究能够特异的检测PCV-2并且其敏感度可以达到10个拷贝的DNA分子,初步研究LAMP的阳性检出率与PCR的阳性检出率比较结果为94%符合。以上结果证明,LAMP扩增技术是一种检测程序简便、灵敏度和特异性较高的基因检测手段,在猪圆环病毒2型的快速检测方面具有一定的开发潜力。 A simple,sensitive LAMP(loop-mediated isothermal amplification) method for the detection of porcine circovirus type 2(PCV2)DNA is described.The method employs a set of four specially designed primers that recognize distinct sequences of the target for sensitive,specific amplification of nucleicacid under isothermal conditions.In this study,through optimization of reaction condition and reaction system,PCV2 LAMP could successfully detect PCV2 in 63℃ per hour;The test of sensitivity and sensitivity indicated that this method was able to detect PCV2 specially and achieved a sensitivity of 10 copy DNA molecules. Initial investigation showed that the positive detection rate of LAMP was 100% comparing the positive detection rate of PCR. Thus, we could conclude that this established LAMP assay has a potential application tO the rapid detection of PCV2.
出处 《中国兽医杂志》 CAS 北大核心 2009年第12期7-10,共4页 Chinese Journal of Veterinary Medicine
基金 国家生猪现代农业产业技术体系基金(hycytx009) 广东省自然科学基金(5006678) 农业部制标项目
关键词 猪圆环病毒2型(PCV-2) 环介导等温扩增(LAMP) 敏感性 特异性 快速检测 porcine circovirus type 2(PCV2) loop-mediated isothermal amplification(LAMP) sensitivity specificity rapid detection
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参考文献15

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二级参考文献46

  • 1申建维,王旭,范春明,孙秀琴,杜万英,万玉梅,彭铁汉,袁玮.多重分子信标环介导等温扩增快速检测耐甲氧西林金黄色葡萄球菌[J].中华医院感染学杂志,2006,16(7):729-733. 被引量:20
  • 2李启明,马学军,周蕊,彭夫望,高寒春,匡治州,侯云德.环介导逆转录等温扩增技术(RT-LAMP)在丙型肝炎病毒基因检测中的应用[J].病毒学报,2006,22(5):334-338. 被引量:55
  • 3Okamoto S, Yoshikawa T, Ihira M, et al. Rapid detection of varicella-zoster virus infection by a loop-mediated isothermal amplification method. J Med Viral, 2004, 74:677-682.
  • 4Horisaka T, Fujita K, Iwata T, et al. Sensitive and specific detection of Yersinia pseudotuberculosis by loop-mediated isothermal amplification. J Clin Microbiol, 2004, 42:5349-5352.
  • 5Yoshikawa T, Ihira M, Akimoto S, et al. Detection of human herpesvirus 7DNA by loop-mediated isothermal amplification. J Clin Microbiol, 2004, 42 : 1348-1352.
  • 6Kuboki N, Inoue N, Sakurai T, et al. Loop-mediated isothermal amplification for detection of african trypanosomes. J Clin Microbiol,2003, 41 : 5517 - 5524.
  • 7Irayama H, Kageyama S, Moriyasu S , et al. Rapid sexing of bovine preimplantation embryos using loop-mediated isothermal amplification.Theriogenology, 2004, 62:887-896.
  • 8Mori Y, Nagamine K, Tomita N, et al. Detection of loop-mediated isothermal amplification reaction by turbidity derived from magnesium pyrophosphate formation. Biochem Biophys Res Commun, 2001,289 : 150-154.
  • 9Nagamine K, Hase T, Notomi T, et al. Accelerated reaction by loop-mediated isothermal amplification using loop primers. Mol Cell Probes , 2002, 16:223-229.
  • 10Nagamine K, Kuzuhara Y, Notomi T, et al. Isolation of single-stranded DNA from loop-mediated isothermal amplification (LAMP)products. Biochem Biophys Res Commun, 2002, 290 : 1195-1198.

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