首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Visual Detection of High-Risk Human Papillomavirus Genotypes 16 18 45 52 and 58 by Loop-Mediated Isothermal Amplification with Hydroxynaphthol Blue Dye
【2h】

Visual Detection of High-Risk Human Papillomavirus Genotypes 16 18 45 52 and 58 by Loop-Mediated Isothermal Amplification with Hydroxynaphthol Blue Dye

机译:视觉检测高风险的人乳头瘤病毒基因型16、18、45、52和58通过羟肟酚蓝染料的环介导等温扩增

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

A simple, rapid, sensitive, qualitative, colorimetric loop-mediated isothermal amplification (LAMP) with hydroxynaphthol blue dye (HNB) was established to detect high-risk human papillomavirus (HPV) genotypes 16, 18, 45, 52, and 58. All initial validation studies with the control DNA proved to be type specific. The colorimetric type-specific LAMP assay could achieve a sensitivity of 10 to 100 copies at 63°C for 65 min, comparable to that of real-time PCR. In order to evaluate the reliability of HPV type-specific LAMP, the assay was further evaluated with HPV DNAs from a panel of 294 clinical specimens whose HPV status was previously determined with a novel one-step typing method with multiplex PCR. The tested panel comprised 108 HPV DNA-negative samples and 186 HPV-DNA-positive samples of 14 genotypes. The results showed that the sensitivity of HPV type-specific LAMP for HPV types 16, 18, 45, 52, and 58 was 100%, 100%, 100%, 100%, and 100%, respectively, and the specificity was 100%, 98.5%, 100%, 98.8%, and 99.2%, respectively, compared with a novel one-step typing method with multiplex PCR. No cross-reactivity with other HPV genotypes was observed. In conclusion, this qualitative and colorimetric LAMP assay has potential usefulness for the rapid screening of HPV genotype 16, 18, 45, 52, and 58 infections, especially in resource-limited hospitals or rural clinics of provincial and municipal regions in China.
机译:建立了一种简单,快速,灵敏,定性,比色环介导的羟萘酚蓝染料(HNB)等温扩增(LAMP)方法,以检测高风险的人乳头瘤病毒(HPV)基因型16、18、45、52和58。对照DNA的初步验证研究被证明是类型特异性的。比色类型特异性LAMP分析在63°C的条件下65分钟可以达到10到100个拷贝的灵敏度,这与实时PCR相当。为了评估HPV类型特异性LAMP的可靠性,进一步对来自294个临床标本的HPV DNA进行了分析评估,这些标本先前已通过新颖的单步分型方法通过多重PCR确定了HPV状态。所测试的组包括108个HPV DNA阴性样品和186个HPV DNA阳性样品,分别具有14个基因型。结果表明,HPV型特异性LAMP对16、18、45、52和58型HPV的敏感性分别为100%,100%,100%,100%和100%,特异性为100%与一种新颖的多重PCR分型方法相比,分别为98.5%,100%,98.8%和99.2%。没有观察到与其他HPV基因型的交叉反应。总而言之,这种定性和比色的LAMP测定法可用于快速筛查HPV基因型16、18、45、52和58感染,特别是在中国省市级资源有限的医院或农村诊所中。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号