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多重扩增难治突变系统聚合酶链反应(ARMS-PCR)可对犬细小病毒进行无需测序的分型。

Multiplex Amplification Refractory Mutation System PCR (ARMS-PCR) provides sequencing independent typing of canine parvovirus.

作者信息

Chander Vishal, Chakravarti Soumendu, Gupta Vikas, Nandi Sukdeb, Singh Mithilesh, Badasara Surendra Kumar, Sharma Chhavi, Mittal Mitesh, Dandapat S, Gupta V K

机构信息

ICAR-Indian Veterinary Research Institute, Izatnagar, Bareilly, UP 243122, India.

ICAR-Indian Veterinary Research Institute, Izatnagar, Bareilly, UP 243122, India.

出版信息

Infect Genet Evol. 2016 Dec;46:59-64. doi: 10.1016/j.meegid.2016.10.024. Epub 2016 Oct 29.

Abstract

Canine parvovirus-2 antigenic variants (CPV-2a, CPV-2b and CPV-2c) ubiquitously distributed worldwide in canine population causes severe fatal gastroenteritis. Antigenic typing of CPV-2 remains a prime focus of research groups worldwide in understanding the disease epidemiology and virus evolution. The present study was thus envisioned to provide a simple sequencing independent, rapid, robust, specific, user-friendly technique for detecting and typing of presently circulating CPV-2 antigenic variants. ARMS-PCR strategy was employed using specific primers for CPV-2a, CPV-2b and CPV-2c to differentiate these antigenic types. ARMS-PCR was initially optimized with reference positive controls in two steps; where first reaction was used to differentiate CPV-2a from CPV-2b/CPV-2c. The second reaction was carried out with CPV-2c specific primers to confirm the presence of CPV-2c. Initial validation of the ARMS-PCR was carried out with 24 sequenced samples and the results were matched with the sequencing results. ARMS-PCR technique was further used to screen and type 90 suspected clinical samples. Randomly selected 15 suspected clinical samples that were typed with this technique were sequenced. The results of ARMS-PCR and the sequencing matched exactly with each other. The developed technique has a potential to become a sequencing independent method for simultaneous detection and typing of CPV-2 antigenic variants in veterinary disease diagnostic laboratories globally.

摘要

犬细小病毒2型抗原变异体(CPV-2a、CPV-2b和CPV-2c)在全球犬类群体中广泛分布,可引发严重的致命性胃肠炎。CPV-2的抗原分型仍是全球研究团队在了解疾病流行病学和病毒进化方面的首要关注重点。因此,本研究旨在提供一种简单的、无需测序的、快速、稳健、特异且用户友好的技术,用于检测和分型当前流行的CPV-2抗原变异体。采用针对CPV-2a、CPV-2b和CPV-2c的特异性引物的扩增阻滞突变系统聚合酶链反应(ARMS-PCR)策略来区分这些抗原类型。ARMS-PCR最初分两步用参考阳性对照进行优化;第一步反应用于区分CPV-2a与CPV-2b/CPV-2c。第二步反应使用CPV-2c特异性引物进行,以确认CPV-2c的存在。用24个已测序样本对ARMS-PCR进行初步验证,结果与测序结果相符。进一步使用ARMS-PCR技术对90份疑似临床样本进行筛查和分型。对随机选择的15份用该技术分型的疑似临床样本进行测序。ARMS-PCR结果与测序结果完全匹配。所开发的技术有潜力成为一种无需测序的方法,用于全球兽医疾病诊断实验室同时检测和分型CPV-2抗原变异体。

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