Suppr超能文献

建立一种通用实时 PCR 检测方法,用于同时检测猴逆转录病毒血清型 1、2、3、4 和 5 的前病毒 DNA,以及用于特定血清型鉴定的二次单重检测方法。

Development of a generic real-time PCR assay for simultaneous detection of proviral DNA of simian Betaretrovirus serotypes 1, 2, 3, 4 and 5 and secondary uniplex assays for specific serotype identification.

机构信息

California National Primate Research Center, University of California, Davis, CA 95616, USA.

出版信息

J Virol Methods. 2009 Dec;162(1-2):148-54. doi: 10.1016/j.jviromet.2009.07.030. Epub 2009 Aug 5.

Abstract

Simian betaretroviruses (formerly Type D retroviruses; SRV) are a group of closely related retroviruses for which the natural host species are Asian monkeys of the genus Macaca. Five serotypes have been identified by classical neutralization assays and three additional untyped variants have been reported (SRV(Tsukuba), SRV-6, SRV-7). These viruses may be significant pathogens in macaque colonies, causing a broad spectrum of clinical disease secondary to viral-induced immune suppression. Undetected SRV infections in research macaques also represent a potential confounding variable in research protocols and a concern for human caretakers. Intensive testing efforts have been implemented to identify infected animals in established colonies. A real-time quantitative generic multiplex PCR assay was developed that is capable of simultaneous detection of proviral DNA of SRV serotypes 1, 2, 3, 4 and 5. This assay incorporates amplification of the oncostatin M (OSM) gene for confirmation of amplifiable DNA and allows quantitation of the number of proviral copies per cell analyzed in each multiplex reaction. Detection of multiple serotypes by PCR increases the efficiency and cost-effectiveness of SRV screening programs. A panel of SRV serotype-specific uniplex real-time PCR assays for discrimination among the five recognized serotypes is also described.

摘要

猿猴逆转录病毒(以前称为 D 型逆转录病毒;SRV)是一组密切相关的逆转录病毒,其自然宿主物种是亚洲猕猴属的猴子。通过经典的中和测定已鉴定出五种血清型,并且还报告了三种额外的未分型变体(SRV(筑波)、SRV-6、SRV-7)。这些病毒可能是猕猴群体中的重要病原体,导致广泛的临床疾病继发于病毒诱导的免疫抑制。在研究用猕猴中未检测到的 SRV 感染也代表了研究方案中的潜在混杂变量,也是人类饲养员关注的问题。已经实施了密集的测试工作来确定已建立的群体中受感染的动物。开发了一种实时定量通用多重 PCR 检测方法,能够同时检测 SRV 血清型 1、2、3、4 和 5 的前病毒 DNA。该检测方法包括对肿瘤坏死因子(OSM)基因的扩增,以确认可扩增的 DNA,并允许定量分析每个多重反应中分析的每个细胞中的前病毒拷贝数。通过 PCR 检测多种血清型可提高 SRV 筛查计划的效率和成本效益。还描述了用于区分五种公认血清型的一组 SRV 血清型特异性单重实时 PCR 检测方法。

相似文献

引用本文的文献

本文引用的文献

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验