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用于鉴定牛星状病毒脑炎的准确和精确的实时 RT-PCR 检测方法。

Accurate and precise real-time RT-PCR assays for the identification of astrovirus associated encephalitis in cattle.

机构信息

NeuroCenter, Division of Neurological Sciences, Vetsuisse Faculty, University of Bern, Bern, Switzerland.

Graduate School for Cellular and Biomedical Sciences, University of Bern, Bern, Switzerland.

出版信息

Sci Rep. 2018 Jun 15;8(1):9215. doi: 10.1038/s41598-018-27533-8.

DOI:10.1038/s41598-018-27533-8
PMID:29907784
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6003944/
Abstract

A novel bovine astrovirus genotype species (BoAstV-CH13/NeuroS1) was recently identified in brain tissues of cattle as a plausible cause of encephalitis. The purpose of the present study was to develop and validate real time RT-PCR assays for the detection of BoAstV-CH13/NeuroS1 in brain tissues of cattle. Three different primer-probe combinations were designed based on BoAstV-CH13/NeuroS1 full-genome sequences of 11 different strains identified in cattle, and established in three distinct one-step real time RT-PCR protocols. These protocols were compared regarding their diagnostic performance using brain tissues of cattle with and without astrovirus associated encephalitis. The limit of detection (LOD) of all three assays was between 1.34 × 10 and 1.34 × 10 RNA copies, leading to an analytical sensitivity two orders of magnitude superior compared to a conventional pan-astrovirus RT-PCR protocol (LOD 1.31 × 10 RNA copies). Amplification efficiency was in the range of 97.3% to 107.5% with linearity (R) > 0.99. The diagnostic sensitivity and specificity of the assays was determined as 100%, and all three revealed good intra- and inter-test repeatability. In conclusion, the newly developed RT-qPCRs are sensitive, specific, and reliable test formats that will facilitate BoAstV-CH13/NeuroS1 detection in routine diagnostics as well as in research settings.

摘要

一种新型牛星状病毒基因型(BoAstV-CH13/NeuroS1)最近在牛脑组织中被鉴定为脑炎的可能病因。本研究旨在开发和验证实时 RT-PCR 检测方法,用于检测牛脑组织中的 BoAstV-CH13/NeuroS1。基于从牛中鉴定出的 11 种不同株的 BoAstV-CH13/NeuroS1 全基因组序列,设计了三种不同的引物-探针组合,并建立了三种不同的一步式实时 RT-PCR 方案。使用有和无星状病毒相关性脑炎的牛脑组织比较了这三种方案的诊断性能。所有三种检测方法的检测限(LOD)均在 1.34×10和 1.34×10 RNA 拷贝之间,与传统的 pan-astrovirus RT-PCR 方案(LOD 为 1.31×10 RNA 拷贝)相比,分析灵敏度提高了两个数量级。扩增效率在 97.3%至 107.5%之间,线性度(R)>0.99。检测方法的诊断灵敏度和特异性均为 100%,所有三种方法均显示出良好的内和间测试重复性。总之,新开发的 RT-qPCR 是敏感、特异和可靠的检测方法,将有助于 BoAstV-CH13/NeuroS1 在常规诊断和研究环境中的检测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/432d/6003944/e58df72c20ff/41598_2018_27533_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/432d/6003944/512d1700677f/41598_2018_27533_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/432d/6003944/df6fd509a2fe/41598_2018_27533_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/432d/6003944/e58df72c20ff/41598_2018_27533_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/432d/6003944/512d1700677f/41598_2018_27533_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/432d/6003944/df6fd509a2fe/41598_2018_27533_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/432d/6003944/e58df72c20ff/41598_2018_27533_Fig3_HTML.jpg

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