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用 2 节段特异性定量 RT-PCR 检测托金伯格环形病毒。

Detection of Toggenburg Orbivirus by a segment 2-specific quantitative RT-PCR.

机构信息

Institute of Virology and Immunoprophylaxis, CH-3147 Mittelhaeusern, Switzerland.

出版信息

J Virol Methods. 2010 May;165(2):325-9. doi: 10.1016/j.jviromet.2010.02.027. Epub 2010 Feb 26.

Abstract

Toggenburg Orbivirus (TOV) has been detected recently in healthy goats in Switzerland. The virus is related closely to bluetongue virus (BTV) and is considered tentatively as a 25th serotype of BTV. Upon detection of additional TOV-positive goats in Switzerland, Germany, and Italy, these TOV isolates were characterized genetically by partial sequencing of the viral genome segment 2 which encodes VP2, the major outer capsid protein of orbiviruses. A TOV-specific RT-qPCR was developed, targeting conserved areas within segment 2. Since TOV cannot be propagated up to now outside its natural host, a synthetic positive control for the RT-qPCR was constructed by cloning the entire coding region of segment 2 and subsequent in vitro transcription of RNA from both ends to obtain double-stranded RNA. The TOV-specific RT-qPCR was able to detect as few as 30 dsRNA copies and proved to be equally sensitive as a pan BTV assay that was shown previously to have a detection limit of 0.001 TCID(50).

摘要

托高甘病毒(Toggenburg Orbivirus,TOV)最近在瑞士健康的山羊中被检测到。该病毒与蓝舌病毒(Bluetongue virus,BTV)密切相关,被暂定为 BTV 的第 25 种血清型。在瑞士、德国和意大利检测到更多的 TOV 阳性山羊后,对这些 TOV 分离株进行了遗传特征分析,方法是对编码 orbiviruses 主要外壳蛋白 VP2 的病毒基因组片段 2 进行部分测序。开发了一种针对 2 号片段内保守区域的 TOV 特异性 RT-qPCR。由于到目前为止,TOV 还不能在其自然宿主之外进行繁殖,因此通过克隆 2 号片段的整个编码区并从两端进行体外转录 RNA 来构建用于 RT-qPCR 的合成阳性对照,以获得双链 RNA。TOV 特异性 RT-qPCR 能够检测到低至 30 个 dsRNA 拷贝,并且与先前显示检测限为 0.001 TCID(50)的 pan BTV 检测方法一样敏感。

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