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建立一种用于快速检测家养猫乙型肝炎病毒的直接双路实时 PCR 检测方法。

Development of a direct duplex real-time PCR assay for rapid detection of domestic cat hepadnavirus.

机构信息

Department of Veterinary Science, University of Miyazaki, Miyazaki, Japan.

Faculty of Agriculture; Graduate School of Medicine and Veterinary Medicine, University of Miyazaki, Miyazaki, Japan.

出版信息

J Vet Diagn Invest. 2023 Mar;35(2):139-144. doi: 10.1177/10406387231154610. Epub 2023 Feb 14.

Abstract

Domestic cat hepadnavirus (DCH) is a novel hepadnavirus, first identified in 2018. DCH is generally detected using conventional PCR assays, which include time-consuming agarose gel electrophoresis. We developed a rapid, sensitive, and specific real-time PCR (rtPCR) assay for the detection of the DCH genome. To streamline the procedure, our rtPCR assay was carried out using blood samples, without DNA extraction. A consensus primers/probe set was designed based on the nucleotide sequences of the surface/polymerase gene of all DCH strains available in GenBank. To exclude the possibility that the PCR reaction was blocked by anticoagulants, we also used a primers/probe set for amplifying the cat beta-actin gene as a reference gene. Our direct duplex rtPCR assay had high sensitivity, with a limit of detection of 10 copies/μL of blood for DCH. Our direct duplex rtPCR assay should be a useful tool for DCH detection and surveillance.

摘要

家猫乙型肝炎病毒(DCH)是一种新型乙型肝炎病毒,于 2018 年首次发现。DCH 通常使用包括耗时的琼脂糖凝胶电泳的常规 PCR 检测方法进行检测。我们开发了一种用于检测 DCH 基因组的快速、敏感和特异的实时 PCR(rtPCR)检测方法。为了简化程序,我们的 rtPCR 检测方法使用了未经 DNA 提取的血液样本。根据 GenBank 中所有 DCH 株的表面/聚合酶基因的核苷酸序列,设计了一套共识引物/探针。为了排除抗凝剂阻断 PCR 反应的可能性,我们还使用了用于扩增猫β-肌动蛋白基因的引物/探针作为参考基因。我们的直接双重 rtPCR 检测方法具有很高的灵敏度,DCH 的检测限为 10 拷贝/μL 的血液。我们的直接双重 rtPCR 检测方法应该是 DCH 检测和监测的有用工具。

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