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利用环介导等温扩增检测技术检测韩国猪群中的新型猪圆环病毒 4。

Detection of a novel porcine circovirus 4 in Korean pig herds using a loop-mediated isothermal amplification assay.

机构信息

College of Veterinary Medicine & Animal Disease Intervention Center, Kyungpook National University, Daegu, 41566, Republic of Korea.

College of Veterinary Medicine & Animal Disease Intervention Center, Kyungpook National University, Daegu, 41566, Republic of Korea; DIVA Bio Incorporation, Daegu, 41519, Republic of Korea.

出版信息

J Virol Methods. 2022 Jan;299:114350. doi: 10.1016/j.jviromet.2021.114350. Epub 2021 Nov 5.

Abstract

A novel porcine circovirus 4 has been recently identified in China and Korea. A sensitive and specific diagnostic method is urgently required to detect the virus in field samples. We developed a loop-mediated isothermal amplification (LAMP) the assay for the visual detection of PCV4 and evaluated its sensitivity, specificity, and applicability in clinical samples. This assay's results can be directly visualized by the naked eye using hydroxynaphthol blue after incubation for 40 min at 64 °C. The assay specifically amplified PCV4 DNA and no other viral nucleic acids. The sensitivity of the assay was <50 DNA copies/reaction, which was 10 times more sensitive than conventional polymerase chain reaction (cPCR) and comparable to real-time PCR (qPCR). Clinical evaluation revealed that the PCV4 detection rate in individual pig samples and at the farm level was 39.3 % (57/145) and 45.7 % (32/70), respectively, which were higher than cPCR (46 samples, 24 farms) and qPCR (52 samples, 29 farms) results. Cumulatively, owing to the advantages of high sensitivity and specificity, direct visual monitoring of the results, no possibility for cross-contamination, and being a low-cost equipment, the developed LAMP assay will be a valuable tool for the detection of the novel PCV4 in clinical samples, even in resource-limited laboratories.

摘要

一种新型猪圆环病毒 4 最近在中国和韩国被发现。迫切需要一种敏感和特异的诊断方法来检测现场样本中的病毒。我们开发了一种用于检测 PCV4 的环介导等温扩增(LAMP)检测方法,并评估了其在临床样本中的敏感性、特异性和适用性。该检测方法在 64°C 孵育 40 分钟后,可通过肉眼直接观察羟萘酚蓝来判断结果。该检测方法特异性扩增 PCV4 DNA,而不扩增其他病毒核酸。该检测方法的灵敏度低至 50 个 DNA 拷贝/反应,比常规聚合酶链反应(cPCR)灵敏 10 倍,与实时 PCR(qPCR)相当。临床评估显示,个体猪样本和农场水平的 PCV4 检出率分别为 39.3%(57/145)和 45.7%(32/70),高于 cPCR(46 个样本,24 个农场)和 qPCR(52 个样本,29 个农场)的结果。总的来说,由于该检测方法具有高灵敏度和特异性、结果可直接肉眼观察、无交叉污染的可能性以及成本低的设备等优点,因此将成为一种有价值的工具,用于检测临床样本中的新型 PCV4,即使在资源有限的实验室也是如此。

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