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三种检测鲤疱疹病毒3型(CyHV-3)方法的诊断验证

Diagnostic validation of three test methods for detection of cyprinid herpesvirus 3 (CyHV-3).

作者信息

Clouthier Sharon C, McClure Carol, Schroeder Tamara, Desai Megan, Hawley Laura, Khatkar Sunita, Lindsay Melissa, Lowe Geoff, Richard Jon, Anderson Eric D

机构信息

Fisheries and Oceans Canada, Freshwater Institute, 501 University Crescent, Winnipeg, Manitoba R3T 2N6, Canada.

出版信息

Dis Aquat Organ. 2017 Mar 6;123(2):101-122. doi: 10.3354/dao03093.

Abstract

Cyprinid herpesvirus 3 (CyHV-3) is the aetiological agent of koi herpesvirus disease in koi and common carp. The disease is notifiable to the World Organisation for Animal Health. Three tests-quantitative polymerase chain reaction (qPCR), conventional PCR (cPCR) and virus isolation by cell culture (VI)-were validated to assess their fitness as diagnostic tools for detection of CyHV-3. Test performance metrics of diagnostic accuracy were sensitivity (DSe) and specificity (DSp). Repeatability and reproducibility were measured to assess diagnostic precision. Estimates of test accuracy, in the absence of a gold standard reference test, were generated using latent class models. Test samples originated from wild common carp naturally exposed to CyHV-3 or domesticated koi either virus free or experimentally infected with the virus. Three laboratories in Canada participated in the precision study. Moderate to high repeatability (81 to 99%) and reproducibility (72 to 97%) were observed for the qPCR and cPCR tests. The lack of agreement observed between some of the PCR test pair results was attributed to cross-contamination of samples with CyHV-3 nucleic acid. Accuracy estimates for the PCR tests were 99% for DSe and 93% for DSp. Poor precision was observed for the VI test (4 to 95%). Accuracy estimates for VI/qPCR were 90% for DSe and 88% for DSp. Collectively, the results show that the CyHV-3 qPCR test is a suitable tool for surveillance, presumptive diagnosis and certification of individuals or populations as CyHV-3 free.

摘要

鲤疱疹病毒3型(CyHV-3)是锦鲤和鲤鱼患锦鲤疱疹病毒病的病原体。该病需向世界动物卫生组织通报。三种检测方法——定量聚合酶链反应(qPCR)、常规PCR(cPCR)和细胞培养病毒分离法(VI)——经过验证,以评估其作为检测CyHV-3诊断工具的适用性。诊断准确性的检测性能指标为灵敏度(DSe)和特异性(DSp)。通过测量重复性和再现性来评估诊断精度。在没有金标准参考检测的情况下,使用潜在类别模型生成检测准确性估计值。检测样本来自自然感染CyHV-3的野生鲤鱼或未感染病毒或经实验感染该病毒的养殖锦鲤。加拿大的三个实验室参与了精度研究。qPCR和cPCR检测的重复性(81%至99%)和再现性(72%至97%)为中度到高度。部分PCR检测对结果之间缺乏一致性,这归因于样本被CyHV-3核酸交叉污染。PCR检测的准确性估计值为DSe 99%,DSp 93%。VI检测的精度较差(4%至95%)。VI/qPCR的准确性估计值为DSe 90%,DSp 88%。总体而言,结果表明CyHV-3 qPCR检测是监测、初步诊断以及证明个体或群体未感染CyHV-3的合适工具。

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