Soto Esteban, Tamez-Trevino Eva, Yazdi Zeinab, Stevens Brittany N, Yun Susan, Martínez-López Beatriz, Burges Julie
Department of Medicine & Epidemiology, School of Veterinary Medicine, University of California, Davis, California 95616, USA.
Dis Aquat Organ. 2020 Mar 26;138:195-205. doi: 10.3354/dao03456.
Cyprinid herpesvirus 3, also known as koi herpesvirus (KHV), is a viral pathogen responsible for mass mortalities of carp worldwide. In this study, we compared the sensitivity and specificity of ELISA and quantitative PCR (qPCR) methods for the diagnosis of KHV in experimentally infected koi Cyprinus carpio over an 11 mo period. Koi were exposed to KHV at 18 ± 1°C (permissive temperatures for KHV disease) in laboratory-controlled conditions. At 21 d post challenge, the temperature in the system was decreased to <15°C (non-permissive temperature for KHV disease), and fish were monitored for the following 11 mo. At different time points throughout the study, samples of blood and gills were collected from exposed and control koi and subjected to qPCR and ELISA. Survival proportions of 53.3 and 98.8% in exposed and control treatments, respectively, were recorded at the end of the challenge. Traditional receiver-operating characteristic analysis was used to compare the sensitivity of the ELISA and blood and gill qPCR during permissive and non-permissive temperatures. ELISA was superior to qPCR of gills and whole-blood samples in detecting previous exposure to KHV. Similar results were obtained in a second experiment exposing koi to KHV and inducing persistent infection at >30°C (non-permissive temperature for KHV disease). Finally, KHV ELISA specificity was confirmed using cyprinid herpesvirus 1-exposed koi through a period of 3 mo. This study demonstrates that the combination of ELISA and gill qPCR should be recommended in the diagnosis of KHV exposure of suspected carrier-state fish.
鲤疱疹病毒3,也称为锦鲤疱疹病毒(KHV),是一种导致全球鲤鱼大量死亡的病毒病原体。在本研究中,我们比较了酶联免疫吸附测定(ELISA)和定量聚合酶链反应(qPCR)方法在11个月期间对实验感染锦鲤(Cyprinus carpio)中KHV诊断的敏感性和特异性。锦鲤在实验室控制条件下于18±1°C(KHV疾病的允许温度)暴露于KHV。攻毒后21天,系统温度降至<15°C(KHV疾病的非允许温度),并在接下来的11个月内对鱼进行监测。在整个研究的不同时间点,从暴露和对照锦鲤中采集血液和鳃样本,并进行qPCR和ELISA检测。攻毒结束时,暴露组和对照组的存活比例分别记录为53.3%和98.8%。使用传统的受试者工作特征分析来比较ELISA以及血液和鳃qPCR在允许和非允许温度下的敏感性。在检测先前暴露于KHV方面,ELISA优于鳃和全血样本的qPCR。在第二个实验中,将锦鲤暴露于KHV并在>30°C(KHV疾病的非允许温度)诱导持续感染,也获得了类似结果。最后,通过3个月的时间,使用暴露于鲤疱疹病毒1的锦鲤证实了KHV ELISA的特异性。本研究表明,在诊断疑似携带状态鱼的KHV暴露时,应推荐ELISA和鳃qPCR相结合的方法。