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Development and Application of Quantitative Detection Method for Viral Hemorrhagic Septicemia Virus (VHSV) Genogroup IVa

机译:病毒性出血性败血病病毒基因组IVa定量检测方法的开发与应用

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摘要

Viral hemorrhagic septicemia virus (VHSV) is a problematic pathogen in olive flounder (Paralichthys olivaceus) aquaculture farms in Korea. Thus, it is necessary to develop a rapid and accurate diagnostic method to detect this virus. We developed a quantitative RT-PCR (qRT-PCR) method based on the nucleocapsid (N) gene sequence of Korean VHSV isolate (Genogroup IVa). The slope and R2 values of the primer set developed in this study were −0.2928 (96% efficiency) and 0.9979, respectively. Its comparison with viral infectivity calculated by traditional quantifying method (TCID50) showed a similar pattern of kinetic changes in vitro and in vivo. The qRT-PCR method reduced detection time compared to that of TCID50, making it a very useful tool for VHSV diagnosis.
机译:病毒性出血性败血病病毒(VHSV)是韩国橄榄比目鱼(Paralichthys olivaceus)水产养殖场中有问题的病原体。因此,有必要开发一种快速准确的诊断方法来检测这种病毒。我们基于韩国VHSV分离株(Genogroup IVa)的核衣壳(N)基因序列开发了定量RT-PCR(qRT-PCR)方法。本研究开发的引物组的斜率和R 2 值分别为-0.2928(效率96%)和0.9979。它与通过传统定量方法(TCID50)计算的病毒感染性的比较显示出体内和体外动力学变化的相似模式。与TCID50相比,qRT-PCR方法减少了检测时间,使其成为VHSV诊断的非常有用的工具。

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