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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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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)水产养殖场中一个有问题的病原体。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。本研究开发的引物对的斜率和R 2 值分别为-0.2928(效率96%)和0.9979。与传统定量方法(TCID 50 )计算出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TCID 50 相比,qRT-PCR方法减少了检测时间,使其成为诊断VHSV的非常有用的工具。

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