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通过聚合酶链反应(PCR)结合侧向流动分析快速诊断两种海洋病毒,即牙鲆虹彩病毒和病毒性出血性败血症病毒。

Rapid diagnosis of two marine viruses, red sea bream iridovirus and viral hemorrhagic septicemia virus by PCR combined with lateral flow assay.

作者信息

Seo Haneul, Kil Eui-Joon, Fadhila Chairina, Vo Thuy Thi Bich, Auh Chung-Kyoon, Lee Taek-Kyun, Lee Sukchan

机构信息

College of Biotechnology and Bioengineering, Sungkyunkwan University, 2066 Seobu-ro, Jangan-gu, Suwon, 16419 Korea.

Present Address: Department of Plant Medicals, Andong National University, Andong, 36729 Korea.

出版信息

Virusdisease. 2020 Sep;31(3):251-256. doi: 10.1007/s13337-020-00577-z. Epub 2020 Mar 31.

Abstract

Red sea bream iridovirus (RSIV) and Viral hemorrhagic septicemia virus (VHSV are the most important viral marine pathogens in South Korea because RSIV and VHSV infect and cause high mortality rates in major fish species such as and . These viruses can be transmitted both vertically and horizontally, and early diagnosis is imperative. In this research, RSIV and VHSV viral genomes are detected by PCR-lateral flow assay (LFA). PCR-LFA is sensitive, capable of detecting a viral genome at a concentration of 2-200 fg/µL. Development of this detection method is very meaningful because LFA is simple, requiring a minimum of personnel training to perform. Additionally, LFA requires less time than other detection methods and can be an immediate detection tool that is indispensable in preventing rapid viral spread.

摘要

真鲷虹彩病毒(RSIV)和病毒性出血性败血症病毒(VHSV)是韩国最重要的病毒性海洋病原体,因为RSIV和VHSV会感染诸如 和 等主要鱼类品种并导致高死亡率。这些病毒可通过垂直和水平方式传播,因此早期诊断至关重要。在本研究中,通过聚合酶链反应-侧向流动分析(PCR-LFA)检测RSIV和VHSV病毒基因组。PCR-LFA灵敏度高,能够检测浓度为2-200 fg/µL的病毒基因组。这种检测方法的开发非常有意义,因为侧向流动分析很简单,执行时只需最少的人员培训。此外,侧向流动分析比其他检测方法所需时间更少,并且可以成为预防病毒快速传播不可或缺的即时检测工具。

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