| Literature DB >> 27974544 |
Japhette Esther Kembou Tsofack1, Rachel Zamostiano1, Salsabeel Watted2, Asaf Berkowitz2, Ezra Rosenbluth2, Nischay Mishra3, Thomas Briese3, W Ian Lipkin3, Richard M Kabuusu4, Hugh Ferguson4, Jorge Del Pozo5, Avi Eldar6, Eran Bacharach7.
Abstract
Tilapia are an important group of farmed fish that serve as a significant protein source worldwide. In recent years, substantial mortality of wild tilapia has been observed in the Sea of Galilee and in commercial ponds in Israel and Ecuador. We have identified the etiological agent of these mass die-offs as a novel orthomyxo-like virus and named it tilapia lake virus (TiLV). Here, we provide the conditions for efficient isolation, culturing, and quantification of the virus, including the use of susceptible fish cell lines. Moreover, we describe a sensitive nested reverse transcription-PCR (RT-PCR) assay allowing the rapid detection of TiLV in fish organs. This assay revealed, for the first time to our knowledge, the presence of TiLV in diseased Colombian tilapia, indicating a wider distribution of this emerging pathogen and stressing the risk that TiLV poses for the global tilapia industry. Overall, the described procedures should provide the tilapia aquaculture industry with important tools for the detection and containment of this pathogen.Entities:
Keywords: PCR; TiLV; diagnosis; tilapia; virus
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Year: 2016 PMID: 27974544 PMCID: PMC5328443 DOI: 10.1128/JCM.01808-16
Source DB: PubMed Journal: J Clin Microbiol ISSN: 0095-1137 Impact factor: 5.948