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In vitro propagation of tilapia lake virus in cell lines developed from Oreochromis mossambicus

Ravi Nanthini; Seepoo Abdul Majeed; Sugumar Vimal; Gani Taju; Selvam Sivakumar; Shanmugam Santhosh Kumar; Devika Pillai; Kalasseril Girijan Sneha; Chakalaparambil Gokulan Rakesh; Azeez Sait Sahul Hameed
Journal of Fish Diseases · Vol. 42, Issue 11 · pp. 1543-1552 · 2019

Abstract

Tilapia lake virus (TiLV)‐suspected samples of tilapia were collected from grow‐out ponds located with clinical signs and mortality ranged from 5% to 50%. The reverse transcription–polymerase chain reaction (RT‐PCR) assay revealed the presence of TiLV in the disease outbreak ponds. Cell lines were developed from heart, gill and eye of Mozambique tilapia and characterized. Morphologically, these cell lines are composed of epithelioid cells. The optimum growth of these cells was observed at 28°C and 20% concentration of FBS. After cryopreservation, 70%–90% of cells were found to be viable. The cells of all three cell lines were found to be positive to fibronectin and pancytokeratin. PCR amplification of 16S rRNA and COI of O. mossambicus confirmed the origin of these cell lines from O. mossambicus . Heart and gill cell lines were found to be highly susceptible to TiLV and found to be useful for its isolation from infected fish samples. The experimental infection was carried out in O. niloticus and O. mossambicus using the TiLV propagated in susceptible cell lines. The RT‐PCR results revealed the presence of TiLV in brain, gill, liver, kidney, spleen, eye, muscle, intestine and heart of experimentally infected O. niloticus and O. mossambicus .

Bibliographic Information

JournalJournal of Fish Diseases
PublisherWiley
Publication Date2019-11-01
Publication Year2019
Volume42
Issue11
Pages1543-1552
Document TypeJournal Article
Print ISSN0140-7775
eISSN1365-2761
DOI10.1111/jfd.13075
SubjectGeneral Aquaculture, Fisheries & Fish Science

Access Information

NARA Access Coverage1997-01-01~Current
Journal Homepagehttps://onlinelibrary.wiley.com/loi/13652761
Publisher PageOpen Publisher Page
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