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Viral susceptibility, transfection and growth of SPB – a fish neural progenitor cell line from the brain of snubnose pompano, T rachinotus blochii ( L acépède)

C‐M Wen; C‐C Ku; C‐S Wang
Journal of Fish Diseases · Vol. 36, Issue 7 · pp. 657-667 · 2013

Abstract

This study investigates the susceptibilities of the SPB cell line to fish viruses including giant seaperch iridovirus ( GSIV ‐ K 1), red sea bream iridovirus ( RSIV ‐ K u), grouper nervous necrosis virus ( GNNV ‐ K 1), chum salmon reovirus ( CSV ) and eel herpesvirus ( HVA ). GSIV ‐ K 1, RSIV ‐ K u and CSV replicated well in SPB cells, with a significant cytopathic effect and virus production. However, the cells were HVA and GNNV refractory. To examine the ability of SPB cells to stably express foreign protein, expression vectors encoding GNNV B 1 and B 2 fused to enhanced green fluorescent protein ( EGFP ) and GSIV ORF 35 L fused to D s R ed were constructed and introduced by transfection into SPB cells. Stable transfectants displayed different morphologies compared with SPB and with each other. EGFP ‐ B 1 was predominantly localized in the nuclei, EFPF ‐ B 2 was distributed throughout the cytoplasm and nucleus, and granular 35 L ‐ D s R ed was localized with secreted vesicles. The expression of EFPF ‐ B 2 in SPB cells produced blebs on the surface, but the cells showing stable expression of EGFP , EGFP ‐ B 1 or 35 L ‐ D s R ed showed normal morphologies. Results show the SPB cells and the transfected cells grow well at temperatures between 20 and 35 °C and with serum‐dependent growth. SPB cells are suitable for studies on foreign protein expression and virology.

Bibliographic Information

JournalJournal of Fish Diseases
PublisherWiley
Publication Date2013-07-01
Publication Year2013
Volume36
Issue7
Pages657-667
Document TypeJournal Article
Print ISSN0140-7775
eISSN1365-2761
DOI10.1111/jfd.12067
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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