1984
DOI: 10.1007/bf02618871
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Fish cell lines: Establishment and characterization of nine cell lines from salmonids

Abstract: Nine permanent cell lines have been established from five species of salmonids native to America's Pacific Northwest. With the exception of a hepatoma from an adult trout, the lines were derived from normal tissues of embryonic or juvenile fish. Cells were routinely grown in Eagle's minimum essential medium with 10% fetal bovine serum. Optimum growth temperatures for these lines ranged from 21 to 24 degrees C. All survived storage for at least 1 yr at -65 degrees C and at least 5 yr in liquid nitrogen. Six of … Show more

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Cited by 376 publications
(236 citation statements)
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“…Interestingly, the incubation temperature for maximal growth was slightly higher than the preferred temperature (21-28 ° C) of green turtles in nature (15). Wolf (26) suggested culturing fish cells at temperatures slightly above that preferred by the intact animal, and cell lines established from other cold-blooded marine animals similarly show a differential temperature optimum for the host (17,21,22,26). It is currently unclear whether the optimal growth temperature of turtle cells is also optimal for the replication and expression of latent viruses.…”
Section: Discussionmentioning
confidence: 99%
“…Interestingly, the incubation temperature for maximal growth was slightly higher than the preferred temperature (21-28 ° C) of green turtles in nature (15). Wolf (26) suggested culturing fish cells at temperatures slightly above that preferred by the intact animal, and cell lines established from other cold-blooded marine animals similarly show a differential temperature optimum for the host (17,21,22,26). It is currently unclear whether the optimal growth temperature of turtle cells is also optimal for the replication and expression of latent viruses.…”
Section: Discussionmentioning
confidence: 99%
“…As IPNV is ubiquitous in Norwegian salmon farming (Melby et al 1991, Jarp et al 1995, the homogenates were treated with a mix of polyclonal neutralising antibodies against IPNV serotype Sp and serotype Ab. The homogenates were then inoculated onto cell cultures from bluegill fry fibroblast (BF)-2 cells (Wolf & Quimby 1966), epithelioma papulosum cyprini (EPC) (Fijan et al 1983), rainbow trout gonad (RTG)-2 (Wolf & Quimby 1962), chinook salmon embryo (CHSE)-214 (Lannan et al 1984) and Atlantic salmon head kidney (ASK) (Devold et al 2000). Inoculated cells were incubated for 1 wk at both 15 and 20°C in parallel and were regularly investigated with an inverted microscope for the occurrence of a cytopathic effect (CPE).…”
Section: Methodsmentioning
confidence: 99%
“…All IHNV isolates were obtained as virus in frozen cell-culture supernatants prepared using standardized fish health protocols (LaPatra, 1994). Although the exact passage history of some historical isolates could not be obtained, the great majority of the isolates would have been passed only once or twice in fish cellculture lines, such as epithelioma papulosum cyprini cells (Fijan et al, 1983) or chinook salmon embryo 214 cells (Lannan et al, 1984).Sequence analysis. The phylogenetic analysis shown is based on the sequence of a 303 nucleotide region in the middle of the IHNV G gene, referred to as the mid-G sequence (nt 686-988 of the fulllength IHNV G gene sequence; GenBank accession no.…”
mentioning
confidence: 99%