2006
DOI: 10.1016/j.aquaculture.2005.12.015
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Molecular comparison of iridoviruses isolated from marine fish cultured in Korea and imported from China

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Cited by 28 publications
(27 citation statements)
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“…These findings suggest a potential risk of ISKNV disease in various freshwater ornamental fish species, including the 7 species that were 1-step PCR negative, in which clinical signs and mortality were not observed. Jeong et al (2006b) reported many different types of repetitive sequences in the genome of iridoviruses isolated from marine fish, especially as a cluster form in the 3' terminal region of the ORF-2 gene of the K2 region. Such repetitive sequences might be variable in individual fish or depend on the iridovirus strain as those found in the ORF-1 gene (Jeong et al 2006a).…”
Section: Discussionmentioning
confidence: 99%
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“…These findings suggest a potential risk of ISKNV disease in various freshwater ornamental fish species, including the 7 species that were 1-step PCR negative, in which clinical signs and mortality were not observed. Jeong et al (2006b) reported many different types of repetitive sequences in the genome of iridoviruses isolated from marine fish, especially as a cluster form in the 3' terminal region of the ORF-2 gene of the K2 region. Such repetitive sequences might be variable in individual fish or depend on the iridovirus strain as those found in the ORF-1 gene (Jeong et al 2006a).…”
Section: Discussionmentioning
confidence: 99%
“…Determined nucleotide sequences of the open reading frame (ORF)-2 region (Jeong et al 2006b) of SGIV-1 and PGIV-3 have been submitted to GenBank (accession no. DQ812903 and DQ812904, respectively).…”
Section: Methodsmentioning
confidence: 99%
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“…Cromileptes altivelis sleepy disease virus (GSDIV), and RBIV IVS-1 (He et al 2000, Hanson et al 2001, Sudthongkong et al 2002, Do et al 2004, Mahardika et al 2004, Jeong et al 2006a. Iridoviral replication via cell culture is inefficient; thus, each of these viruses is difficult to cultivate in vitro (Nakajima & Sorimachi 1994, Chou et al 1998.…”
Section: Aplocheilichthys Normani Iridovirus (Aliv) Dwarf Gourami Comentioning
confidence: 99%
“…To determine the phylogenetic relationships between iridoviruses, or for detection of a given iridovirus, previous studies have used polymerase chain reaction (PCR) with primers specific for various genes, including major capsid protein (MCP) (He et al 2001), ribonucleotide reductase small subunit (RNRS) (Oshima et al 1998), DNA polymerase (DPOL), adenosine triphosphatase (ATPase), the Pst I restriction fragment (Kurita et al 1998), and K2 region (Jeong et al 2006a). However, PCR-based assays are only able to detect the presence of an iridoviral infection, and not the viral load in the infected fish, which may be a useful indicator of disease outbreaks.…”
Section: Transmission Of Iridovirus From Freshwater Ornamental Fish (mentioning
confidence: 99%