2018
DOI: 10.1016/j.aquaculture.2018.04.041
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Molecular diagnostics for verifying an etiological agent of emaciation disease in cultured olive flounder Paralichthys olivaceus in Korea

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Cited by 13 publications
(20 citation statements)
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“…However, when analysing the infection levels in all intestinal segments, there was no time effect at high temperature (T1) in terms of prevalence of infection, whereas at low temperature (T2), the effect of time was clear. Time of exposure was also negatively correlated with growth performance, according to the emaciative effect induced by E. leei infections on GSB and olive flounder (Shin, Sohn, Jin, Kang, & Lee, ; Sitjà‐Bobadilla & Palenzuela, ). Consequently, T1R2‐1 fish reached the highest weight, and T2R2‐1 fish, the best condition factor at the end of each trial.…”
Section: Discussionmentioning
confidence: 99%
“…However, when analysing the infection levels in all intestinal segments, there was no time effect at high temperature (T1) in terms of prevalence of infection, whereas at low temperature (T2), the effect of time was clear. Time of exposure was also negatively correlated with growth performance, according to the emaciative effect induced by E. leei infections on GSB and olive flounder (Shin, Sohn, Jin, Kang, & Lee, ; Sitjà‐Bobadilla & Palenzuela, ). Consequently, T1R2‐1 fish reached the highest weight, and T2R2‐1 fish, the best condition factor at the end of each trial.…”
Section: Discussionmentioning
confidence: 99%
“…Recent studies have identified that E. leei is the causative agent of emaciation disease that has caused great economic loss to the cultured olive flounder industry in Korea, especially in Jeju Island (Sekiya et al., ; Shin et al., ). In addition, Yasuda et al.…”
Section: Discussionmentioning
confidence: 99%
“…For quantification of the intensity of E. leei infection, partial 18S rDNA PCR amplicons from an infected olive flounder were cloned and used as standard controls to generate a standard curve. Briefly, PCR amplification was performed using the following primers that had been designed in a previous study (Shin et al., ): ELNMF: CGGTGACGCCAATCCGTG and MyNMR: GACGGTATCTGATCGTCTTCGA. PCR condition were as follows: initial denaturation at 94°C for 5 min, 35 cycles of denaturation at 94°C for 30 s, annealing at 58°C for 30 s, extension at 72°C for 30 s and a final extension step at 72°C for 7 min.…”
Section: Methodsmentioning
confidence: 99%
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