Journal
FISHERIES SCIENCE
Volume 77, Issue 4, Pages 607-613Publisher
SPRINGER JAPAN KK
DOI: 10.1007/s12562-011-0362-7
Keywords
Cryptocaryon irritans; Quantitative PCR (qPCR); Natural aquaculture environment
Categories
Funding
- MEXT
- Japan Science Society [22-738]
- JSPS [21380127]
- Grants-in-Aid for Scientific Research [21380127] Funding Source: KAKEN
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We developed a quantitative PCR assay for detecting the parasitic ciliate Cryptocaryon irritans, which causes white spot disease in marine fishes, from the natural environment. A specific primer set for C. irritans was designed and its high specificity was confirmed in silico: almost all of the sequences deposited in the GenBank nucleotide database were covered, 22/23 for the forward primer and 7/7 for the reverse primer. We estimated that there were 3,415.9 rRNA gene copies per genome of C. irritans. In artificial mixture experiments to validate whether the qPCR assay is applicable to natural samples, the estimated copy numbers showed significantly positive correlations with the number of theronts added (p < 0.001). When we applied this qPCR assay to natural samples collected bimonthly from surface and bottom seawaters at an aquaculture site (water depth, 10 m) from May 2009 to March 2010, we only detected C. irritans (112.0 +/- A 6.3 cells/l) in the surface seawater sample in November. This qPCR assay is a useful tool for detecting C. irritans rapidly and quantitatively in natural environments; it could also help advance our understanding of the ecology of C. irritans, as well as facilitate the diagnosis of the disease.
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