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Development and validation of a real-time PCR assay for the detection of Aeromonas salmonicida.

Authors :
Keeling, S E
Brosnahan, C L
Johnston, C
Wallis, R
Gudkovs, N
McDonald, W L
Source :
Journal of Fish Diseases. May2013, Vol. 36 Issue 5, p495-503. 9p. 4 Charts, 3 Graphs.
Publication Year :
2013

Abstract

A real-time PCR assay using a molecular beacon was developed and validated to detect the vapA (surface array protein) gene in the fish pathogen, Aeromonas salmonicida. The assay had 100% analytical specificity and analytical sensitivities of 5 ± 0 fg ( DNA), 2.2 × 104 ± 1 × 104 CFU g−1 (without enrichment) and 40 ± 10 CFU g−1 (with enrichment) in kidney tissue. The assay was highly repeatable and proved to be robust following equivalency testing using a different real-time PCR platform. Following analytical validation, diagnostic specificity was determined using New Zealand farmed Chinook salmon, Oncorhynchus tshawytscha ( Walbaum), ( n = 750) and pink shubunkin, Carassius auratus ( L.) ( n = 157). The real-time PCR was run in parallel with culture and all fish tested were found to be negative by both methods for A. salmonicida, resulting in 100% diagnostic specificity (95% confidence interval). The molecular beacon real-time PCR system is specific, sensitive and a reproducible method for the detection of A. salmonicida. It can be used for diagnostic testing, health certification and active surveillance programmes. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01407775
Volume :
36
Issue :
5
Database :
Academic Search Index
Journal :
Journal of Fish Diseases
Publication Type :
Academic Journal
Accession number :
86882108
Full Text :
https://doi.org/10.1111/jfd.12014