Development of a two‐step,non‐probed multiplex real‐time PCR for surveilling Vibrio anguillarum in seawater |
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Authors: | M E Hickey G P Richards J‐L Lee |
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Affiliation: | 1. Department of Human Ecology, Food Science Program, College of Agricultural and Related Sciences, Delaware State University, Dover, DE, USA;2. United States Department of Agriculture, Agricultural Research Service, Dover, DE, USA |
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Abstract: | Vibrio anguillarum is an aggressive and halophilic bacterial pathogen most commonly originating from seawater. Vibrio anguillarum presence in fisheries and aquaculture facilities causes significant morbidity and mortality among aquaculture species primarily from haemorrhaging of the body and skin of the infected fish that eventually leads to death, collectively recognized as the disease vibriosis. This study served to develop a non‐probe, multiplex real‐time PCR assay to rapidly detect V. anguillarum presence in seawater. Specific primers targeting genes vah1, empA and rpoN of V. anguillarum were selected for multiplex reaction among 11 different primer sets and the extension step was eliminated. Primer concentration, denaturation time as well as annealing time and temperature of DNA amplification were optimized, thus reducing reaction duration. The two‐step, non‐probed multiplex real‐time PCR set forth by this study detects as little as 3 CFU mL?1 of V. anguillarum presence in sea water, without enrichment cultivation, in 70 min with molecular precision and includes melting curve confirmation. |
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Keywords: | non‐probed multiplex qPCR seawater thermal factors
Vibrio anguillarum
vibriosis |
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