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Development of diagnostic assays for differentiation of atypical Aeromonas salmonicida vapA type V and type VI in ballan wrasse ( Labrus bergylta , Ascanius)

Athina Papadopoulou; Andrew Davie; Sean J. Monaghan; Herve Migaud; Alexandra Adams
Journal of Fish Diseases · Vol. 44, Issue 6 · pp. 711-719 · 2021

Abstract

Aeromonas salmonicida ( As ) is a highly heterogeneous bacterial species, and strains’ host specificity has been reported. Ballan wrasse ( Labrus bergylta Ascanius, 1767) is susceptible to atypical As (a As ) vapA type V and type VI in Scotland and Norway. Identification of the bacterium is achieved by culture and molecular techniques; however, the available methods used to distinguish the As types are costly and time‐consuming. This paper describes the development of a PCR and a restriction enzyme assay for the detection of a As vapA type V and type VI in ballan wrasse, respectively. Type V‐specific primers were designed on conserved regions of the vapA gene, and the restriction enzyme assay was performed on the PCR products of the hypervariable region of vapA gene for the detection of type VI isolates. Amplification product was produced for type V (254 bp) and restriction bands (368 and 254 bp) for type VI isolates only. In addition, the assays detected type V and type VI isolates in spiked water samples and type V in diagnostic tissue samples. The assays are fast, specific and cost‐effective and can be used as specific diagnostic tools for cleaner fish, to detect infectious divergence strains, and to manage and mitigate a As disease outbreaks through vaccine development.

Bibliographic Information

JournalJournal of Fish Diseases
PublisherWiley
Publication Date2021-06-01
Publication Year2021
Volume44
Issue6
Pages711-719
Document TypeJournal Article
Print ISSN0140-7775
eISSN1365-2761
DOI10.1111/jfd.13334
SubjectGeneral Aquaculture, Fisheries & Fish Science

Access Information

NARA Access Coverage1997-01-01~Current
Journal Homepagehttps://onlinelibrary.wiley.com/loi/13652761
Publisher PageOpen Publisher Page
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