A multiplex PCR for the simultaneous detection of Tenacibaculum maritimum and Edwardsiella tarda in aquaculture

Autors/ores

  • Nuria Castro Departamento de Microbiología y Parasitología Facultad de Biología/CIBUS. Universidad de Santiago de Compostela. Santiago de Compostela.
  • Alicia E. Toranzo Department of Microbiology and Parasitology, Faculty of Biology/CIBUS, University of Santiago de Compostela, Santiago de Compostela.
  • Beatriz Magariños Department of Microbiology and Parasitology, Faculty of Biology/CIBUS, University of Santiago de Compostela, Santiago de Compostela.

Paraules clau:

Tenacibaculum maritimum, Edwardsiella tarda, multiplex PCR, fish pathology, aquaculture

Resum

A specific and sensitive multiplex PCR (mPCR) method was developed as a useful tool for the simultaneous detection of two important flatfish pathogens in marine aquaculture, Tenacibaculum maritimum and Edwardsiella tarda. In fish tissues, the average detection limit for these mPCR-amplified organisms was 2 × 105 ± 0.2 CFU/g and 4 × 105 ± 0.3 CFU/g, respectively. These values are similar or even lower than those previously obtained using the corresponding single PCR. Moreover, mPCR did not produce any nonspecific amplification products when tested against 36 taxonomically related and unrelated strains belonging to 33 different bacterial species. Large amounts of DNA from one of the target bacterial species in the presence of low amounts from the other did not have a significant effect on the amplification sensitivity of the latter. [Int Microbiol 2014; 17(2):111-117]

Keywords: Tenacibaculum maritimum · Edwardsiella tarda · multiplex PCR · fish pathology · aquaculture

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