Abstract:
The study establisheda loop-mediated isothermal amplification (LAMP) technology for Aeromonas hydrophila and A.sobria. We designed the primers based on the sequences of the pilin gene of A.hydrophila and the zipA gene of A.sobria, respectively, and conducted specificity and sensitivity tests by real-time turbidimeter under isothermal conditions, which were detected by agarose gel electrophoresis test and change of SYBR Green I colour. The results show that the LAMP method was effective for rapid detection of A.hydrophila and A.sobria with limit of detections of 46 fgmL-1 and 320 fgmL-1, 104 and 102 times more sensitive than the conventional PCR, respectively. In conclusion, the LAMP detective method for A.hydrophila and A.sobria whichwe established was specific, sensitive, effective and rapid.