Objective To establish a rapid method for detecting Campylobacter jejuni viable bacteria by ethidium monoazide bromide-loop-mediated isothermal amplification (EMA-LAMP). Methods The mapA gene was used as the target gene for LAMP assay of Campylobacter jejuni, and LAMP assay was carried out by utilizing its isolation culture as the template. The sensitivity test for LAMP, the light exposure time and EMA concentration were optimized. Results LAMP detection sensitivity of Campylobacter jejuni was 800 CFU/mL. The exposure time was 5 min. When the final concentration of EMA was below 50 μg/mL, the DNA amplification of viable Campylobacter jejuni was not inhibited. When the final concentration of EMA was 1 μg/mL, and the amplification of dead Campylobacter jejuni was effectively inhibited at 4×104 CFU/mL. The results of EMA-LAMP in 1% of the live bacteria mixture were positive. Conclusion The method of EMA-LAMP can detect Campylobacter jejuni efficiently and rapidly.
标题:叠氮溴乙锭-环介导等温扩增法快速检测空肠弯曲菌活菌
英文标题:Rapid detection of viable Campylobacter jejuni by ethidium monoazide bromide loop-mediated isothermal amplification