O157:H7, , and are food-borne pathogens that cause serious gastrointestinal illness and frequent food safety accidents. This study aimed to develop a practical multiplex polymerase chain reaction (mPCR) technique for the simultaneous detection of these food-borne pathogens in culture broth and artificial food matrix. Pathogen-specific DNA sequences in the E, , and A genes were used as targets to design primers for the identification of O157:H7, , and respectively. As expected, the method produced species-specific bands of amplified products without any contaminating non-specific bands. The highest species specificity was established with primer concentrations of 0.1, 0.2, and 0.4 μM for O157:H7, , and , correspondingly. The detection sensitivity of this assay was 10 CFU/mL in culture broth, and the limit of detection was consistent with singleplex PCR in the food sample. The mPCR assay proposed here is an easy and convenient detection method, which will be valuable for microbial epidemiology and food safety investigations.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5767162 | PMC |
http://dx.doi.org/10.1007/s13205-018-1086-5 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!