To establish a rapid, sensitive and specific multiplex PCR method for the simultaneous detection ofStaphylococcus aureus,Salmonellaspp, andlisteria monocytogenes. Three pairs of primers have been designed according to theStaphylococcus aureusnucgene,Salmonellaspp IpaBgene,listeria monocytogenes inlAgene. Orthogonal experimental design was used to determine Multiplex PCR amplification system for Food-borne Bacterial Pathogens of four factors (Taq DNA polymerase, Mg2+, dNTP and primers) from four levels; three DNA fragments of 210bp,280bp and 476bp were amplified. The specificity and the sensitivity of this method was valued. Template was prepared using FTA filter; the three food-borne Bacterial Pathogens were simultaneously detected by the multiplex PCR technology which have been designed; The sensitivity of this method was 3.0×102cfu/mL forStaphylococcus aureus, 2.0×102cfu/mL forSalmonellaspp, and 3.5×102cfu/mL forlisteria monocytogenes. This method lies on its accuracy, rapidity and efficiency in the diagnosis, so it could be a useful method for the simultaneous detection of the three species of bacteria in food.
Simultaneous Detection of Four Food Borne Bacterial Pathogens by Metal Hydroxide Immobilised Multiplex PCR Method
