Improved Method for Detecting Salmonella During Poultry Processing14 May 2015
A recently completed research project at the University of Arkansas has led to the development of a rapid PCR assay for the detection of Salmonella in the poultry processing plant. The assay was found to be effective and its reduces both cost and testing time compared to some currently used methods.
Foodborne salmonellosis is a public health concern and poultry and poultry products are often regarded as a primary source of infection, according to Dr Steven C. Ricke and Si Hong Park at the Department of Food Science at the University of Arkansas. They say explain that Salmonella species can be introduced and distributed on carcasses during processing and even low numbers of Salmonella on products can represent a health risk in humans.
The overall objective of their project, which was sponsored by the US Poultry & Egg Association, was to detect and quantify viable Salmonella serovars in poultry carcasses without selective enrichment using multiplex PCR and quantitative PCR (qPCR).
The specific objectives were to:
- optimise both multiplex PCR and qPCR assays for simultaneous detection of Salmonella genus, Salmonella subspecies I, S. enteritidis, S. Heidelberg and S. typhimurium, and
- apply the PCR assays to poultry carcass rinsates for identification of viable Salmonella without enrichment.
It was found that the growth of different Salmonella serovars was most similar and detectable levels occurred much sooner on non-selective Luria Bertani broth than selective enrichment with either RV broth or tetrathionate broth. For PCR assays, using non-selective media that supports the most rapid growth of Salmonella can greatly shorten assay time.
There is indication of competition between serovars during growth. In particular, S. typhimurium exhibited decreased growth in S. Heidelberg (ARI-14) spent media. This could impact current enrichment and most probable number (MPN) enumeration assays and suggests that incubation periods in non-selective media should not be allowed to be extensive as underestimation of certain serovars could occur.
In the development of the PCR assays S. Heidelberg-specific primers that could detect 15 strains isolated from poultry, poultry products and humans were determined.
The multiplex PCR assay using five primer pairs for Salmonella genus (423 bp), Salmonella subspecies I (137 bp), S. enteritidis (171 bp), S. Heidelberg (216 bp) and S. typhimurium (310 bp) was standardised. The quantitative PCR was optimised to detect as low as 46 copies of Salmonella genomic DNA.
It was confirmed that the two PCR assays, when applied to the detection of Salmonella on contaminated chicken breast meat, detected 22 colony-forming units (CFU) per gram after eight hours of non-selective incubation.
Completion of this project provides potential reliable and rapid Salmonella detection for all phases of poultry production, according to Dr Ricke.
Since multiplex PCR can amplify specific DNA sequences and simultaneously discriminate each target strain in a sample, considerable time and costs can be saved.
He added that this method provides a means to design a preventative strategy targeting different stages of processing that includes specific Salmonella serovar quantification analysis as part of the control measures.