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Next generation sequencing-based multigene panel for high throughput detection of food-borne pathogens
- Ferrario, Chiara, Lugli, Gabriele Andrea, Ossiprandi, Maria Cristina, Turroni, Francesca, Milani, Christian, Duranti, Sabrina, Mancabelli, Leonardo, Mangifesta, Marta, Alessandri, Giulia, van Sinderen, Douwe, Ventura, Marco
- International journal of food microbiology 2017 v.256 pp. 20-29
- Campylobacter coli, Campylobacter jejuni, Escherichia coli, Listeria monocytogenes, Shigella sonnei, Staphylococcus aureus, Yersinia enterocolitica, bacteria, food chain, food consumption, food contamination, food matrix, food pathogens, foodborne illness, fruits, oligonucleotides, polymerase chain reaction, ready-to-eat foods, risk, vegetables
- Contamination of food by chemicals or pathogenic bacteria may cause particular illnesses that are linked to food consumption, commonly referred to as foodborne diseases. Bacteria are present in/on various foods products, such as fruits, vegetables and ready-to-eat products. Bacteria that cause foodborne diseases are known as foodborne pathogens (FBPs). Accurate detection methods that are able to reveal the presence of FBPs in food matrices are in constant demand, in order to ensure safe foods with a minimal risk of causing foodborne diseases. Here, a multiplex PCR-based Illumina sequencing method for FBP detection in food matrices was developed. Starting from 25 bacterial targets and 49 selected PCR primer pairs, a primer collection called foodborne pathogen – panel (FPP) consisting of 12 oligonucleotide pairs was developed. The FPP allows a more rapid and reliable identification of FBPs compared to classical cultivation methods. Furthermore, FPP permits sensitive and specific FBP detection in about two days from food sample acquisition to bioinformatics-based identification. The FPP is able to simultaneously identify eight different bacterial pathogens, i.e. Listeria monocytogenes, Campylobacter jejuni, Campylobacter coli, Salmonella enterica subsp. enterica serovar enteritidis, Escherichia coli, Shigella sonnei, Staphylococcus aureus and Yersinia enterocolitica, in a given food matrix at a threshold contamination level of 101cell/g. Moreover, this novel detection method may represent an alternative and/or a complementary approach to PCR-based techniques, which are routinely used for FBP detection, and could be implemented in (parts of) the food chain as a quality check.