DNA-based bead array technology for simultaneous identification of eleven foodborne pathogens in chicken meat

© 2019 Elsevier Ltd A DNA-based bead array method was successfully developed to simultaneously discriminate 11 pathogens namely Listeria grayi, L. innocua, L. ivanovii, L. monocytogenes, L. seeligeri, L. welshimeri, Escherichia coli, E. coli O157:H7, Staphylococcus aureus, methicillin-resistant S. a...

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Main Authors: Ratthaphol Charlermroj, Manlika Makornwattana, Sudtida Phuengwas, Jomkhwan Meerak, Duangporn Pichpol, Nitsara Karoonuthaisiri
Format: Journal
Published: 2019
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http://cmuir.cmu.ac.th/jspui/handle/6653943832/63517
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Institution: Chiang Mai University
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spelling th-cmuir.6653943832-635172019-03-18T02:20:55Z DNA-based bead array technology for simultaneous identification of eleven foodborne pathogens in chicken meat Ratthaphol Charlermroj Manlika Makornwattana Sudtida Phuengwas Jomkhwan Meerak Duangporn Pichpol Nitsara Karoonuthaisiri Agricultural and Biological Sciences Biochemistry, Genetics and Molecular Biology © 2019 Elsevier Ltd A DNA-based bead array method was successfully developed to simultaneously discriminate 11 pathogens namely Listeria grayi, L. innocua, L. ivanovii, L. monocytogenes, L. seeligeri, L. welshimeri, Escherichia coli, E. coli O157:H7, Staphylococcus aureus, methicillin-resistant S. aureus, and Salmonella spp. for multi purposes: food safety, hygiene indication, antibiotic resistance treatment. The bead array technology is based on fluorescent-barcoded paramagnetic beads with unique 24 oligonucleotide (anti-TAG) sequences which can capture biotinylated PCR product with complementary TAG sequence. R-phycoerythrin labeled streptavidin is used to report the presence of the biotinylated PCR products. After optimizing assay conditions, amplification and biotinylation steps can be performed in a single reaction without further purification before hybridization between the biotinylated TAG products and anti-TAG beads. To ensure that the developed method could provide accurate testing with the real food sample, a total of 311 bacterial isolates from 194 chicken meat samples were tested. The results were compared with those from the conventional ISO methods and revealed the relative accuracy, relative specificity, and relative sensitivity of 96%, 100%, and 95%, respectively. Therefore, the developed method was demonstrated to be useful to distinguish 11 bacteria species at the same time with high accuracy, specificity, and sensitivity. 2019-03-18T02:20:11Z 2019-03-18T02:20:11Z 2019-07-01 Journal 09567135 2-s2.0-85062684506 10.1016/j.foodcont.2019.02.014 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85062684506&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/63517
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Agricultural and Biological Sciences
Biochemistry, Genetics and Molecular Biology
spellingShingle Agricultural and Biological Sciences
Biochemistry, Genetics and Molecular Biology
Ratthaphol Charlermroj
Manlika Makornwattana
Sudtida Phuengwas
Jomkhwan Meerak
Duangporn Pichpol
Nitsara Karoonuthaisiri
DNA-based bead array technology for simultaneous identification of eleven foodborne pathogens in chicken meat
description © 2019 Elsevier Ltd A DNA-based bead array method was successfully developed to simultaneously discriminate 11 pathogens namely Listeria grayi, L. innocua, L. ivanovii, L. monocytogenes, L. seeligeri, L. welshimeri, Escherichia coli, E. coli O157:H7, Staphylococcus aureus, methicillin-resistant S. aureus, and Salmonella spp. for multi purposes: food safety, hygiene indication, antibiotic resistance treatment. The bead array technology is based on fluorescent-barcoded paramagnetic beads with unique 24 oligonucleotide (anti-TAG) sequences which can capture biotinylated PCR product with complementary TAG sequence. R-phycoerythrin labeled streptavidin is used to report the presence of the biotinylated PCR products. After optimizing assay conditions, amplification and biotinylation steps can be performed in a single reaction without further purification before hybridization between the biotinylated TAG products and anti-TAG beads. To ensure that the developed method could provide accurate testing with the real food sample, a total of 311 bacterial isolates from 194 chicken meat samples were tested. The results were compared with those from the conventional ISO methods and revealed the relative accuracy, relative specificity, and relative sensitivity of 96%, 100%, and 95%, respectively. Therefore, the developed method was demonstrated to be useful to distinguish 11 bacteria species at the same time with high accuracy, specificity, and sensitivity.
format Journal
author Ratthaphol Charlermroj
Manlika Makornwattana
Sudtida Phuengwas
Jomkhwan Meerak
Duangporn Pichpol
Nitsara Karoonuthaisiri
author_facet Ratthaphol Charlermroj
Manlika Makornwattana
Sudtida Phuengwas
Jomkhwan Meerak
Duangporn Pichpol
Nitsara Karoonuthaisiri
author_sort Ratthaphol Charlermroj
title DNA-based bead array technology for simultaneous identification of eleven foodborne pathogens in chicken meat
title_short DNA-based bead array technology for simultaneous identification of eleven foodborne pathogens in chicken meat
title_full DNA-based bead array technology for simultaneous identification of eleven foodborne pathogens in chicken meat
title_fullStr DNA-based bead array technology for simultaneous identification of eleven foodborne pathogens in chicken meat
title_full_unstemmed DNA-based bead array technology for simultaneous identification of eleven foodborne pathogens in chicken meat
title_sort dna-based bead array technology for simultaneous identification of eleven foodborne pathogens in chicken meat
publishDate 2019
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85062684506&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/63517
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