One-Day Molecular Detection of <i<Salmonella</i< and <i<Campylobacter</i< in Chicken Meat: A Pilot Study
<i<Salmonella</i< and <i<Campylobacter</i< ssp. are bacterial pathogens responsible for most foodborne infections in EU countries. Poultry serves as a reservoir for these pathogens, and its important role in the meat industry makes it essential to develop a rapid detection as...
Ausführliche Beschreibung
Autor*in: |
Andrea Zendrini [verfasserIn] Valentina Carta [verfasserIn] Virginia Filipello [verfasserIn] Laura Ragni [verfasserIn] Elena Cosciani-Cunico [verfasserIn] Sara Arnaboldi [verfasserIn] Barbara Bertasi [verfasserIn] Niccolò Franceschi [verfasserIn] Paolo Ajmone-Marsan [verfasserIn] Dario De Medici [verfasserIn] Marina Nadia Losio [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2021 |
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Übergeordnetes Werk: |
In: Foods - MDPI AG, 2013, 10(2021), 5, p 1132 |
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Übergeordnetes Werk: |
volume:10 ; year:2021 ; number:5, p 1132 |
Links: |
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DOI / URN: |
10.3390/foods10051132 |
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Katalog-ID: |
DOAJ00343947X |
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10.3390/foods10051132 doi (DE-627)DOAJ00343947X (DE-599)DOAJ510672a7632441f8866fd651eb869c6f DE-627 ger DE-627 rakwb eng TP1-1185 Andrea Zendrini verfasserin aut One-Day Molecular Detection of <i<Salmonella</i< and <i<Campylobacter</i< in Chicken Meat: A Pilot Study 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier <i<Salmonella</i< and <i<Campylobacter</i< ssp. are bacterial pathogens responsible for most foodborne infections in EU countries. Poultry serves as a reservoir for these pathogens, and its important role in the meat industry makes it essential to develop a rapid detection assay able to provide results in one day. Indeed, the rapid identification of foodborne pathogens is an important instrument for the monitoring and prevention of epidemic outbreaks. To date, <i<Salmonella</i< and <i<Campylobacter</i< screening is mainly conducted through molecular methods (PCR or real-time PCR) performed after 18–24 h long enrichments. In this study, we evaluated short enrichments (0, 2, 4, and 6 h) combined with a colorimetric loop-mediated isothermal AMPlification (LAMP) or real-time PCR to detect <i<Salmonella</i< and <i<Campylobacter</i< in poultry meat contaminated at different concentration levels (10<sup<1</sup<, 10<sup<3</sup<, and 10<sup<5</sup< CFU/g). Our results show that real-time PCR allows the detection of <i<Salmonella</i< and <i<Campylobacter</i<, even after shorter enrichment times than prescribed by ISO references; particularly, it detected <i<Salmonella</i< down to 10<sup<1</sup< CFU/g since T0 and <i<Campylobacter</i< from 10<sup<3</sup< CFU/g since T0. Detection with LAMP was comparable to real-time PCR without the requirement of a thermal cycler and with shorter execution times. These characteristics make colorimetric LAMP a valid alternative when one-day results are needed, improving the timely identification of positive meat batches, even in the absence of specialized instrumentation. LAMP <i<Campylobacter</i< <i<Salmonella</i< poultry foodborne diseases Chemical technology Valentina Carta verfasserin aut Virginia Filipello verfasserin aut Laura Ragni verfasserin aut Elena Cosciani-Cunico verfasserin aut Sara Arnaboldi verfasserin aut Barbara Bertasi verfasserin aut Niccolò Franceschi verfasserin aut Paolo Ajmone-Marsan verfasserin aut Dario De Medici verfasserin aut Marina Nadia Losio verfasserin aut In Foods MDPI AG, 2013 10(2021), 5, p 1132 (DE-627)737287632 (DE-600)2704223-6 23048158 nnns volume:10 year:2021 number:5, p 1132 https://doi.org/10.3390/foods10051132 kostenfrei https://doaj.org/article/510672a7632441f8866fd651eb869c6f kostenfrei https://www.mdpi.com/2304-8158/10/5/1132 kostenfrei https://doaj.org/toc/2304-8158 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 10 2021 5, p 1132 |
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10.3390/foods10051132 doi (DE-627)DOAJ00343947X (DE-599)DOAJ510672a7632441f8866fd651eb869c6f DE-627 ger DE-627 rakwb eng TP1-1185 Andrea Zendrini verfasserin aut One-Day Molecular Detection of <i<Salmonella</i< and <i<Campylobacter</i< in Chicken Meat: A Pilot Study 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier <i<Salmonella</i< and <i<Campylobacter</i< ssp. are bacterial pathogens responsible for most foodborne infections in EU countries. Poultry serves as a reservoir for these pathogens, and its important role in the meat industry makes it essential to develop a rapid detection assay able to provide results in one day. Indeed, the rapid identification of foodborne pathogens is an important instrument for the monitoring and prevention of epidemic outbreaks. To date, <i<Salmonella</i< and <i<Campylobacter</i< screening is mainly conducted through molecular methods (PCR or real-time PCR) performed after 18–24 h long enrichments. In this study, we evaluated short enrichments (0, 2, 4, and 6 h) combined with a colorimetric loop-mediated isothermal AMPlification (LAMP) or real-time PCR to detect <i<Salmonella</i< and <i<Campylobacter</i< in poultry meat contaminated at different concentration levels (10<sup<1</sup<, 10<sup<3</sup<, and 10<sup<5</sup< CFU/g). Our results show that real-time PCR allows the detection of <i<Salmonella</i< and <i<Campylobacter</i<, even after shorter enrichment times than prescribed by ISO references; particularly, it detected <i<Salmonella</i< down to 10<sup<1</sup< CFU/g since T0 and <i<Campylobacter</i< from 10<sup<3</sup< CFU/g since T0. Detection with LAMP was comparable to real-time PCR without the requirement of a thermal cycler and with shorter execution times. These characteristics make colorimetric LAMP a valid alternative when one-day results are needed, improving the timely identification of positive meat batches, even in the absence of specialized instrumentation. LAMP <i<Campylobacter</i< <i<Salmonella</i< poultry foodborne diseases Chemical technology Valentina Carta verfasserin aut Virginia Filipello verfasserin aut Laura Ragni verfasserin aut Elena Cosciani-Cunico verfasserin aut Sara Arnaboldi verfasserin aut Barbara Bertasi verfasserin aut Niccolò Franceschi verfasserin aut Paolo Ajmone-Marsan verfasserin aut Dario De Medici verfasserin aut Marina Nadia Losio verfasserin aut In Foods MDPI AG, 2013 10(2021), 5, p 1132 (DE-627)737287632 (DE-600)2704223-6 23048158 nnns volume:10 year:2021 number:5, p 1132 https://doi.org/10.3390/foods10051132 kostenfrei https://doaj.org/article/510672a7632441f8866fd651eb869c6f kostenfrei https://www.mdpi.com/2304-8158/10/5/1132 kostenfrei https://doaj.org/toc/2304-8158 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 10 2021 5, p 1132 |
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10.3390/foods10051132 doi (DE-627)DOAJ00343947X (DE-599)DOAJ510672a7632441f8866fd651eb869c6f DE-627 ger DE-627 rakwb eng TP1-1185 Andrea Zendrini verfasserin aut One-Day Molecular Detection of <i<Salmonella</i< and <i<Campylobacter</i< in Chicken Meat: A Pilot Study 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier <i<Salmonella</i< and <i<Campylobacter</i< ssp. are bacterial pathogens responsible for most foodborne infections in EU countries. Poultry serves as a reservoir for these pathogens, and its important role in the meat industry makes it essential to develop a rapid detection assay able to provide results in one day. Indeed, the rapid identification of foodborne pathogens is an important instrument for the monitoring and prevention of epidemic outbreaks. To date, <i<Salmonella</i< and <i<Campylobacter</i< screening is mainly conducted through molecular methods (PCR or real-time PCR) performed after 18–24 h long enrichments. In this study, we evaluated short enrichments (0, 2, 4, and 6 h) combined with a colorimetric loop-mediated isothermal AMPlification (LAMP) or real-time PCR to detect <i<Salmonella</i< and <i<Campylobacter</i< in poultry meat contaminated at different concentration levels (10<sup<1</sup<, 10<sup<3</sup<, and 10<sup<5</sup< CFU/g). Our results show that real-time PCR allows the detection of <i<Salmonella</i< and <i<Campylobacter</i<, even after shorter enrichment times than prescribed by ISO references; particularly, it detected <i<Salmonella</i< down to 10<sup<1</sup< CFU/g since T0 and <i<Campylobacter</i< from 10<sup<3</sup< CFU/g since T0. Detection with LAMP was comparable to real-time PCR without the requirement of a thermal cycler and with shorter execution times. These characteristics make colorimetric LAMP a valid alternative when one-day results are needed, improving the timely identification of positive meat batches, even in the absence of specialized instrumentation. LAMP <i<Campylobacter</i< <i<Salmonella</i< poultry foodborne diseases Chemical technology Valentina Carta verfasserin aut Virginia Filipello verfasserin aut Laura Ragni verfasserin aut Elena Cosciani-Cunico verfasserin aut Sara Arnaboldi verfasserin aut Barbara Bertasi verfasserin aut Niccolò Franceschi verfasserin aut Paolo Ajmone-Marsan verfasserin aut Dario De Medici verfasserin aut Marina Nadia Losio verfasserin aut In Foods MDPI AG, 2013 10(2021), 5, p 1132 (DE-627)737287632 (DE-600)2704223-6 23048158 nnns volume:10 year:2021 number:5, p 1132 https://doi.org/10.3390/foods10051132 kostenfrei https://doaj.org/article/510672a7632441f8866fd651eb869c6f kostenfrei https://www.mdpi.com/2304-8158/10/5/1132 kostenfrei https://doaj.org/toc/2304-8158 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 10 2021 5, p 1132 |
allfieldsGer |
10.3390/foods10051132 doi (DE-627)DOAJ00343947X (DE-599)DOAJ510672a7632441f8866fd651eb869c6f DE-627 ger DE-627 rakwb eng TP1-1185 Andrea Zendrini verfasserin aut One-Day Molecular Detection of <i<Salmonella</i< and <i<Campylobacter</i< in Chicken Meat: A Pilot Study 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier <i<Salmonella</i< and <i<Campylobacter</i< ssp. are bacterial pathogens responsible for most foodborne infections in EU countries. Poultry serves as a reservoir for these pathogens, and its important role in the meat industry makes it essential to develop a rapid detection assay able to provide results in one day. Indeed, the rapid identification of foodborne pathogens is an important instrument for the monitoring and prevention of epidemic outbreaks. To date, <i<Salmonella</i< and <i<Campylobacter</i< screening is mainly conducted through molecular methods (PCR or real-time PCR) performed after 18–24 h long enrichments. In this study, we evaluated short enrichments (0, 2, 4, and 6 h) combined with a colorimetric loop-mediated isothermal AMPlification (LAMP) or real-time PCR to detect <i<Salmonella</i< and <i<Campylobacter</i< in poultry meat contaminated at different concentration levels (10<sup<1</sup<, 10<sup<3</sup<, and 10<sup<5</sup< CFU/g). Our results show that real-time PCR allows the detection of <i<Salmonella</i< and <i<Campylobacter</i<, even after shorter enrichment times than prescribed by ISO references; particularly, it detected <i<Salmonella</i< down to 10<sup<1</sup< CFU/g since T0 and <i<Campylobacter</i< from 10<sup<3</sup< CFU/g since T0. Detection with LAMP was comparable to real-time PCR without the requirement of a thermal cycler and with shorter execution times. These characteristics make colorimetric LAMP a valid alternative when one-day results are needed, improving the timely identification of positive meat batches, even in the absence of specialized instrumentation. LAMP <i<Campylobacter</i< <i<Salmonella</i< poultry foodborne diseases Chemical technology Valentina Carta verfasserin aut Virginia Filipello verfasserin aut Laura Ragni verfasserin aut Elena Cosciani-Cunico verfasserin aut Sara Arnaboldi verfasserin aut Barbara Bertasi verfasserin aut Niccolò Franceschi verfasserin aut Paolo Ajmone-Marsan verfasserin aut Dario De Medici verfasserin aut Marina Nadia Losio verfasserin aut In Foods MDPI AG, 2013 10(2021), 5, p 1132 (DE-627)737287632 (DE-600)2704223-6 23048158 nnns volume:10 year:2021 number:5, p 1132 https://doi.org/10.3390/foods10051132 kostenfrei https://doaj.org/article/510672a7632441f8866fd651eb869c6f kostenfrei https://www.mdpi.com/2304-8158/10/5/1132 kostenfrei https://doaj.org/toc/2304-8158 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 10 2021 5, p 1132 |
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<i<Salmonella</i< and <i<Campylobacter</i< ssp. are bacterial pathogens responsible for most foodborne infections in EU countries. Poultry serves as a reservoir for these pathogens, and its important role in the meat industry makes it essential to develop a rapid detection assay able to provide results in one day. Indeed, the rapid identification of foodborne pathogens is an important instrument for the monitoring and prevention of epidemic outbreaks. To date, <i<Salmonella</i< and <i<Campylobacter</i< screening is mainly conducted through molecular methods (PCR or real-time PCR) performed after 18–24 h long enrichments. In this study, we evaluated short enrichments (0, 2, 4, and 6 h) combined with a colorimetric loop-mediated isothermal AMPlification (LAMP) or real-time PCR to detect <i<Salmonella</i< and <i<Campylobacter</i< in poultry meat contaminated at different concentration levels (10<sup<1</sup<, 10<sup<3</sup<, and 10<sup<5</sup< CFU/g). Our results show that real-time PCR allows the detection of <i<Salmonella</i< and <i<Campylobacter</i<, even after shorter enrichment times than prescribed by ISO references; particularly, it detected <i<Salmonella</i< down to 10<sup<1</sup< CFU/g since T0 and <i<Campylobacter</i< from 10<sup<3</sup< CFU/g since T0. Detection with LAMP was comparable to real-time PCR without the requirement of a thermal cycler and with shorter execution times. These characteristics make colorimetric LAMP a valid alternative when one-day results are needed, improving the timely identification of positive meat batches, even in the absence of specialized instrumentation. |
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<i<Salmonella</i< and <i<Campylobacter</i< ssp. are bacterial pathogens responsible for most foodborne infections in EU countries. Poultry serves as a reservoir for these pathogens, and its important role in the meat industry makes it essential to develop a rapid detection assay able to provide results in one day. Indeed, the rapid identification of foodborne pathogens is an important instrument for the monitoring and prevention of epidemic outbreaks. To date, <i<Salmonella</i< and <i<Campylobacter</i< screening is mainly conducted through molecular methods (PCR or real-time PCR) performed after 18–24 h long enrichments. In this study, we evaluated short enrichments (0, 2, 4, and 6 h) combined with a colorimetric loop-mediated isothermal AMPlification (LAMP) or real-time PCR to detect <i<Salmonella</i< and <i<Campylobacter</i< in poultry meat contaminated at different concentration levels (10<sup<1</sup<, 10<sup<3</sup<, and 10<sup<5</sup< CFU/g). Our results show that real-time PCR allows the detection of <i<Salmonella</i< and <i<Campylobacter</i<, even after shorter enrichment times than prescribed by ISO references; particularly, it detected <i<Salmonella</i< down to 10<sup<1</sup< CFU/g since T0 and <i<Campylobacter</i< from 10<sup<3</sup< CFU/g since T0. Detection with LAMP was comparable to real-time PCR without the requirement of a thermal cycler and with shorter execution times. These characteristics make colorimetric LAMP a valid alternative when one-day results are needed, improving the timely identification of positive meat batches, even in the absence of specialized instrumentation. |
abstract_unstemmed |
<i<Salmonella</i< and <i<Campylobacter</i< ssp. are bacterial pathogens responsible for most foodborne infections in EU countries. Poultry serves as a reservoir for these pathogens, and its important role in the meat industry makes it essential to develop a rapid detection assay able to provide results in one day. Indeed, the rapid identification of foodborne pathogens is an important instrument for the monitoring and prevention of epidemic outbreaks. To date, <i<Salmonella</i< and <i<Campylobacter</i< screening is mainly conducted through molecular methods (PCR or real-time PCR) performed after 18–24 h long enrichments. In this study, we evaluated short enrichments (0, 2, 4, and 6 h) combined with a colorimetric loop-mediated isothermal AMPlification (LAMP) or real-time PCR to detect <i<Salmonella</i< and <i<Campylobacter</i< in poultry meat contaminated at different concentration levels (10<sup<1</sup<, 10<sup<3</sup<, and 10<sup<5</sup< CFU/g). Our results show that real-time PCR allows the detection of <i<Salmonella</i< and <i<Campylobacter</i<, even after shorter enrichment times than prescribed by ISO references; particularly, it detected <i<Salmonella</i< down to 10<sup<1</sup< CFU/g since T0 and <i<Campylobacter</i< from 10<sup<3</sup< CFU/g since T0. Detection with LAMP was comparable to real-time PCR without the requirement of a thermal cycler and with shorter execution times. These characteristics make colorimetric LAMP a valid alternative when one-day results are needed, improving the timely identification of positive meat batches, even in the absence of specialized instrumentation. |
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5, p 1132 |
title_short |
One-Day Molecular Detection of <i<Salmonella</i< and <i<Campylobacter</i< in Chicken Meat: A Pilot Study |
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https://doi.org/10.3390/foods10051132 https://doaj.org/article/510672a7632441f8866fd651eb869c6f https://www.mdpi.com/2304-8158/10/5/1132 https://doaj.org/toc/2304-8158 |
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Valentina Carta Virginia Filipello Laura Ragni Elena Cosciani-Cunico Sara Arnaboldi Barbara Bertasi Niccolò Franceschi Paolo Ajmone-Marsan Dario De Medici Marina Nadia Losio |
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Valentina Carta Virginia Filipello Laura Ragni Elena Cosciani-Cunico Sara Arnaboldi Barbara Bertasi Niccolò Franceschi Paolo Ajmone-Marsan Dario De Medici Marina Nadia Losio |
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2024-07-03T18:00:27.526Z |
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