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Novel next generation sequencing panel method for the multiple detection and identification of foodborne pathogens in agricultural wastewater

Detecting and identifying the origins of foodborne pathogen outbreaks is a challenging. The Next-Generation Sequencing (NGS) panel method offers a potential solution by enabling efficient screening and identification of various bacteria in one reaction. In this study, new NGS panel primer sets that...

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Autores principales: Park, Dong-Geun, Kwon, Joon-Gi, Ha, Eun-Su, Kang, Byungcheol, Choi, Iseul, Kwak, Jeong-Eun, Choi, Jinho, Lee, Woojung, Kim, Seung Hwan, Kim, Soon Han, Park, Jeongwoong, Lee, Ju-Hoon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10374199/
https://www.ncbi.nlm.nih.gov/pubmed/37520347
http://dx.doi.org/10.3389/fmicb.2023.1179934
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author Park, Dong-Geun
Kwon, Joon-Gi
Ha, Eun-Su
Kang, Byungcheol
Choi, Iseul
Kwak, Jeong-Eun
Choi, Jinho
Lee, Woojung
Kim, Seung Hwan
Kim, Soon Han
Park, Jeongwoong
Lee, Ju-Hoon
author_facet Park, Dong-Geun
Kwon, Joon-Gi
Ha, Eun-Su
Kang, Byungcheol
Choi, Iseul
Kwak, Jeong-Eun
Choi, Jinho
Lee, Woojung
Kim, Seung Hwan
Kim, Soon Han
Park, Jeongwoong
Lee, Ju-Hoon
author_sort Park, Dong-Geun
collection PubMed
description Detecting and identifying the origins of foodborne pathogen outbreaks is a challenging. The Next-Generation Sequencing (NGS) panel method offers a potential solution by enabling efficient screening and identification of various bacteria in one reaction. In this study, new NGS panel primer sets that target 18 specific virulence factor genes from six target pathogens (Bacillus cereus, Yersinia enterocolitica, Staphylococcus aureus, Vibrio cholerae, Vibrio parahaemolyticus, and Vibrio vulnificus) were developed and optimized. The primer sets were validated for specificity and selectivity through singleplex PCR, confirming the expected amplicon size. Crosscheck and multiplex PCR showed no interference in the primer set or pathogenic DNA mixture. The NGS panel analysis of spiked water samples detected all 18 target genes in a single reaction, with pathogen concentrations ranging from 10(8) to 10(5) colony-forming units (CFUs) per target pathogen. Notably, the total sequence read counts from the virulence factor genes showed a positive association with the CFUs per target pathogen. However, the method exhibited relatively low sensitivity and occasional false positive results at low pathogen concentrations of 10(5) CFUs. To validate the detection and identification results, two sets of quantitative real-time PCR (qPCR) analyses were independently performed on the same spiked water samples, yielding almost the same efficiency and specificity compared to the NGS panel analysis. Comparative statistical analysis and Spearman correlation analysis further supported the similarity of the results by showing a negative association between the NGS panel sequence read counts and qPCR cycle threshold (Ct) values. To enhance NGS panel analysis for better detection, optimization of primer sets and real-time NGS sequencing technology are essential. Nonetheless, this study provides valuable insights into applying NGS panel analysis for multiple foodborne pathogen detection, emphasizing its potential in ensuring food safety.
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spelling pubmed-103741992023-07-28 Novel next generation sequencing panel method for the multiple detection and identification of foodborne pathogens in agricultural wastewater Park, Dong-Geun Kwon, Joon-Gi Ha, Eun-Su Kang, Byungcheol Choi, Iseul Kwak, Jeong-Eun Choi, Jinho Lee, Woojung Kim, Seung Hwan Kim, Soon Han Park, Jeongwoong Lee, Ju-Hoon Front Microbiol Microbiology Detecting and identifying the origins of foodborne pathogen outbreaks is a challenging. The Next-Generation Sequencing (NGS) panel method offers a potential solution by enabling efficient screening and identification of various bacteria in one reaction. In this study, new NGS panel primer sets that target 18 specific virulence factor genes from six target pathogens (Bacillus cereus, Yersinia enterocolitica, Staphylococcus aureus, Vibrio cholerae, Vibrio parahaemolyticus, and Vibrio vulnificus) were developed and optimized. The primer sets were validated for specificity and selectivity through singleplex PCR, confirming the expected amplicon size. Crosscheck and multiplex PCR showed no interference in the primer set or pathogenic DNA mixture. The NGS panel analysis of spiked water samples detected all 18 target genes in a single reaction, with pathogen concentrations ranging from 10(8) to 10(5) colony-forming units (CFUs) per target pathogen. Notably, the total sequence read counts from the virulence factor genes showed a positive association with the CFUs per target pathogen. However, the method exhibited relatively low sensitivity and occasional false positive results at low pathogen concentrations of 10(5) CFUs. To validate the detection and identification results, two sets of quantitative real-time PCR (qPCR) analyses were independently performed on the same spiked water samples, yielding almost the same efficiency and specificity compared to the NGS panel analysis. Comparative statistical analysis and Spearman correlation analysis further supported the similarity of the results by showing a negative association between the NGS panel sequence read counts and qPCR cycle threshold (Ct) values. To enhance NGS panel analysis for better detection, optimization of primer sets and real-time NGS sequencing technology are essential. Nonetheless, this study provides valuable insights into applying NGS panel analysis for multiple foodborne pathogen detection, emphasizing its potential in ensuring food safety. Frontiers Media S.A. 2023-07-13 /pmc/articles/PMC10374199/ /pubmed/37520347 http://dx.doi.org/10.3389/fmicb.2023.1179934 Text en Copyright © 2023 Park, Kwon, Ha, Kang, Choi, Kwak, Choi, Lee, Kim, Kim, Park and Lee. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Park, Dong-Geun
Kwon, Joon-Gi
Ha, Eun-Su
Kang, Byungcheol
Choi, Iseul
Kwak, Jeong-Eun
Choi, Jinho
Lee, Woojung
Kim, Seung Hwan
Kim, Soon Han
Park, Jeongwoong
Lee, Ju-Hoon
Novel next generation sequencing panel method for the multiple detection and identification of foodborne pathogens in agricultural wastewater
title Novel next generation sequencing panel method for the multiple detection and identification of foodborne pathogens in agricultural wastewater
title_full Novel next generation sequencing panel method for the multiple detection and identification of foodborne pathogens in agricultural wastewater
title_fullStr Novel next generation sequencing panel method for the multiple detection and identification of foodborne pathogens in agricultural wastewater
title_full_unstemmed Novel next generation sequencing panel method for the multiple detection and identification of foodborne pathogens in agricultural wastewater
title_short Novel next generation sequencing panel method for the multiple detection and identification of foodborne pathogens in agricultural wastewater
title_sort novel next generation sequencing panel method for the multiple detection and identification of foodborne pathogens in agricultural wastewater
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10374199/
https://www.ncbi.nlm.nih.gov/pubmed/37520347
http://dx.doi.org/10.3389/fmicb.2023.1179934
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