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Bacteriophage-Mediated Modulation of Bacterial Competition during Selective Enrichment of Campylobacter

Selective media using antimicrobial supplements generate unique microbial ecology to facilitate bacterial isolation. However, antibiotic-resistant bacteria indigenous to samples can interfere with the isolation process using selective media. Recent studies showed that extended-spectrum beta-lactamas...

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Autores principales: Kim, Jinshil, Hur, Jeong In, Ryu, Sangryeol, Jeon, Byeonghwa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8672905/
https://www.ncbi.nlm.nih.gov/pubmed/34908437
http://dx.doi.org/10.1128/Spectrum.01703-21
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author Kim, Jinshil
Hur, Jeong In
Ryu, Sangryeol
Jeon, Byeonghwa
author_facet Kim, Jinshil
Hur, Jeong In
Ryu, Sangryeol
Jeon, Byeonghwa
author_sort Kim, Jinshil
collection PubMed
description Selective media using antimicrobial supplements generate unique microbial ecology to facilitate bacterial isolation. However, antibiotic-resistant bacteria indigenous to samples can interfere with the isolation process using selective media. Recent studies showed that extended-spectrum beta-lactamase (ESBL)-producing Escherichia coli is highly prevalent on retail raw chicken and compromises the efficacy of Campylobacter isolation because ESBL-producing E. coli are resistant to antimicrobial supplements in Campylobacter-selective media and outgrows Campylobacter. The objective of this study was to improve Campylobacter isolation by inhibiting the growth of ESBL-producing E. coli using bacteriophages (phages). The supplementation of Campylobacter-selective media with E. coli phages reduced the level of ESBL-producing E. coli during the enrichment step. When E. coli phages were combined with the antimicrobial supplements of Campylobacter-selective media, antimicrobial synergy was observed, particularly with rifampicin, an antibiotic used in Preston medium. Although the same materials (i.e., phages and selective media) were used, the sequence of combining the materials markedly influenced the inhibition of ESBL-producing E. coli and the isolation of Campylobacter. These findings indicated that the modulation of microbial competition at the enrichment step was critical to the successful isolation of fastidious bacteria and that phages can be utilized to facilitate the selective enrichment of target bacteria by inhibiting their competitive bacteria. IMPORTANCE Phages are promising antimicrobial alternatives. In this study, we first demonstrated that phages can be used to facilitate selective isolation of fastidious bacteria that are prone to be outgrown by bacterial competitors during isolation. The effectiveness of a phage-based isolation method was primarily dependent on the antimicrobial synergy between phages and antibiotics used in selective media. The same approach could be applied to the development of isolation methods for other fastidious bacteria.
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spelling pubmed-86729052021-12-16 Bacteriophage-Mediated Modulation of Bacterial Competition during Selective Enrichment of Campylobacter Kim, Jinshil Hur, Jeong In Ryu, Sangryeol Jeon, Byeonghwa Microbiol Spectr Research Article Selective media using antimicrobial supplements generate unique microbial ecology to facilitate bacterial isolation. However, antibiotic-resistant bacteria indigenous to samples can interfere with the isolation process using selective media. Recent studies showed that extended-spectrum beta-lactamase (ESBL)-producing Escherichia coli is highly prevalent on retail raw chicken and compromises the efficacy of Campylobacter isolation because ESBL-producing E. coli are resistant to antimicrobial supplements in Campylobacter-selective media and outgrows Campylobacter. The objective of this study was to improve Campylobacter isolation by inhibiting the growth of ESBL-producing E. coli using bacteriophages (phages). The supplementation of Campylobacter-selective media with E. coli phages reduced the level of ESBL-producing E. coli during the enrichment step. When E. coli phages were combined with the antimicrobial supplements of Campylobacter-selective media, antimicrobial synergy was observed, particularly with rifampicin, an antibiotic used in Preston medium. Although the same materials (i.e., phages and selective media) were used, the sequence of combining the materials markedly influenced the inhibition of ESBL-producing E. coli and the isolation of Campylobacter. These findings indicated that the modulation of microbial competition at the enrichment step was critical to the successful isolation of fastidious bacteria and that phages can be utilized to facilitate the selective enrichment of target bacteria by inhibiting their competitive bacteria. IMPORTANCE Phages are promising antimicrobial alternatives. In this study, we first demonstrated that phages can be used to facilitate selective isolation of fastidious bacteria that are prone to be outgrown by bacterial competitors during isolation. The effectiveness of a phage-based isolation method was primarily dependent on the antimicrobial synergy between phages and antibiotics used in selective media. The same approach could be applied to the development of isolation methods for other fastidious bacteria. American Society for Microbiology 2021-12-15 /pmc/articles/PMC8672905/ /pubmed/34908437 http://dx.doi.org/10.1128/Spectrum.01703-21 Text en Copyright © 2021 Kim et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Kim, Jinshil
Hur, Jeong In
Ryu, Sangryeol
Jeon, Byeonghwa
Bacteriophage-Mediated Modulation of Bacterial Competition during Selective Enrichment of Campylobacter
title Bacteriophage-Mediated Modulation of Bacterial Competition during Selective Enrichment of Campylobacter
title_full Bacteriophage-Mediated Modulation of Bacterial Competition during Selective Enrichment of Campylobacter
title_fullStr Bacteriophage-Mediated Modulation of Bacterial Competition during Selective Enrichment of Campylobacter
title_full_unstemmed Bacteriophage-Mediated Modulation of Bacterial Competition during Selective Enrichment of Campylobacter
title_short Bacteriophage-Mediated Modulation of Bacterial Competition during Selective Enrichment of Campylobacter
title_sort bacteriophage-mediated modulation of bacterial competition during selective enrichment of campylobacter
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8672905/
https://www.ncbi.nlm.nih.gov/pubmed/34908437
http://dx.doi.org/10.1128/Spectrum.01703-21
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