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An Improved Culture Method for Selective Isolation of Campylobacter jejuni from Wastewater

Campylobacter jejuni is one of the leading foodborne pathogens worldwide. C. jejuni is isolated from a wide range of foods, domestic animals, wildlife, and environmental sources. The currently available culture-based isolation methods are not highly effective for wastewater samples due to the low nu...

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Autores principales: Kim, Jinyong, Oh, Euna, Banting, Graham S., Braithwaite, Shannon, Chui, Linda, Ashbolt, Nicholas J., Neumann, Norman F., Jeon, Byeonghwa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4999441/
https://www.ncbi.nlm.nih.gov/pubmed/27617011
http://dx.doi.org/10.3389/fmicb.2016.01345
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author Kim, Jinyong
Oh, Euna
Banting, Graham S.
Braithwaite, Shannon
Chui, Linda
Ashbolt, Nicholas J.
Neumann, Norman F.
Jeon, Byeonghwa
author_facet Kim, Jinyong
Oh, Euna
Banting, Graham S.
Braithwaite, Shannon
Chui, Linda
Ashbolt, Nicholas J.
Neumann, Norman F.
Jeon, Byeonghwa
author_sort Kim, Jinyong
collection PubMed
description Campylobacter jejuni is one of the leading foodborne pathogens worldwide. C. jejuni is isolated from a wide range of foods, domestic animals, wildlife, and environmental sources. The currently available culture-based isolation methods are not highly effective for wastewater samples due to the low number of C. jejuni in the midst of competing bacteria. To detect and isolate C. jejuni from wastewater samples, in this study, we evaluated a few different enrichment conditions using five different antibiotics (i.e., cefoperazone, vancomycin, trimethoprim, polymyxin B, and rifampicin), to which C. jejuni is intrinsically resistant. The selectivity of each enrichment condition was measured with C(t) value using quantitative real-time PCR, and multiplex PCR to determine Campylobacter species. In addition, the efficacy of Campylobacter isolation on different culture media after selective enrichment was examined by growing on Bolton and Preston agar plates. The addition of polymyxin B, rifampicin, or both to the Bolton selective supplements enhanced the selective isolation of C. jejuni. The results of 16S rDNA sequencing also revealed that Enterococcus spp. and Pseudomonas aeruginosa are major competing bacteria in the enrichment conditions. Although it is known to be difficult to isolate Campylobacter from samples with heavy contamination, this study well exhibited that the manipulation of antibiotic selective pressure improves the isolation efficiency of fastidious Campylobacter from wastewater.
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spelling pubmed-49994412016-09-09 An Improved Culture Method for Selective Isolation of Campylobacter jejuni from Wastewater Kim, Jinyong Oh, Euna Banting, Graham S. Braithwaite, Shannon Chui, Linda Ashbolt, Nicholas J. Neumann, Norman F. Jeon, Byeonghwa Front Microbiol Microbiology Campylobacter jejuni is one of the leading foodborne pathogens worldwide. C. jejuni is isolated from a wide range of foods, domestic animals, wildlife, and environmental sources. The currently available culture-based isolation methods are not highly effective for wastewater samples due to the low number of C. jejuni in the midst of competing bacteria. To detect and isolate C. jejuni from wastewater samples, in this study, we evaluated a few different enrichment conditions using five different antibiotics (i.e., cefoperazone, vancomycin, trimethoprim, polymyxin B, and rifampicin), to which C. jejuni is intrinsically resistant. The selectivity of each enrichment condition was measured with C(t) value using quantitative real-time PCR, and multiplex PCR to determine Campylobacter species. In addition, the efficacy of Campylobacter isolation on different culture media after selective enrichment was examined by growing on Bolton and Preston agar plates. The addition of polymyxin B, rifampicin, or both to the Bolton selective supplements enhanced the selective isolation of C. jejuni. The results of 16S rDNA sequencing also revealed that Enterococcus spp. and Pseudomonas aeruginosa are major competing bacteria in the enrichment conditions. Although it is known to be difficult to isolate Campylobacter from samples with heavy contamination, this study well exhibited that the manipulation of antibiotic selective pressure improves the isolation efficiency of fastidious Campylobacter from wastewater. Frontiers Media S.A. 2016-08-26 /pmc/articles/PMC4999441/ /pubmed/27617011 http://dx.doi.org/10.3389/fmicb.2016.01345 Text en Copyright © 2016 Kim, Oh, Banting, Braithwaite, Chui, Ashbolt, Neumann and Jeon. http://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) or licensor 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
Kim, Jinyong
Oh, Euna
Banting, Graham S.
Braithwaite, Shannon
Chui, Linda
Ashbolt, Nicholas J.
Neumann, Norman F.
Jeon, Byeonghwa
An Improved Culture Method for Selective Isolation of Campylobacter jejuni from Wastewater
title An Improved Culture Method for Selective Isolation of Campylobacter jejuni from Wastewater
title_full An Improved Culture Method for Selective Isolation of Campylobacter jejuni from Wastewater
title_fullStr An Improved Culture Method for Selective Isolation of Campylobacter jejuni from Wastewater
title_full_unstemmed An Improved Culture Method for Selective Isolation of Campylobacter jejuni from Wastewater
title_short An Improved Culture Method for Selective Isolation of Campylobacter jejuni from Wastewater
title_sort improved culture method for selective isolation of campylobacter jejuni from wastewater
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4999441/
https://www.ncbi.nlm.nih.gov/pubmed/27617011
http://dx.doi.org/10.3389/fmicb.2016.01345
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