Cargando…
Evaluation of a Modified Cefsulodin-Irgasan-Novobiocin Agar for Isolation of Yersinia spp
Y. enterocolitica and Y. pseudotuberculosis are important food borne pathogens. However, the presence of competitive microbiota makes the isolation of Y. enterocolitica and Y. pseudotuberculosis from naturally contaminated foods difficult. We attempted to evaluate the performance of a modified Cefsu...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4149559/ https://www.ncbi.nlm.nih.gov/pubmed/25170941 http://dx.doi.org/10.1371/journal.pone.0106329 |
_version_ | 1782332782946549760 |
---|---|
author | Tan, Lai Kuan Ooi, Peck Toung Carniel, Elisabeth Thong, Kwai Lin |
author_facet | Tan, Lai Kuan Ooi, Peck Toung Carniel, Elisabeth Thong, Kwai Lin |
author_sort | Tan, Lai Kuan |
collection | PubMed |
description | Y. enterocolitica and Y. pseudotuberculosis are important food borne pathogens. However, the presence of competitive microbiota makes the isolation of Y. enterocolitica and Y. pseudotuberculosis from naturally contaminated foods difficult. We attempted to evaluate the performance of a modified Cefsulodin-Irgasan-Novobiocin (CIN) agar in the differentiation of Y. enterocolitica from non-Yersinia species, particularly the natural intestinal microbiota. The modified CIN enabled the growth of Y. enterocolitica colonies with the same efficiency as CIN and Luria-Bertani agar. The detection limits of the modified CIN for Y. enterocolitica in culture medium (10 cfu/ml) and in artificially contaminated pork (10(4) cfu/ml) were also comparable to those of CIN. However, the modified CIN provided a better discrimination of Yersinia colonies from other bacteria exhibiting Yersinia-like colonies on CIN (H(2)S-producing Citrobacter freundii, C. braakii, Enterobacter cloacae, Aeromonas hydrophila, Providencia rettgeri, and Morganella morganii). The modified CIN exhibited a higher recovery rate of Y. enterocolitica from artificially prepared bacterial cultures and naturally contaminated samples compared with CIN. Our results thus demonstrated that the use of modified CIN may be a valuable means to increase the recovery rate of food borne Yersinia from natural samples, which are usually contaminated by multiple types of bacteria. |
format | Online Article Text |
id | pubmed-4149559 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-41495592014-09-03 Evaluation of a Modified Cefsulodin-Irgasan-Novobiocin Agar for Isolation of Yersinia spp Tan, Lai Kuan Ooi, Peck Toung Carniel, Elisabeth Thong, Kwai Lin PLoS One Research Article Y. enterocolitica and Y. pseudotuberculosis are important food borne pathogens. However, the presence of competitive microbiota makes the isolation of Y. enterocolitica and Y. pseudotuberculosis from naturally contaminated foods difficult. We attempted to evaluate the performance of a modified Cefsulodin-Irgasan-Novobiocin (CIN) agar in the differentiation of Y. enterocolitica from non-Yersinia species, particularly the natural intestinal microbiota. The modified CIN enabled the growth of Y. enterocolitica colonies with the same efficiency as CIN and Luria-Bertani agar. The detection limits of the modified CIN for Y. enterocolitica in culture medium (10 cfu/ml) and in artificially contaminated pork (10(4) cfu/ml) were also comparable to those of CIN. However, the modified CIN provided a better discrimination of Yersinia colonies from other bacteria exhibiting Yersinia-like colonies on CIN (H(2)S-producing Citrobacter freundii, C. braakii, Enterobacter cloacae, Aeromonas hydrophila, Providencia rettgeri, and Morganella morganii). The modified CIN exhibited a higher recovery rate of Y. enterocolitica from artificially prepared bacterial cultures and naturally contaminated samples compared with CIN. Our results thus demonstrated that the use of modified CIN may be a valuable means to increase the recovery rate of food borne Yersinia from natural samples, which are usually contaminated by multiple types of bacteria. Public Library of Science 2014-08-29 /pmc/articles/PMC4149559/ /pubmed/25170941 http://dx.doi.org/10.1371/journal.pone.0106329 Text en © 2014 Tan et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Tan, Lai Kuan Ooi, Peck Toung Carniel, Elisabeth Thong, Kwai Lin Evaluation of a Modified Cefsulodin-Irgasan-Novobiocin Agar for Isolation of Yersinia spp |
title | Evaluation of a Modified Cefsulodin-Irgasan-Novobiocin Agar for Isolation of Yersinia spp |
title_full | Evaluation of a Modified Cefsulodin-Irgasan-Novobiocin Agar for Isolation of Yersinia spp |
title_fullStr | Evaluation of a Modified Cefsulodin-Irgasan-Novobiocin Agar for Isolation of Yersinia spp |
title_full_unstemmed | Evaluation of a Modified Cefsulodin-Irgasan-Novobiocin Agar for Isolation of Yersinia spp |
title_short | Evaluation of a Modified Cefsulodin-Irgasan-Novobiocin Agar for Isolation of Yersinia spp |
title_sort | evaluation of a modified cefsulodin-irgasan-novobiocin agar for isolation of yersinia spp |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4149559/ https://www.ncbi.nlm.nih.gov/pubmed/25170941 http://dx.doi.org/10.1371/journal.pone.0106329 |
work_keys_str_mv | AT tanlaikuan evaluationofamodifiedcefsulodinirgasannovobiocinagarforisolationofyersiniaspp AT ooipecktoung evaluationofamodifiedcefsulodinirgasannovobiocinagarforisolationofyersiniaspp AT carnielelisabeth evaluationofamodifiedcefsulodinirgasannovobiocinagarforisolationofyersiniaspp AT thongkwailin evaluationofamodifiedcefsulodinirgasannovobiocinagarforisolationofyersiniaspp |