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Screening for fecal carriage of MCR-producing Enterobacteriaceae in healthy humans and primary care patients

BACKGROUND: The extent of the occurrence of the plasmid-encoded colistin resistance genes mcr-1 and mcr-2 among humans is currently sparsely studied in Western Europe. OBJECTIVES: To determine the occurrence of MCR-producing Enterobacteriaceae in fecal samples of healthy humans with high occupationa...

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Autores principales: Zurfluh, Katrin, Stephan, Roger, Widmer, Andreas, Poirel, Laurent, Nordmann, Patrice, Nüesch, Hans-Jakob, Hächler, Herbert, Nüesch-Inderbinen, Magdalena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5351167/
https://www.ncbi.nlm.nih.gov/pubmed/28316780
http://dx.doi.org/10.1186/s13756-017-0186-z
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author Zurfluh, Katrin
Stephan, Roger
Widmer, Andreas
Poirel, Laurent
Nordmann, Patrice
Nüesch, Hans-Jakob
Hächler, Herbert
Nüesch-Inderbinen, Magdalena
author_facet Zurfluh, Katrin
Stephan, Roger
Widmer, Andreas
Poirel, Laurent
Nordmann, Patrice
Nüesch, Hans-Jakob
Hächler, Herbert
Nüesch-Inderbinen, Magdalena
author_sort Zurfluh, Katrin
collection PubMed
description BACKGROUND: The extent of the occurrence of the plasmid-encoded colistin resistance genes mcr-1 and mcr-2 among humans is currently sparsely studied in Western Europe. OBJECTIVES: To determine the occurrence of MCR-producing Enterobacteriaceae in fecal samples of healthy humans with high occupational exposure to food and primary care patients in Switzerland. METHODS: Stool samples from 1091 healthy individuals and fecal swabs from 53 primary care patients were screened for polymyxin-resistant Enterobacteriaceae using LB agar containing 4 mg/L colistin. Minimal inhibitory concentrations (MICs) of colistin were determined for non-intrinsic colistin-resistant isolates. Isolates were screened by PCR for the presence of mcr-1 and mcr-2 genes. RESULTS: The fecal carriage rate of colistin resistant (MIC value >2 mg/l) Enterobacteriaceae was 1.5% for healthy people and 3.8% for primary care patients. Isolates included Hafnia alvei (n = 9), Escherichia coli (n = 3), Enterobacter cloacae (n = 4), Klebsiella pneumoniae (n = 1) and Raoultella ornithinolytica (n = 1). None of the isolates harbored the mcr-1 or mcr-2 genes. CONCLUSIONS: There is no evidence for the presence of MCR-producers in the fecal flora of healthy people or primary care patients. Therefore, the risk of transfer of mcr genes from animals, food or the environment to humans is likely to be low in Switzerland.
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spelling pubmed-53511672017-03-17 Screening for fecal carriage of MCR-producing Enterobacteriaceae in healthy humans and primary care patients Zurfluh, Katrin Stephan, Roger Widmer, Andreas Poirel, Laurent Nordmann, Patrice Nüesch, Hans-Jakob Hächler, Herbert Nüesch-Inderbinen, Magdalena Antimicrob Resist Infect Control Short Report BACKGROUND: The extent of the occurrence of the plasmid-encoded colistin resistance genes mcr-1 and mcr-2 among humans is currently sparsely studied in Western Europe. OBJECTIVES: To determine the occurrence of MCR-producing Enterobacteriaceae in fecal samples of healthy humans with high occupational exposure to food and primary care patients in Switzerland. METHODS: Stool samples from 1091 healthy individuals and fecal swabs from 53 primary care patients were screened for polymyxin-resistant Enterobacteriaceae using LB agar containing 4 mg/L colistin. Minimal inhibitory concentrations (MICs) of colistin were determined for non-intrinsic colistin-resistant isolates. Isolates were screened by PCR for the presence of mcr-1 and mcr-2 genes. RESULTS: The fecal carriage rate of colistin resistant (MIC value >2 mg/l) Enterobacteriaceae was 1.5% for healthy people and 3.8% for primary care patients. Isolates included Hafnia alvei (n = 9), Escherichia coli (n = 3), Enterobacter cloacae (n = 4), Klebsiella pneumoniae (n = 1) and Raoultella ornithinolytica (n = 1). None of the isolates harbored the mcr-1 or mcr-2 genes. CONCLUSIONS: There is no evidence for the presence of MCR-producers in the fecal flora of healthy people or primary care patients. Therefore, the risk of transfer of mcr genes from animals, food or the environment to humans is likely to be low in Switzerland. BioMed Central 2017-03-14 /pmc/articles/PMC5351167/ /pubmed/28316780 http://dx.doi.org/10.1186/s13756-017-0186-z Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Short Report
Zurfluh, Katrin
Stephan, Roger
Widmer, Andreas
Poirel, Laurent
Nordmann, Patrice
Nüesch, Hans-Jakob
Hächler, Herbert
Nüesch-Inderbinen, Magdalena
Screening for fecal carriage of MCR-producing Enterobacteriaceae in healthy humans and primary care patients
title Screening for fecal carriage of MCR-producing Enterobacteriaceae in healthy humans and primary care patients
title_full Screening for fecal carriage of MCR-producing Enterobacteriaceae in healthy humans and primary care patients
title_fullStr Screening for fecal carriage of MCR-producing Enterobacteriaceae in healthy humans and primary care patients
title_full_unstemmed Screening for fecal carriage of MCR-producing Enterobacteriaceae in healthy humans and primary care patients
title_short Screening for fecal carriage of MCR-producing Enterobacteriaceae in healthy humans and primary care patients
title_sort screening for fecal carriage of mcr-producing enterobacteriaceae in healthy humans and primary care patients
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5351167/
https://www.ncbi.nlm.nih.gov/pubmed/28316780
http://dx.doi.org/10.1186/s13756-017-0186-z
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