Phylogenetic, virulence and antibiotic resistance characteristics of commensal strain populations of Escherichia coli from community subjects in the Paris area in 2010 and evolution over 30 years
It is important to study commensal populations of Escherichia coli because they appear to be the reservoir of both extra-intestinal pathogenic E. coli and antibiotic resistant strains of E. coli. We studied 279 dominant faecal strains of E. coli from 243 adults living in the community in the Paris a...
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Published in | Microbiology (Society for General Microbiology) Vol. 162; no. 4; pp. 642 - 650 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Microbiology Society
01.04.2016
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Subjects | |
Online Access | Get full text |
ISSN | 1350-0872 1465-2080 |
DOI | 10.1099/mic.0.000242 |
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Abstract | It is important to study commensal populations of Escherichia coli because they appear to be the reservoir of both extra-intestinal pathogenic E. coli and antibiotic resistant strains of E. coli. We studied 279 dominant faecal strains of E. coli from 243 adults living in the community in the Paris area in 2010. The phylogenetic group and subgroup [sequence type complex (STc)] of the isolates and the presence of 20 virulence genes were determined by PCR assays. The O-types and resistance to 18 antibiotics were assessed phenotypically. The B2 group was the most frequently recovered (34.0 %), followed by the A group (28.7 %), and other groups were more rare. The most prevalent B2 subgroups were II (STc73), IV (STc141), IX (STc95) and I (STc131), with 22.1, 21.1, 16.8 and 13.7 %, respectively, of the B2 group strains. Virulence factors (VFs) were more common in B2 group than other strains. One or more resistances were found in 125 strains (44.8 % of the collection) but only six (2.2 % of the collection) were multiresistant; no extended-spectrum beta-lactamase-producing strain was isolated. The C phylogroup and clonal group A strains were the most resistant. No trade-off between virulence and resistance was evidenced. We compared these strains with collections of strains gathered under the same conditions 30 and 10 years ago. There has been a parallel and linked increase in the frequency of B2 group strains (from 9.4 % in 1980, to 22.7 % in 2000 and 34.0 % in 2010) and of VFs. Antibiotic resistance also increased, from 22.6 % of strains resistant to at least one antibiotic in 1980, to 31.8 % in 2000 and 44.8 % in 2010; resistance to streptomycin, however, remained stable. Commensal human E. coli populations have clearly evolved substantially over time, presumably reflecting changes in human practices, and particularly increasing antibiotic use. |
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AbstractList | It is important to study commensal populations of Escherichia coli because they appear to be the reservoir of both extra-intestinal pathogenic E. coli and antibiotic resistant strains of E. coli. We studied 279 dominant faecal strains of E. coli from 243 adults living in the community in the Paris area in 2010. The phylogenetic group and subgroup [sequence type complex (STc)] of the isolates and the presence of 20 virulence genes were determined by PCR assays. The O-types and resistance to 18 antibiotics were assessed phenotypically. The B2 group was the most frequently recovered (34.0%), followed by the A group (28.7%), and other groups were more rare. The most prevalent B2 subgroups were II (STc73), IV (STc141), IX (STc95) and I (STc131), with 22.1, 21.1, 16.8 and 13.7%, respectively, of the B2 group strains. Virulence factors (VFs) were more common in B2 group than other strains. One or more resistances were found in 125 strains (44.8% of the collection) but only six (2.2% of the collection) were multiresistant; no extended-spectrum beta-lactamase-producing strain was isolated. The C phylogroup and clonal group A strains were the most resistant. No trade-off between virulence and resistance was evidenced. We compared these strains with collections of strains gathered under the same conditions 30 and 10 years ago. There has been a parallel and linked increase in the frequency of B2 group strains (from 9.4% in 1980, to 22.7% in 2000 and 34.0% in 2010) and of VFs. Antibiotic resistance also increased, from 22.6% of strains resistant to at least one antibiotic in 1980, to 31.8% in 2000 and 44.8% in 2010; resistance to streptomycin, however, remained stable. Commensal human E. coli populations have clearly evolved substantially over time, presumably reflecting changes in human practices, and particularly increasing antibiotic use. It is important to study commensal populations of Escherichia coli because they appear to be the reservoir of both extra-intestinal pathogenic E. coli and antibiotic resistant strains of E. coli. We studied 279 dominant faecal strains of E. coli from 243 adults living in the community in the Paris area in 2010. The phylogenetic group and sub-group [sequence type complex (STc)] of the isolates and the presence of 20 virulence genes were determined by PCR assays. The O-types and the resistance to 18 antibiotics were assessed phenotypically. The B2 group was the most frequently recovered (34.0%), followed by the A group (28.7%), and other groups were rarer. The most prevalent B2 subgroups were II (STc73), IV (STc141), IX (STc95) and I (STc131) with 22.1%, 21.1%, 16.8% and 13.7%, respectively, of the B2 group strains. Virulence factors (VFs) were more common in B2 group than other strains. One or more resistance was found in 125 strains (44.8% of the collection) but only six (2.2% of the collection) were multiresistant; no extended-spectrum beta-lactamase-producing strain was isolated. The C phylogroup and clonal group A strains were the most resistant. No trade-off between virulence and resistance was evidenced. We compared these strains to collections of strains gathered in the same conditions 30 and 10 years ago. There has been a parallel and linked increase in the frequency of B2 group strains (from 9.4% in 1980 to 22.7% in 2000 and 34.0% in 2010) and of VFs. Antibiotic resistance also increased, from 22.6% of strains resistant to at least one antibiotic in 1980 to 31.8% in 2000 and 44.8% in 2010; resistance to streptomycin, however, remained stable. Commensal human E. coli populations have clearly evolved substantially over time, presumably reflecting changes in human practices, and particularly increasing antibiotic use. It is important to study commensal populations of Escherichia coli because they appear to be the reservoir of both extra-intestinal pathogenic E. coli and antibiotic resistant strains of E. coli . We studied 279 dominant faecal strains of E. coli from 243 adults living in the community in the Paris area in 2010. The phylogenetic group and sub-group [sequence type complex (STc)]of the isolates and the presence of 20 virulence genes were determined by PCR assays. The O-types and the resistance to 18 antibiotics were assessed phenotypically. The B2 group was the most frequently recovered (34.0%), followed by the A group (28.7%), and other groups were rarer. The most prevalent B2 subgroups were II (STc73), IV (STc141), IX (STc95) and I (STc131) with 22.1%, 21.1%, 16.8% and 13.7%, respectively, of the B2 group strains. Virulence factors (VFs) were more common in B2 group than other strains. One or more resistance was found in 125 strains (44.8% of the collection) but only six (2.2% of the collection) were multiresistant; no extended-spectrum beta-lactamase-producing strain was isolated. The C phylogroup and clonal group A strains were the most resistant. No trade-off between virulence and resistance was evidenced. We compared these strains to collections of strains gathered in the same conditions 30 and 10 years ago. There has been a parallel and linked increase in the frequency of B2 group strains (from 9.4% in 1980 to 22.7% in 2000 and 34.0% in 2010)and of VFs. Antibiotic resistance also increased, from 22.6% of strains resistant to at least one antibiotic in 1980 to 31.8% in 2000 and 44.8% in 2010; resistance to streptomycin, however, remained stable. Commensal human E. coli populations have clearly evolved substantially over time, presumably reflecting changes in human practices, and particularly increasing antibiotic use. |
Author | Denamur, Erick the COLIVILLE Group Picard, Bertrand Branger, Catherine Blanco, Jorge Couffignal, Camille Mora, Azucena Jauréguy, Françoise Massot, Méril Clermont, Olivier Mentré, France Daubié, Anne-Sophie Eddi, Alain Dahbi, Ghizlane |
AuthorAffiliation | 1 IAME, Infection, Antimicrobiens, Modélisation, Evolution Université Paris Diderot - Paris 7 - Université Paris 13 - Institut National de la Santé et de la Recherche Médicale - U1137 Faculté de médecine Paris Diderot Paris 7 - site Bichat - 16 rue Henri Huchard 75890 Paris Cedex 18 4 Faculté de Médecine, Département de Médecine Générale - DMG [Paris] Université Paris Diderot - Paris 7 - Sorbonne Paris Cité - Université Paris Diderot - Faculté de Médecine - Site Bichat - (2ème étage, ascenseurs B, porte 255) - 16 rue Henri Huchard 75018 Paris 2 Hôpitaux Universitaires Paris Seine-Saint-Denis - Hôpital Avicenne (AP-HP) 3 LREC, Laboratorio de Referencia de E. coli [Lugo, Spain] Universidade de Santiago de Compostela [A Coruña, Spain] - Avda. Carballo Calero s/n., 27002 Lugo |
AuthorAffiliation_xml | – name: 2 Hôpitaux Universitaires Paris Seine-Saint-Denis - Hôpital Avicenne (AP-HP) – name: 1 IAME, Infection, Antimicrobiens, Modélisation, Evolution Université Paris Diderot - Paris 7 - Université Paris 13 - Institut National de la Santé et de la Recherche Médicale - U1137 Faculté de médecine Paris Diderot Paris 7 - site Bichat - 16 rue Henri Huchard 75890 Paris Cedex 18 – name: 3 LREC, Laboratorio de Referencia de E. coli [Lugo, Spain] Universidade de Santiago de Compostela [A Coruña, Spain] - Avda. Carballo Calero s/n., 27002 Lugo – name: 4 Faculté de Médecine, Département de Médecine Générale - DMG [Paris] Université Paris Diderot - Paris 7 - Sorbonne Paris Cité - Université Paris Diderot - Faculté de Médecine - Site Bichat - (2ème étage, ascenseurs B, porte 255) - 16 rue Henri Huchard 75018 Paris |
Author_xml | – sequence: 1 givenname: Méril surname: Massot fullname: Massot, Méril organization: INSERM, IAME, UMR1137, Paris, France, Univ Paris Diderot, IAME, UMR1137, Sorbonne Paris Cité, Paris, France – sequence: 2 givenname: Anne-Sophie surname: Daubié fullname: Daubié, Anne-Sophie organization: Univ Paris Nord, IAME, UMR1137, Sorbonne Paris Cité, Bobigny, France, APHP, Hôpitaux Universitaires Paris Seine Saint-Denis, Site Avicenne, Bobigny, France, INSERM, IAME, UMR1137, Paris, France – sequence: 3 givenname: Olivier surname: Clermont fullname: Clermont, Olivier organization: INSERM, IAME, UMR1137, Paris, France, Univ Paris Diderot, IAME, UMR1137, Sorbonne Paris Cité, Paris, France – sequence: 4 givenname: Françoise surname: Jauréguy fullname: Jauréguy, Françoise organization: INSERM, IAME, UMR1137, Paris, France, APHP, Hôpitaux Universitaires Paris Seine Saint-Denis, Site Avicenne, Bobigny, France, Univ Paris Nord, IAME, UMR1137, Sorbonne Paris Cité, Bobigny, France – sequence: 5 givenname: Camille surname: Couffignal fullname: Couffignal, Camille organization: INSERM, IAME, UMR1137, Paris, France, Univ Paris Diderot, IAME, UMR1137, Sorbonne Paris Cité, Paris, France – sequence: 6 givenname: Ghizlane surname: Dahbi fullname: Dahbi, Ghizlane organization: Laboratorio de Referencia de E. coli (LREC), Departamento de Microbioloxía e Parasitoloxía, Facultade de Veterinaria, Universidade de Santiago de Compostela (USC), Lugo, Spain – sequence: 7 givenname: Azucena surname: Mora fullname: Mora, Azucena organization: Laboratorio de Referencia de E. coli (LREC), Departamento de Microbioloxía e Parasitoloxía, Facultade de Veterinaria, Universidade de Santiago de Compostela (USC), Lugo, Spain – sequence: 8 givenname: Jorge surname: Blanco fullname: Blanco, Jorge organization: Laboratorio de Referencia de E. coli (LREC), Departamento de Microbioloxía e Parasitoloxía, Facultade de Veterinaria, Universidade de Santiago de Compostela (USC), Lugo, Spain – sequence: 9 givenname: Catherine surname: Branger fullname: Branger, Catherine organization: INSERM, IAME, UMR1137, Paris, France, Univ Paris Diderot, IAME, UMR1137, Sorbonne Paris Cité, Paris, France – sequence: 10 givenname: France surname: Mentré fullname: Mentré, France organization: INSERM, IAME, UMR1137, Paris, France, Univ Paris Diderot, IAME, UMR1137, Sorbonne Paris Cité, Paris, France – sequence: 11 givenname: Alain surname: Eddi fullname: Eddi, Alain organization: Département de Médecine Générale, Univ Paris Diderot, Sorbonne Paris Cité, Faculté de Médecine, Paris, France – sequence: 12 givenname: Bertrand surname: Picard fullname: Picard, Bertrand organization: INSERM, IAME, UMR1137, Paris, France, APHP, Hôpitaux Universitaires Paris Seine Saint-Denis, Site Avicenne, Bobigny, France, Univ Paris Nord, IAME, UMR1137, Sorbonne Paris Cité, Bobigny, France – sequence: 13 givenname: Erick surname: Denamur fullname: Denamur, Erick organization: INSERM, IAME, UMR1137, Paris, France, Univ Paris Diderot, IAME, UMR1137, Sorbonne Paris Cité, Paris, France – sequence: 14 surname: the COLIVILLE Group fullname: the COLIVILLE Group |
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References_xml | – ident: mic000242-Li1 doi: 10.1128/AEM.00707-10 – ident: mic000242-Nowrouzian1 doi: 10.1086/427996 – ident: mic000242-Partridge1 doi: 10.1111/j.1574-6976.2009.00175.x – ident: mic000242-Bailey12 doi: 10.1128/JCM.00760-10 – ident: mic000242-Lefort1 doi: 10.1128/JCM.01902-10 – ident: mic000242-Clermont1234 doi: 10.1111/1758-2229.12019 – ident: mic000242-Nicolas-Chanoine12 doi: 10.1128/CMR.00125-13 – ident: mic000242-Schubert1 doi: 10.1371/journal.ppat.1000257 – ident: mic000242-Clermont1 doi: 10.1111/j.1462-2920.2007.01520.x – ident: mic000242-Unno1 doi: 10.1128/AEM.00443-09 – ident: mic000242-Bert1 doi: 10.1128/JCM.00516-10 – ident: mic000242-Clermont12 doi: 10.1111/j.1462-2920.2011.02519.x – ident: mic000242-Duriez1 doi: 10.1099/00221287-147-6-1671 – ident: mic000242-Johnson123 doi: 10.1128/JCM.03502-13 – ident: mic000242-Kaper1 doi: 10.1038/nrmicro818 – ident: mic000242-Mahjoub-Messai1 doi: 10.1093/infdis/jir189 – ident: mic000242-Escobar-Paramo1 doi: 10.1093/molbev/msh118 – ident: mic000242-Chiew1 doi: 10.1093/jac/41.2.247 – ident: mic000242-Guinee1 doi: 10.1007/978-94-009-8328-1_18 – ident: mic000242-Nicolas-Chanoine1 doi: 10.1093/jac/dks429 – ident: mic000242-Alhashash doi: 10.3201/eid1910.130309 – ident: mic000242-Lescat1 doi: 10.1111/j.1758-2229.2012.00374.x – ident: mic000242-Walk1 doi: 10.1128/AEM.01262-09 – ident: mic000242-Moissenet1 doi: 10.1128/JCM.00529-10 – ident: mic000242-Woerther1 doi: 10.1128/AAC.00848-13 – volume: 57 start-page: 289 year: 1995 ident: mic000242-Benjamini1 article-title: Controlling the false discovery rate: a practical and powerful approach to multiple testing publication-title: J R Stat Soc B doi: 10.1111/j.2517-6161.1995.tb02031.x – ident: mic000242-Desjardins1 doi: 10.1007/BF00160315 – ident: mic000242-Johnson12 doi: 10.1128/JCM.00949-08 – ident: mic000242-Bailey1 doi: 10.1099/jmm.0.022475-0 – ident: mic000242-Diard1 doi: 10.1128/JB.00804-10 – ident: mic000242-Bengtsson1 doi: 10.1093/jac/dkr421 – ident: mic000242-Le1 doi: 10.1093/molbev/msm172 – ident: mic000242-Tapader1 doi: 10.1007/s10096-014-2161-4 – ident: mic000242-Gibreel1 doi: 10.1093/jac/dkr451 – ident: mic000242-Manges1 doi: 10.1056/NEJMoa011265 – ident: mic000242-Johnson1 doi: 10.1128/JCM.42.6.2618-2622.2004 – ident: mic000242-Russo1 doi: 10.1016/S1286-4579(03)00049-2 – ident: mic000242-Clermont123 doi: 10.1016/j.meegid.2011.02.005 – ident: mic000242-Tenaillon1 doi: 10.1038/nrmicro2298 – ident: mic000242-Berg1 doi: 10.1016/0966-842X(96)10057-3 – ident: mic000242-Clermont12345 doi: 10.1016/j.mimet.2014.03.008 – ident: mic000242-Clermont123456 doi: 10.1099/mic.0.000063 – ident: mic000242-Escobar-Paramo12 doi: 10.1128/AEM.70.9.5698-5700.2004 – ident: mic000242-Gordon1 doi: 10.1099/mic.0.27425-0 – ident: mic000242-Smati1 doi: 10.1128/AEM.01423-13 – ident: mic000242-Bidet1 doi: 10.1086/518897 – ident: mic000242-Carlet1 doi: 10.1186/2047-2994-1-39 – ident: mic000242-Messika1 doi: 10.1007/s00134-012-2699-5 |
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Snippet | It is important to study commensal populations of Escherichia coli because they appear to be the reservoir of both extra-intestinal pathogenic E. coli and... It is important to study commensal populations of Escherichia coli because they appear to be the reservoir of both extra-intestinal pathogenic E. coli and... |
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SubjectTerms | Drug Resistance, Bacterial Escherichia coli Escherichia coli - classification Escherichia coli - drug effects Escherichia coli - genetics Escherichia coli - isolation & purification Feces - microbiology Genotype Humans Life Sciences Microbiology and Parasitology Molecular Typing O Antigens - analysis Paris Phylogeny Polymerase Chain Reaction Sequence Analysis, DNA Serogroup Time Factors Virulence Factors - analysis Virulence Factors - genetics |
Title | Phylogenetic, virulence and antibiotic resistance characteristics of commensal strain populations of Escherichia coli from community subjects in the Paris area in 2010 and evolution over 30 years |
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