Molecular and evolutionary bases of within-patient genotypic and phenotypic diversity in Escherichia coli extraintestinal infections.
Although polymicrobial infections, caused by combinations of viruses, bacteria, fungi and parasites, are being recognised with increasing frequency, little is known about the occurrence of within-species diversity in bacterial infections and the molecular and evolutionary bases of this diversity. We...
Guardado en:
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Public Library of Science (PLoS)
2010
|
Materias: | |
Acceso en línea: | https://doaj.org/article/e7451ec319ce496eb724fc67d8419d94 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
id |
oai:doaj.org-article:e7451ec319ce496eb724fc67d8419d94 |
---|---|
record_format |
dspace |
spelling |
oai:doaj.org-article:e7451ec319ce496eb724fc67d8419d942021-11-18T06:03:53ZMolecular and evolutionary bases of within-patient genotypic and phenotypic diversity in Escherichia coli extraintestinal infections.1553-73661553-737410.1371/journal.ppat.1001125https://doaj.org/article/e7451ec319ce496eb724fc67d8419d942010-09-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20941353/pdf/?tool=EBIhttps://doaj.org/toc/1553-7366https://doaj.org/toc/1553-7374Although polymicrobial infections, caused by combinations of viruses, bacteria, fungi and parasites, are being recognised with increasing frequency, little is known about the occurrence of within-species diversity in bacterial infections and the molecular and evolutionary bases of this diversity. We used multiple approaches to study the genomic and phenotypic diversity among 226 Escherichia coli isolates from deep and closed visceral infections occurring in 19 patients. We observed genomic variability among isolates from the same site within 11 patients. This diversity was of two types, as patients were infected either by several distinct E. coli clones (4 patients) or by members of a single clone that exhibit micro-heterogeneity (11 patients); both types of diversity were present in 4 patients. A surprisingly wide continuum of antibiotic resistance, outer membrane permeability, growth rate, stress resistance, red dry and rough morphotype characteristics and virulence properties were present within the isolates of single clones in 8 of the 11 patients showing genomic micro-heterogeneity. Many of the observed phenotypic differences within clones affected the trade-off between self-preservation and nutritional competence (SPANC). We showed in 3 patients that this phenotypic variability was associated with distinct levels of RpoS in co-existing isolates. Genome mutational analysis and global proteomic comparisons in isolates from a patient revealed a star-like relationship of changes amongst clonally diverging isolates. A mathematical model demonstrated that multiple genotypes with distinct RpoS levels can co-exist as a result of the SPANC trade-off. In the cases involving infection by a single clone, we present several lines of evidence to suggest diversification during the infectious process rather than an infection by multiple isolates exhibiting a micro-heterogeneity. Our results suggest that bacteria are subject to trade-offs during an infectious process and that the observed diversity resembled results obtained in experimental evolution studies. Whatever the mechanisms leading to diversity, our results have strong medical implications in terms of the need for more extensive isolate testing before deciding on antibiotic therapies.Maxime LevertOana ZamfirOlivier ClermontOdile BouvetSylvain LespinatsMarie Claire HipeauxCatherine BrangerBertrand PicardClaude Saint-RufFrançoise NorelThierry BalliauMichel ZivyHervé Le NagardStéphane CruveillerBéatrice Chane-Woon-MingSusanna NilssonIvana GudeljKatherine PhanThomas FerenciOlivier TenaillonErick DenamurPublic Library of Science (PLoS)articleImmunologic diseases. AllergyRC581-607Biology (General)QH301-705.5ENPLoS Pathogens, Vol 6, Iss 9, p e1001125 (2010) |
institution |
DOAJ |
collection |
DOAJ |
language |
EN |
topic |
Immunologic diseases. Allergy RC581-607 Biology (General) QH301-705.5 |
spellingShingle |
Immunologic diseases. Allergy RC581-607 Biology (General) QH301-705.5 Maxime Levert Oana Zamfir Olivier Clermont Odile Bouvet Sylvain Lespinats Marie Claire Hipeaux Catherine Branger Bertrand Picard Claude Saint-Ruf Françoise Norel Thierry Balliau Michel Zivy Hervé Le Nagard Stéphane Cruveiller Béatrice Chane-Woon-Ming Susanna Nilsson Ivana Gudelj Katherine Phan Thomas Ferenci Olivier Tenaillon Erick Denamur Molecular and evolutionary bases of within-patient genotypic and phenotypic diversity in Escherichia coli extraintestinal infections. |
description |
Although polymicrobial infections, caused by combinations of viruses, bacteria, fungi and parasites, are being recognised with increasing frequency, little is known about the occurrence of within-species diversity in bacterial infections and the molecular and evolutionary bases of this diversity. We used multiple approaches to study the genomic and phenotypic diversity among 226 Escherichia coli isolates from deep and closed visceral infections occurring in 19 patients. We observed genomic variability among isolates from the same site within 11 patients. This diversity was of two types, as patients were infected either by several distinct E. coli clones (4 patients) or by members of a single clone that exhibit micro-heterogeneity (11 patients); both types of diversity were present in 4 patients. A surprisingly wide continuum of antibiotic resistance, outer membrane permeability, growth rate, stress resistance, red dry and rough morphotype characteristics and virulence properties were present within the isolates of single clones in 8 of the 11 patients showing genomic micro-heterogeneity. Many of the observed phenotypic differences within clones affected the trade-off between self-preservation and nutritional competence (SPANC). We showed in 3 patients that this phenotypic variability was associated with distinct levels of RpoS in co-existing isolates. Genome mutational analysis and global proteomic comparisons in isolates from a patient revealed a star-like relationship of changes amongst clonally diverging isolates. A mathematical model demonstrated that multiple genotypes with distinct RpoS levels can co-exist as a result of the SPANC trade-off. In the cases involving infection by a single clone, we present several lines of evidence to suggest diversification during the infectious process rather than an infection by multiple isolates exhibiting a micro-heterogeneity. Our results suggest that bacteria are subject to trade-offs during an infectious process and that the observed diversity resembled results obtained in experimental evolution studies. Whatever the mechanisms leading to diversity, our results have strong medical implications in terms of the need for more extensive isolate testing before deciding on antibiotic therapies. |
format |
article |
author |
Maxime Levert Oana Zamfir Olivier Clermont Odile Bouvet Sylvain Lespinats Marie Claire Hipeaux Catherine Branger Bertrand Picard Claude Saint-Ruf Françoise Norel Thierry Balliau Michel Zivy Hervé Le Nagard Stéphane Cruveiller Béatrice Chane-Woon-Ming Susanna Nilsson Ivana Gudelj Katherine Phan Thomas Ferenci Olivier Tenaillon Erick Denamur |
author_facet |
Maxime Levert Oana Zamfir Olivier Clermont Odile Bouvet Sylvain Lespinats Marie Claire Hipeaux Catherine Branger Bertrand Picard Claude Saint-Ruf Françoise Norel Thierry Balliau Michel Zivy Hervé Le Nagard Stéphane Cruveiller Béatrice Chane-Woon-Ming Susanna Nilsson Ivana Gudelj Katherine Phan Thomas Ferenci Olivier Tenaillon Erick Denamur |
author_sort |
Maxime Levert |
title |
Molecular and evolutionary bases of within-patient genotypic and phenotypic diversity in Escherichia coli extraintestinal infections. |
title_short |
Molecular and evolutionary bases of within-patient genotypic and phenotypic diversity in Escherichia coli extraintestinal infections. |
title_full |
Molecular and evolutionary bases of within-patient genotypic and phenotypic diversity in Escherichia coli extraintestinal infections. |
title_fullStr |
Molecular and evolutionary bases of within-patient genotypic and phenotypic diversity in Escherichia coli extraintestinal infections. |
title_full_unstemmed |
Molecular and evolutionary bases of within-patient genotypic and phenotypic diversity in Escherichia coli extraintestinal infections. |
title_sort |
molecular and evolutionary bases of within-patient genotypic and phenotypic diversity in escherichia coli extraintestinal infections. |
publisher |
Public Library of Science (PLoS) |
publishDate |
2010 |
url |
https://doaj.org/article/e7451ec319ce496eb724fc67d8419d94 |
work_keys_str_mv |
AT maximelevert molecularandevolutionarybasesofwithinpatientgenotypicandphenotypicdiversityinescherichiacoliextraintestinalinfections AT oanazamfir molecularandevolutionarybasesofwithinpatientgenotypicandphenotypicdiversityinescherichiacoliextraintestinalinfections AT olivierclermont molecularandevolutionarybasesofwithinpatientgenotypicandphenotypicdiversityinescherichiacoliextraintestinalinfections AT odilebouvet molecularandevolutionarybasesofwithinpatientgenotypicandphenotypicdiversityinescherichiacoliextraintestinalinfections AT sylvainlespinats molecularandevolutionarybasesofwithinpatientgenotypicandphenotypicdiversityinescherichiacoliextraintestinalinfections AT marieclairehipeaux molecularandevolutionarybasesofwithinpatientgenotypicandphenotypicdiversityinescherichiacoliextraintestinalinfections AT catherinebranger molecularandevolutionarybasesofwithinpatientgenotypicandphenotypicdiversityinescherichiacoliextraintestinalinfections AT bertrandpicard molecularandevolutionarybasesofwithinpatientgenotypicandphenotypicdiversityinescherichiacoliextraintestinalinfections AT claudesaintruf molecularandevolutionarybasesofwithinpatientgenotypicandphenotypicdiversityinescherichiacoliextraintestinalinfections AT francoisenorel molecularandevolutionarybasesofwithinpatientgenotypicandphenotypicdiversityinescherichiacoliextraintestinalinfections AT thierryballiau molecularandevolutionarybasesofwithinpatientgenotypicandphenotypicdiversityinescherichiacoliextraintestinalinfections AT michelzivy molecularandevolutionarybasesofwithinpatientgenotypicandphenotypicdiversityinescherichiacoliextraintestinalinfections AT hervelenagard molecularandevolutionarybasesofwithinpatientgenotypicandphenotypicdiversityinescherichiacoliextraintestinalinfections AT stephanecruveiller molecularandevolutionarybasesofwithinpatientgenotypicandphenotypicdiversityinescherichiacoliextraintestinalinfections AT beatricechanewoonming molecularandevolutionarybasesofwithinpatientgenotypicandphenotypicdiversityinescherichiacoliextraintestinalinfections AT susannanilsson molecularandevolutionarybasesofwithinpatientgenotypicandphenotypicdiversityinescherichiacoliextraintestinalinfections AT ivanagudelj molecularandevolutionarybasesofwithinpatientgenotypicandphenotypicdiversityinescherichiacoliextraintestinalinfections AT katherinephan molecularandevolutionarybasesofwithinpatientgenotypicandphenotypicdiversityinescherichiacoliextraintestinalinfections AT thomasferenci molecularandevolutionarybasesofwithinpatientgenotypicandphenotypicdiversityinescherichiacoliextraintestinalinfections AT oliviertenaillon molecularandevolutionarybasesofwithinpatientgenotypicandphenotypicdiversityinescherichiacoliextraintestinalinfections AT erickdenamur molecularandevolutionarybasesofwithinpatientgenotypicandphenotypicdiversityinescherichiacoliextraintestinalinfections |
_version_ |
1718424638966464512 |