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Examination of the Enterotoxigenic Escherichia coli Population Structure during Human Infection
Enterotoxigenic E. coli (ETEC) can cause severe diarrhea and death in children in developing countries; however, bacterial diversity in natural infection is uncharacterized. In this study, we explored the natural population variation of ETEC from individuals with cholera-like diarrhea. Genomic seque...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Microbiology
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4462620/ https://www.ncbi.nlm.nih.gov/pubmed/26060273 http://dx.doi.org/10.1128/mBio.00501-15 |
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author | Sahl, Jason W. Sistrunk, Jeticia R. Fraser, Claire M. Hine, Erin Baby, Nabilah Begum, Yasmin Luo, Qingwei Sheikh, Alaullah Qadri, Firdausi Fleckenstein, James M. Rasko, David A. |
author_facet | Sahl, Jason W. Sistrunk, Jeticia R. Fraser, Claire M. Hine, Erin Baby, Nabilah Begum, Yasmin Luo, Qingwei Sheikh, Alaullah Qadri, Firdausi Fleckenstein, James M. Rasko, David A. |
author_sort | Sahl, Jason W. |
collection | PubMed |
description | Enterotoxigenic E. coli (ETEC) can cause severe diarrhea and death in children in developing countries; however, bacterial diversity in natural infection is uncharacterized. In this study, we explored the natural population variation of ETEC from individuals with cholera-like diarrhea. Genomic sequencing and comparative analysis of multiple ETEC isolates from twelve cases of severe diarrhea demonstrated clonal populations in the majority of subjects (10/12). In contrast, a minority of individuals (2/12) yielded phylogenomically divergent ETEC isolates. Detailed examination revealed that isolates also differed in virulence factor content. These genomic data suggest that severe, cholera-like ETEC infections are largely caused by a clonal population of organisms within individual patients. Additionally, the isolation of similar clones from geographically and temporally dispersed cases with similar clinical presentations suggests that some isolates are particularly suited for virulence. The identification of multiple genomically diverse isolates with variable virulence factor profiles from a single subject highlights the dynamic nature of ETEC, as well as a potential weakness in the examination of cultures obtained from a single colony in clinical settings. These findings have implications for vaccine design and provide a framework for the study of population variation in other human pathogens. |
format | Online Article Text |
id | pubmed-4462620 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | American Society of Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-44626202015-06-19 Examination of the Enterotoxigenic Escherichia coli Population Structure during Human Infection Sahl, Jason W. Sistrunk, Jeticia R. Fraser, Claire M. Hine, Erin Baby, Nabilah Begum, Yasmin Luo, Qingwei Sheikh, Alaullah Qadri, Firdausi Fleckenstein, James M. Rasko, David A. mBio Observation Enterotoxigenic E. coli (ETEC) can cause severe diarrhea and death in children in developing countries; however, bacterial diversity in natural infection is uncharacterized. In this study, we explored the natural population variation of ETEC from individuals with cholera-like diarrhea. Genomic sequencing and comparative analysis of multiple ETEC isolates from twelve cases of severe diarrhea demonstrated clonal populations in the majority of subjects (10/12). In contrast, a minority of individuals (2/12) yielded phylogenomically divergent ETEC isolates. Detailed examination revealed that isolates also differed in virulence factor content. These genomic data suggest that severe, cholera-like ETEC infections are largely caused by a clonal population of organisms within individual patients. Additionally, the isolation of similar clones from geographically and temporally dispersed cases with similar clinical presentations suggests that some isolates are particularly suited for virulence. The identification of multiple genomically diverse isolates with variable virulence factor profiles from a single subject highlights the dynamic nature of ETEC, as well as a potential weakness in the examination of cultures obtained from a single colony in clinical settings. These findings have implications for vaccine design and provide a framework for the study of population variation in other human pathogens. American Society of Microbiology 2015-06-09 /pmc/articles/PMC4462620/ /pubmed/26060273 http://dx.doi.org/10.1128/mBio.00501-15 Text en Copyright © 2015 Sahl et al. http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-ShareAlike 3.0 Unported license (http://creativecommons.org/licenses/by-nc-sa/3.0/) , which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Observation Sahl, Jason W. Sistrunk, Jeticia R. Fraser, Claire M. Hine, Erin Baby, Nabilah Begum, Yasmin Luo, Qingwei Sheikh, Alaullah Qadri, Firdausi Fleckenstein, James M. Rasko, David A. Examination of the Enterotoxigenic Escherichia coli Population Structure during Human Infection |
title | Examination of the Enterotoxigenic Escherichia coli Population Structure during Human Infection |
title_full | Examination of the Enterotoxigenic Escherichia coli Population Structure during Human Infection |
title_fullStr | Examination of the Enterotoxigenic Escherichia coli Population Structure during Human Infection |
title_full_unstemmed | Examination of the Enterotoxigenic Escherichia coli Population Structure during Human Infection |
title_short | Examination of the Enterotoxigenic Escherichia coli Population Structure during Human Infection |
title_sort | examination of the enterotoxigenic escherichia coli population structure during human infection |
topic | Observation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4462620/ https://www.ncbi.nlm.nih.gov/pubmed/26060273 http://dx.doi.org/10.1128/mBio.00501-15 |
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