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Gene Fitness Landscapes of Vibrio cholerae at Important Stages of Its Life Cycle
Vibrio cholerae has evolved to adeptly transition between the human small intestine and aquatic environments, leading to water-borne spread and transmission of the lethal diarrheal disease cholera. Using a host model that mimics the pathology of human cholera, we applied high density transposon muta...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3873450/ https://www.ncbi.nlm.nih.gov/pubmed/24385900 http://dx.doi.org/10.1371/journal.ppat.1003800 |
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author | Kamp, Heather D. Patimalla-Dipali, Bharathi Lazinski, David W. Wallace-Gadsden, Faith Camilli, Andrew |
author_facet | Kamp, Heather D. Patimalla-Dipali, Bharathi Lazinski, David W. Wallace-Gadsden, Faith Camilli, Andrew |
author_sort | Kamp, Heather D. |
collection | PubMed |
description | Vibrio cholerae has evolved to adeptly transition between the human small intestine and aquatic environments, leading to water-borne spread and transmission of the lethal diarrheal disease cholera. Using a host model that mimics the pathology of human cholera, we applied high density transposon mutagenesis combined with massively parallel sequencing (Tn-seq) to determine the fitness contribution of >90% of all non-essential genes of V. cholerae both during host infection and dissemination. Targeted mutagenesis and validation of 35 genes confirmed our results for the selective conditions with a total false positive rate of 4%. We identified 165 genes never before implicated for roles in dissemination that reside within pathways controlling many metabolic, catabolic and protective processes, from which a central role for glycogen metabolism was revealed. We additionally identified 76 new pathogenicity factors and 414 putatively essential genes for V. cholerae growth. Our results provide a comprehensive framework for understanding the biology of V. cholerae as it colonizes the small intestine, elicits profuse secretory diarrhea, and disseminates into the aquatic environment. |
format | Online Article Text |
id | pubmed-3873450 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-38734502014-01-02 Gene Fitness Landscapes of Vibrio cholerae at Important Stages of Its Life Cycle Kamp, Heather D. Patimalla-Dipali, Bharathi Lazinski, David W. Wallace-Gadsden, Faith Camilli, Andrew PLoS Pathog Research Article Vibrio cholerae has evolved to adeptly transition between the human small intestine and aquatic environments, leading to water-borne spread and transmission of the lethal diarrheal disease cholera. Using a host model that mimics the pathology of human cholera, we applied high density transposon mutagenesis combined with massively parallel sequencing (Tn-seq) to determine the fitness contribution of >90% of all non-essential genes of V. cholerae both during host infection and dissemination. Targeted mutagenesis and validation of 35 genes confirmed our results for the selective conditions with a total false positive rate of 4%. We identified 165 genes never before implicated for roles in dissemination that reside within pathways controlling many metabolic, catabolic and protective processes, from which a central role for glycogen metabolism was revealed. We additionally identified 76 new pathogenicity factors and 414 putatively essential genes for V. cholerae growth. Our results provide a comprehensive framework for understanding the biology of V. cholerae as it colonizes the small intestine, elicits profuse secretory diarrhea, and disseminates into the aquatic environment. Public Library of Science 2013-12-26 /pmc/articles/PMC3873450/ /pubmed/24385900 http://dx.doi.org/10.1371/journal.ppat.1003800 Text en © 2013 Kamp 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 Kamp, Heather D. Patimalla-Dipali, Bharathi Lazinski, David W. Wallace-Gadsden, Faith Camilli, Andrew Gene Fitness Landscapes of Vibrio cholerae at Important Stages of Its Life Cycle |
title | Gene Fitness Landscapes of Vibrio cholerae at Important Stages of Its Life Cycle |
title_full | Gene Fitness Landscapes of Vibrio cholerae at Important Stages of Its Life Cycle |
title_fullStr | Gene Fitness Landscapes of Vibrio cholerae at Important Stages of Its Life Cycle |
title_full_unstemmed | Gene Fitness Landscapes of Vibrio cholerae at Important Stages of Its Life Cycle |
title_short | Gene Fitness Landscapes of Vibrio cholerae at Important Stages of Its Life Cycle |
title_sort | gene fitness landscapes of vibrio cholerae at important stages of its life cycle |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3873450/ https://www.ncbi.nlm.nih.gov/pubmed/24385900 http://dx.doi.org/10.1371/journal.ppat.1003800 |
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