Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Kamp, Heather D., Patimalla-Dipali, Bharathi, Lazinski, David W., Wallace-Gadsden, Faith, Camilli, Andrew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
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
_version_ 1782297117593698304
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
work_keys_str_mv AT kampheatherd genefitnesslandscapesofvibriocholeraeatimportantstagesofitslifecycle
AT patimalladipalibharathi genefitnesslandscapesofvibriocholeraeatimportantstagesofitslifecycle
AT lazinskidavidw genefitnesslandscapesofvibriocholeraeatimportantstagesofitslifecycle
AT wallacegadsdenfaith genefitnesslandscapesofvibriocholeraeatimportantstagesofitslifecycle
AT camilliandrew genefitnesslandscapesofvibriocholeraeatimportantstagesofitslifecycle