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A fine scale phenotype–genotype virulence map of a bacterial pathogen
A large fraction of the genes from sequenced organisms are of unknown function. This limits biological insight, and for pathogenic microorganisms hampers the development of new approaches to battle infections. There is thus a great need for novel strategies that link genotypes to phenotypes for micr...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3514683/ https://www.ncbi.nlm.nih.gov/pubmed/22826510 http://dx.doi.org/10.1101/gr.137430.112 |
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author | van Opijnen, Tim Camilli, Andrew |
author_facet | van Opijnen, Tim Camilli, Andrew |
author_sort | van Opijnen, Tim |
collection | PubMed |
description | A large fraction of the genes from sequenced organisms are of unknown function. This limits biological insight, and for pathogenic microorganisms hampers the development of new approaches to battle infections. There is thus a great need for novel strategies that link genotypes to phenotypes for microorganisms. We describe a high-throughput strategy based on the method Tn-seq that can be applied to any genetically manipulatable microorganism. By screening 17 in vitro and two in vivo (carriage and infection) conditions for the pathogen Streptococcus pneumoniae, we create a resource consisting of >1800 interactions that is rich in new genotype–phenotype relationships. We describe genes that are involved in differential carbon source utilization in the host, as well as genes that are involved both in virulence and in resistance against specific in vitro stresses, thereby revealing selection pressures that the pathogen experiences in vivo. We reveal the secondary response to an antibiotic, including a dual role efflux pump also involved in resistance to pH stress. Through genetic-interaction mapping and gene-expression analysis we define the mechanism of attenuation and the regulatory relationship between a two-component system and a core biosynthetic pathway specific to microorganisms. Thus, we have generated a resource that provides detailed insight into the biology and virulence of S. pneumoniae and provided a road map for similar discovery in other microorganisms. |
format | Online Article Text |
id | pubmed-3514683 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-35146832013-06-01 A fine scale phenotype–genotype virulence map of a bacterial pathogen van Opijnen, Tim Camilli, Andrew Genome Res Resource A large fraction of the genes from sequenced organisms are of unknown function. This limits biological insight, and for pathogenic microorganisms hampers the development of new approaches to battle infections. There is thus a great need for novel strategies that link genotypes to phenotypes for microorganisms. We describe a high-throughput strategy based on the method Tn-seq that can be applied to any genetically manipulatable microorganism. By screening 17 in vitro and two in vivo (carriage and infection) conditions for the pathogen Streptococcus pneumoniae, we create a resource consisting of >1800 interactions that is rich in new genotype–phenotype relationships. We describe genes that are involved in differential carbon source utilization in the host, as well as genes that are involved both in virulence and in resistance against specific in vitro stresses, thereby revealing selection pressures that the pathogen experiences in vivo. We reveal the secondary response to an antibiotic, including a dual role efflux pump also involved in resistance to pH stress. Through genetic-interaction mapping and gene-expression analysis we define the mechanism of attenuation and the regulatory relationship between a two-component system and a core biosynthetic pathway specific to microorganisms. Thus, we have generated a resource that provides detailed insight into the biology and virulence of S. pneumoniae and provided a road map for similar discovery in other microorganisms. Cold Spring Harbor Laboratory Press 2012-12 /pmc/articles/PMC3514683/ /pubmed/22826510 http://dx.doi.org/10.1101/gr.137430.112 Text en © 2012, Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genome.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 3.0 Unported License), as described at http://creativecommons.org/licenses/by-nc/3.0/. |
spellingShingle | Resource van Opijnen, Tim Camilli, Andrew A fine scale phenotype–genotype virulence map of a bacterial pathogen |
title | A fine scale phenotype–genotype virulence map of a bacterial pathogen |
title_full | A fine scale phenotype–genotype virulence map of a bacterial pathogen |
title_fullStr | A fine scale phenotype–genotype virulence map of a bacterial pathogen |
title_full_unstemmed | A fine scale phenotype–genotype virulence map of a bacterial pathogen |
title_short | A fine scale phenotype–genotype virulence map of a bacterial pathogen |
title_sort | fine scale phenotype–genotype virulence map of a bacterial pathogen |
topic | Resource |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3514683/ https://www.ncbi.nlm.nih.gov/pubmed/22826510 http://dx.doi.org/10.1101/gr.137430.112 |
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