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Identification of genes required for the survival of B. fragilis using massive parallel sequencing of a saturated transposon mutant library

BACKGROUND: Bacteroides fragilis is a Gram-negative anaerobe that is normally a human gut commensal; it comprises a small percentage of the gut Bacteroides but is the most frequently isolated Bacteroides from human infections. Identification of the essential genes necessary for the survival of B. fr...

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Autores principales: Veeranagouda, Yaligara, Husain, Fasahath, Tenorio, Elizabeth L, Wexler, Hannah M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4072883/
https://www.ncbi.nlm.nih.gov/pubmed/24899126
http://dx.doi.org/10.1186/1471-2164-15-429
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author Veeranagouda, Yaligara
Husain, Fasahath
Tenorio, Elizabeth L
Wexler, Hannah M
author_facet Veeranagouda, Yaligara
Husain, Fasahath
Tenorio, Elizabeth L
Wexler, Hannah M
author_sort Veeranagouda, Yaligara
collection PubMed
description BACKGROUND: Bacteroides fragilis is a Gram-negative anaerobe that is normally a human gut commensal; it comprises a small percentage of the gut Bacteroides but is the most frequently isolated Bacteroides from human infections. Identification of the essential genes necessary for the survival of B. fragilis provides novel information which can be exploited for the treatment of bacterial infections. RESULTS: Massive parallel sequencing of saturated transposon mutant libraries (two mutant pools of approximately 50,000 mutants each) was used to determine the essential genes for the growth of B. fragilis 638R on nutrient rich medium. Among the 4326 protein coding genes, 550 genes (12.7%) were found to be essential for the survival of B. fragilis 638R. Of the 550 essential genes, only 367 genes were assigned to a Cluster of Orthologous Genes, and about 290 genes had Kyoto Encyclopedia of Genes and Genomes orthologous members. Interestingly, genes with hypothetical functions accounted for 41.3% of essential genes (227 genes), indicating that the functions of a significant percentage of the genes used by B. fragilis 638R are still unknown. Global transcriptome analysis using RNA-Seq indicated that most of the essential genes (92%) are, in fact, transcribed in B. fragilis 638R including most of those coding for hypothetical proteins. Three hundred fifty of the 550 essential genes of B. fragilis 638R are present in Database of Essential Genes. 10.02 and 31% of those are genes included as essential genes for nine species (including Gram-positive pathogenic bacteria). CONCLUSIONS: The essential gene data described in this investigation provides a valuable resource to study gene function and pathways involved in B. fragilis survival. Thorough examination of the B. fragilis-specific essential genes and genes that are shared between divergent organisms opens new research avenues that will lead to enhanced understanding of survival strategies used by bacteria in different microniches and under different stress situations. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi: 10.1186/1471-2164-15-429) contains supplementary material, which is available to authorized users.
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spelling pubmed-40728832014-07-01 Identification of genes required for the survival of B. fragilis using massive parallel sequencing of a saturated transposon mutant library Veeranagouda, Yaligara Husain, Fasahath Tenorio, Elizabeth L Wexler, Hannah M BMC Genomics Research Article BACKGROUND: Bacteroides fragilis is a Gram-negative anaerobe that is normally a human gut commensal; it comprises a small percentage of the gut Bacteroides but is the most frequently isolated Bacteroides from human infections. Identification of the essential genes necessary for the survival of B. fragilis provides novel information which can be exploited for the treatment of bacterial infections. RESULTS: Massive parallel sequencing of saturated transposon mutant libraries (two mutant pools of approximately 50,000 mutants each) was used to determine the essential genes for the growth of B. fragilis 638R on nutrient rich medium. Among the 4326 protein coding genes, 550 genes (12.7%) were found to be essential for the survival of B. fragilis 638R. Of the 550 essential genes, only 367 genes were assigned to a Cluster of Orthologous Genes, and about 290 genes had Kyoto Encyclopedia of Genes and Genomes orthologous members. Interestingly, genes with hypothetical functions accounted for 41.3% of essential genes (227 genes), indicating that the functions of a significant percentage of the genes used by B. fragilis 638R are still unknown. Global transcriptome analysis using RNA-Seq indicated that most of the essential genes (92%) are, in fact, transcribed in B. fragilis 638R including most of those coding for hypothetical proteins. Three hundred fifty of the 550 essential genes of B. fragilis 638R are present in Database of Essential Genes. 10.02 and 31% of those are genes included as essential genes for nine species (including Gram-positive pathogenic bacteria). CONCLUSIONS: The essential gene data described in this investigation provides a valuable resource to study gene function and pathways involved in B. fragilis survival. Thorough examination of the B. fragilis-specific essential genes and genes that are shared between divergent organisms opens new research avenues that will lead to enhanced understanding of survival strategies used by bacteria in different microniches and under different stress situations. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi: 10.1186/1471-2164-15-429) contains supplementary material, which is available to authorized users. BioMed Central 2014-06-04 /pmc/articles/PMC4072883/ /pubmed/24899126 http://dx.doi.org/10.1186/1471-2164-15-429 Text en © Veeranagouda et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Veeranagouda, Yaligara
Husain, Fasahath
Tenorio, Elizabeth L
Wexler, Hannah M
Identification of genes required for the survival of B. fragilis using massive parallel sequencing of a saturated transposon mutant library
title Identification of genes required for the survival of B. fragilis using massive parallel sequencing of a saturated transposon mutant library
title_full Identification of genes required for the survival of B. fragilis using massive parallel sequencing of a saturated transposon mutant library
title_fullStr Identification of genes required for the survival of B. fragilis using massive parallel sequencing of a saturated transposon mutant library
title_full_unstemmed Identification of genes required for the survival of B. fragilis using massive parallel sequencing of a saturated transposon mutant library
title_short Identification of genes required for the survival of B. fragilis using massive parallel sequencing of a saturated transposon mutant library
title_sort identification of genes required for the survival of b. fragilis using massive parallel sequencing of a saturated transposon mutant library
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4072883/
https://www.ncbi.nlm.nih.gov/pubmed/24899126
http://dx.doi.org/10.1186/1471-2164-15-429
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