Cargando…

ARTIST: High-Resolution Genome-Wide Assessment of Fitness Using Transposon-Insertion Sequencing

Transposon-insertion sequencing (TIS) is a powerful approach for deciphering genetic requirements for bacterial growth in different conditions, as it enables simultaneous genome-wide analysis of the fitness of thousands of mutants. However, current methods for comparative analysis of TIS data do not...

Descripción completa

Detalles Bibliográficos
Autores principales: Pritchard, Justin R., Chao, Michael C., Abel, Sören, Davis, Brigid M., Baranowski, Catherine, Zhang, Yanjia J., Rubin, Eric J., Waldor, Matthew K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4222735/
https://www.ncbi.nlm.nih.gov/pubmed/25375795
http://dx.doi.org/10.1371/journal.pgen.1004782
_version_ 1782343092926414848
author Pritchard, Justin R.
Chao, Michael C.
Abel, Sören
Davis, Brigid M.
Baranowski, Catherine
Zhang, Yanjia J.
Rubin, Eric J.
Waldor, Matthew K.
author_facet Pritchard, Justin R.
Chao, Michael C.
Abel, Sören
Davis, Brigid M.
Baranowski, Catherine
Zhang, Yanjia J.
Rubin, Eric J.
Waldor, Matthew K.
author_sort Pritchard, Justin R.
collection PubMed
description Transposon-insertion sequencing (TIS) is a powerful approach for deciphering genetic requirements for bacterial growth in different conditions, as it enables simultaneous genome-wide analysis of the fitness of thousands of mutants. However, current methods for comparative analysis of TIS data do not adjust for stochastic experimental variation between datasets and are limited to interrogation of annotated genomic elements. Here, we present ARTIST, an accessible TIS analysis pipeline for identifying essential regions that are required for growth under optimal conditions as well as conditionally essential loci that participate in survival only under specific conditions. ARTIST uses simulation-based normalization to model and compensate for experimental noise, and thereby enhances the statistical power in conditional TIS analyses. ARTIST also employs a novel adaptation of the hidden Markov model to generate statistically robust, high-resolution, annotation-independent maps of fitness-linked loci across the entire genome. Using ARTIST, we sensitively and comprehensively define Mycobacterium tuberculosis and Vibrio cholerae loci required for host infection while limiting inclusion of false positive loci. ARTIST is applicable to a broad range of organisms and will facilitate TIS-based dissection of pathways required for microbial growth and survival under a multitude of conditions.
format Online
Article
Text
id pubmed-4222735
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-42227352014-11-13 ARTIST: High-Resolution Genome-Wide Assessment of Fitness Using Transposon-Insertion Sequencing Pritchard, Justin R. Chao, Michael C. Abel, Sören Davis, Brigid M. Baranowski, Catherine Zhang, Yanjia J. Rubin, Eric J. Waldor, Matthew K. PLoS Genet Research Article Transposon-insertion sequencing (TIS) is a powerful approach for deciphering genetic requirements for bacterial growth in different conditions, as it enables simultaneous genome-wide analysis of the fitness of thousands of mutants. However, current methods for comparative analysis of TIS data do not adjust for stochastic experimental variation between datasets and are limited to interrogation of annotated genomic elements. Here, we present ARTIST, an accessible TIS analysis pipeline for identifying essential regions that are required for growth under optimal conditions as well as conditionally essential loci that participate in survival only under specific conditions. ARTIST uses simulation-based normalization to model and compensate for experimental noise, and thereby enhances the statistical power in conditional TIS analyses. ARTIST also employs a novel adaptation of the hidden Markov model to generate statistically robust, high-resolution, annotation-independent maps of fitness-linked loci across the entire genome. Using ARTIST, we sensitively and comprehensively define Mycobacterium tuberculosis and Vibrio cholerae loci required for host infection while limiting inclusion of false positive loci. ARTIST is applicable to a broad range of organisms and will facilitate TIS-based dissection of pathways required for microbial growth and survival under a multitude of conditions. Public Library of Science 2014-11-06 /pmc/articles/PMC4222735/ /pubmed/25375795 http://dx.doi.org/10.1371/journal.pgen.1004782 Text en © 2014 Pritchard 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
Pritchard, Justin R.
Chao, Michael C.
Abel, Sören
Davis, Brigid M.
Baranowski, Catherine
Zhang, Yanjia J.
Rubin, Eric J.
Waldor, Matthew K.
ARTIST: High-Resolution Genome-Wide Assessment of Fitness Using Transposon-Insertion Sequencing
title ARTIST: High-Resolution Genome-Wide Assessment of Fitness Using Transposon-Insertion Sequencing
title_full ARTIST: High-Resolution Genome-Wide Assessment of Fitness Using Transposon-Insertion Sequencing
title_fullStr ARTIST: High-Resolution Genome-Wide Assessment of Fitness Using Transposon-Insertion Sequencing
title_full_unstemmed ARTIST: High-Resolution Genome-Wide Assessment of Fitness Using Transposon-Insertion Sequencing
title_short ARTIST: High-Resolution Genome-Wide Assessment of Fitness Using Transposon-Insertion Sequencing
title_sort artist: high-resolution genome-wide assessment of fitness using transposon-insertion sequencing
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4222735/
https://www.ncbi.nlm.nih.gov/pubmed/25375795
http://dx.doi.org/10.1371/journal.pgen.1004782
work_keys_str_mv AT pritchardjustinr artisthighresolutiongenomewideassessmentoffitnessusingtransposoninsertionsequencing
AT chaomichaelc artisthighresolutiongenomewideassessmentoffitnessusingtransposoninsertionsequencing
AT abelsoren artisthighresolutiongenomewideassessmentoffitnessusingtransposoninsertionsequencing
AT davisbrigidm artisthighresolutiongenomewideassessmentoffitnessusingtransposoninsertionsequencing
AT baranowskicatherine artisthighresolutiongenomewideassessmentoffitnessusingtransposoninsertionsequencing
AT zhangyanjiaj artisthighresolutiongenomewideassessmentoffitnessusingtransposoninsertionsequencing
AT rubinericj artisthighresolutiongenomewideassessmentoffitnessusingtransposoninsertionsequencing
AT waldormatthewk artisthighresolutiongenomewideassessmentoffitnessusingtransposoninsertionsequencing