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Time-Resolved Transposon Insertion Sequencing Reveals Genome-Wide Fitness Dynamics during Infection

Transposon insertion sequencing (TIS) is a powerful high-throughput genetic technique that is transforming functional genomics in prokaryotes, because it enables genome-wide mapping of the determinants of fitness. However, current approaches for analyzing TIS data assume that selective pressures are...

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Autores principales: Yang, Guanhua, Billings, Gabriel, Hubbard, Troy P., Park, Joseph S., Yin Leung, Ka, Liu, Qin, Davis, Brigid M., Zhang, Yuanxing, Wang, Qiyao, Waldor, Matthew K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5626973/
https://www.ncbi.nlm.nih.gov/pubmed/28974620
http://dx.doi.org/10.1128/mBio.01581-17
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author Yang, Guanhua
Billings, Gabriel
Hubbard, Troy P.
Park, Joseph S.
Yin Leung, Ka
Liu, Qin
Davis, Brigid M.
Zhang, Yuanxing
Wang, Qiyao
Waldor, Matthew K.
author_facet Yang, Guanhua
Billings, Gabriel
Hubbard, Troy P.
Park, Joseph S.
Yin Leung, Ka
Liu, Qin
Davis, Brigid M.
Zhang, Yuanxing
Wang, Qiyao
Waldor, Matthew K.
author_sort Yang, Guanhua
collection PubMed
description Transposon insertion sequencing (TIS) is a powerful high-throughput genetic technique that is transforming functional genomics in prokaryotes, because it enables genome-wide mapping of the determinants of fitness. However, current approaches for analyzing TIS data assume that selective pressures are constant over time and thus do not yield information regarding changes in the genetic requirements for growth in dynamic environments (e.g., during infection). Here, we describe structured analysis of TIS data collected as a time series, termed pattern analysis of conditional essentiality (PACE). From a temporal series of TIS data, PACE derives a quantitative assessment of each mutant’s fitness over the course of an experiment and identifies mutants with related fitness profiles. In so doing, PACE circumvents major limitations of existing methodologies, specifically the need for artificial effect size thresholds and enumeration of bacterial population expansion. We used PACE to analyze TIS samples of Edwardsiella piscicida (a fish pathogen) collected over a 2-week infection period from a natural host (the flatfish turbot). PACE uncovered more genes that affect E. piscicida’s fitness in vivo than were detected using a cutoff at a terminal sampling point, and it identified subpopulations of mutants with distinct fitness profiles, one of which informed the design of new live vaccine candidates. Overall, PACE enables efficient mining of time series TIS data and enhances the power and sensitivity of TIS-based analyses.
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spelling pubmed-56269732017-10-04 Time-Resolved Transposon Insertion Sequencing Reveals Genome-Wide Fitness Dynamics during Infection Yang, Guanhua Billings, Gabriel Hubbard, Troy P. Park, Joseph S. Yin Leung, Ka Liu, Qin Davis, Brigid M. Zhang, Yuanxing Wang, Qiyao Waldor, Matthew K. mBio Research Article Transposon insertion sequencing (TIS) is a powerful high-throughput genetic technique that is transforming functional genomics in prokaryotes, because it enables genome-wide mapping of the determinants of fitness. However, current approaches for analyzing TIS data assume that selective pressures are constant over time and thus do not yield information regarding changes in the genetic requirements for growth in dynamic environments (e.g., during infection). Here, we describe structured analysis of TIS data collected as a time series, termed pattern analysis of conditional essentiality (PACE). From a temporal series of TIS data, PACE derives a quantitative assessment of each mutant’s fitness over the course of an experiment and identifies mutants with related fitness profiles. In so doing, PACE circumvents major limitations of existing methodologies, specifically the need for artificial effect size thresholds and enumeration of bacterial population expansion. We used PACE to analyze TIS samples of Edwardsiella piscicida (a fish pathogen) collected over a 2-week infection period from a natural host (the flatfish turbot). PACE uncovered more genes that affect E. piscicida’s fitness in vivo than were detected using a cutoff at a terminal sampling point, and it identified subpopulations of mutants with distinct fitness profiles, one of which informed the design of new live vaccine candidates. Overall, PACE enables efficient mining of time series TIS data and enhances the power and sensitivity of TIS-based analyses. American Society for Microbiology 2017-10-03 /pmc/articles/PMC5626973/ /pubmed/28974620 http://dx.doi.org/10.1128/mBio.01581-17 Text en Copyright © 2017 Yang et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Yang, Guanhua
Billings, Gabriel
Hubbard, Troy P.
Park, Joseph S.
Yin Leung, Ka
Liu, Qin
Davis, Brigid M.
Zhang, Yuanxing
Wang, Qiyao
Waldor, Matthew K.
Time-Resolved Transposon Insertion Sequencing Reveals Genome-Wide Fitness Dynamics during Infection
title Time-Resolved Transposon Insertion Sequencing Reveals Genome-Wide Fitness Dynamics during Infection
title_full Time-Resolved Transposon Insertion Sequencing Reveals Genome-Wide Fitness Dynamics during Infection
title_fullStr Time-Resolved Transposon Insertion Sequencing Reveals Genome-Wide Fitness Dynamics during Infection
title_full_unstemmed Time-Resolved Transposon Insertion Sequencing Reveals Genome-Wide Fitness Dynamics during Infection
title_short Time-Resolved Transposon Insertion Sequencing Reveals Genome-Wide Fitness Dynamics during Infection
title_sort time-resolved transposon insertion sequencing reveals genome-wide fitness dynamics during infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5626973/
https://www.ncbi.nlm.nih.gov/pubmed/28974620
http://dx.doi.org/10.1128/mBio.01581-17
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