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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2017
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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. |
format | Online Article Text |
id | pubmed-5626973 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
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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