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Proteomic and metabolomic profiles demonstrate variation among free-living and symbiotic vibrio fischeri biofilms
BACKGROUND: A number of bacterial species are capable of growing in various life history modes that enable their survival and persistence in both planktonic free-living stages as well as in biofilm communities. Mechanisms contributing to either planktonic cell or biofilm persistence and survival can...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4619220/ https://www.ncbi.nlm.nih.gov/pubmed/26494154 http://dx.doi.org/10.1186/s12866-015-0560-z |
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author | Chavez-Dozal, Alba Gorman, Clayton Nishiguchi, Michele K. |
author_facet | Chavez-Dozal, Alba Gorman, Clayton Nishiguchi, Michele K. |
author_sort | Chavez-Dozal, Alba |
collection | PubMed |
description | BACKGROUND: A number of bacterial species are capable of growing in various life history modes that enable their survival and persistence in both planktonic free-living stages as well as in biofilm communities. Mechanisms contributing to either planktonic cell or biofilm persistence and survival can be carefully delineated using multiple differential techniques (e.g., genomics and transcriptomics). In this study, we present both proteomic and metabolomic analyses of Vibrio fischeri biofilms, demonstrating the potential for combined differential studies for elucidating life-history switches important for establishing the mutualism through biofilm formation and host colonization. METHODS: The study used a metabolomics/proteomics or “meta-proteomics” approach, referring to the combined protein and metabolic data analysis that bridges the gap between phenotypic changes (planktonic cell to biofilm formation) with genotypic changes (reflected in protein/metabolic profiles). Our methods used protein shotgun construction, followed by liquid chromatography coupled with mass spectrometry (LC-MS) detection and quantification for both free-living and biofilm forming V. fischeri. RESULTS: We present a time-resolved picture of approximately 100 proteins (2D-PAGE and shotgun proteomics) and 200 metabolites that are present during the transition from planktonic growth to community biofilm formation. Proteins involved in stress response, DNA repair damage, and transport appeared to be highly expressed during the biofilm state. In addition, metabolites detected in biofilms correspond to components of the exopolysaccharide (EPS) matrix (sugars and glycerol-derived). Alterations in metabolic enzymes were paralleled by more pronounced changes in concentration of intermediates from the glycolysis pathway as well as several amino acids. CONCLUSIONS: This combined analysis of both types of information (proteins, metabolites) has provided a more complete picture of the biochemical processes of biofilm formation and what determines the switch between the two life history strategies. The reported findings have broad implications for Vibrio biofilm ecology, and mechanisms for successful survival in the host and environment. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12866-015-0560-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4619220 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46192202015-10-26 Proteomic and metabolomic profiles demonstrate variation among free-living and symbiotic vibrio fischeri biofilms Chavez-Dozal, Alba Gorman, Clayton Nishiguchi, Michele K. BMC Microbiol Research Article BACKGROUND: A number of bacterial species are capable of growing in various life history modes that enable their survival and persistence in both planktonic free-living stages as well as in biofilm communities. Mechanisms contributing to either planktonic cell or biofilm persistence and survival can be carefully delineated using multiple differential techniques (e.g., genomics and transcriptomics). In this study, we present both proteomic and metabolomic analyses of Vibrio fischeri biofilms, demonstrating the potential for combined differential studies for elucidating life-history switches important for establishing the mutualism through biofilm formation and host colonization. METHODS: The study used a metabolomics/proteomics or “meta-proteomics” approach, referring to the combined protein and metabolic data analysis that bridges the gap between phenotypic changes (planktonic cell to biofilm formation) with genotypic changes (reflected in protein/metabolic profiles). Our methods used protein shotgun construction, followed by liquid chromatography coupled with mass spectrometry (LC-MS) detection and quantification for both free-living and biofilm forming V. fischeri. RESULTS: We present a time-resolved picture of approximately 100 proteins (2D-PAGE and shotgun proteomics) and 200 metabolites that are present during the transition from planktonic growth to community biofilm formation. Proteins involved in stress response, DNA repair damage, and transport appeared to be highly expressed during the biofilm state. In addition, metabolites detected in biofilms correspond to components of the exopolysaccharide (EPS) matrix (sugars and glycerol-derived). Alterations in metabolic enzymes were paralleled by more pronounced changes in concentration of intermediates from the glycolysis pathway as well as several amino acids. CONCLUSIONS: This combined analysis of both types of information (proteins, metabolites) has provided a more complete picture of the biochemical processes of biofilm formation and what determines the switch between the two life history strategies. The reported findings have broad implications for Vibrio biofilm ecology, and mechanisms for successful survival in the host and environment. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12866-015-0560-z) contains supplementary material, which is available to authorized users. BioMed Central 2015-10-23 /pmc/articles/PMC4619220/ /pubmed/26494154 http://dx.doi.org/10.1186/s12866-015-0560-z Text en © Chavez-Dozal et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Chavez-Dozal, Alba Gorman, Clayton Nishiguchi, Michele K. Proteomic and metabolomic profiles demonstrate variation among free-living and symbiotic vibrio fischeri biofilms |
title | Proteomic and metabolomic profiles demonstrate variation among free-living and symbiotic vibrio fischeri biofilms |
title_full | Proteomic and metabolomic profiles demonstrate variation among free-living and symbiotic vibrio fischeri biofilms |
title_fullStr | Proteomic and metabolomic profiles demonstrate variation among free-living and symbiotic vibrio fischeri biofilms |
title_full_unstemmed | Proteomic and metabolomic profiles demonstrate variation among free-living and symbiotic vibrio fischeri biofilms |
title_short | Proteomic and metabolomic profiles demonstrate variation among free-living and symbiotic vibrio fischeri biofilms |
title_sort | proteomic and metabolomic profiles demonstrate variation among free-living and symbiotic vibrio fischeri biofilms |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4619220/ https://www.ncbi.nlm.nih.gov/pubmed/26494154 http://dx.doi.org/10.1186/s12866-015-0560-z |
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