Cargando…

The extracellular proteome of two Bifidobacterium species reveals different adaptation strategies to low iron conditions

BACKGROUND: Bifidobacteria are among the first anaerobic bacteria colonizing the gut. Bifidobacteria require iron for growth and their iron-sequestration mechanisms are important for their fitness and possibly inhibit enteropathogens. Here we used combined genomic and proteomic analyses to character...

Descripción completa

Detalles Bibliográficos
Autores principales: Vazquez-Gutierrez, Pamela, Stevens, Marc J. A., Gehrig, Peter, Barkow-Oesterreicher, Simon, Lacroix, Christophe, Chassard, Christophe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5219805/
https://www.ncbi.nlm.nih.gov/pubmed/28061804
http://dx.doi.org/10.1186/s12864-016-3472-x
_version_ 1782492528232103936
author Vazquez-Gutierrez, Pamela
Stevens, Marc J. A.
Gehrig, Peter
Barkow-Oesterreicher, Simon
Lacroix, Christophe
Chassard, Christophe
author_facet Vazquez-Gutierrez, Pamela
Stevens, Marc J. A.
Gehrig, Peter
Barkow-Oesterreicher, Simon
Lacroix, Christophe
Chassard, Christophe
author_sort Vazquez-Gutierrez, Pamela
collection PubMed
description BACKGROUND: Bifidobacteria are among the first anaerobic bacteria colonizing the gut. Bifidobacteria require iron for growth and their iron-sequestration mechanisms are important for their fitness and possibly inhibit enteropathogens. Here we used combined genomic and proteomic analyses to characterize adaptations to low iron conditions of B. kashiwanohense PV20-2 and B. pseudolongum PV8-2, 2 strains isolated from the feces of iron-deficient African infants and selected for their high iron-sequestering ability. RESULTS: Analyses of the genome contents revealed evolutionary adaptation to low iron conditions. A ferric and a ferrous iron operon encoding binding proteins and transporters were found in both strains. Remarkably, the ferric iron operon of B. pseudolongum PV8-2 is not found in other B. pseudolongum strains and likely acquired via horizontal gene transfer. The genome B. kashiwanohense PV20-2 harbors a unique region encoding genes putatively involved in siderophore production. Additionally, the secretomes of the two strains grown under low-iron conditions were analyzed using a combined genomic-proteomic approach. A ferric iron transporter was found in the secretome of B. pseudolongum PV8-2, while ferrous binding proteins were detected in the secretome of B. kashiwanohense PV20-2, suggesting different strategies to take up iron in the strains. In addition, proteins such as elongation factors, a glyceraldehyde-3-phosphate dehydrogenase, and the stress proteins GroEL and DnaK were identified in both secretomes. These proteins have been previously associated with adhesion of lactobacilli to epithelial cells. CONCLUSION: Analyses of the genome and secretome of B. kashiwanohense PV20-2 and B. pseudolongum PV8-2 revealed different adaptations to low iron conditions and identified extracellular proteins for iron transport. The identified extracellular proteins might be involved in competition for iron in the gastrointestinal tract. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-3472-x) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5219805
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-52198052017-01-11 The extracellular proteome of two Bifidobacterium species reveals different adaptation strategies to low iron conditions Vazquez-Gutierrez, Pamela Stevens, Marc J. A. Gehrig, Peter Barkow-Oesterreicher, Simon Lacroix, Christophe Chassard, Christophe BMC Genomics Research Article BACKGROUND: Bifidobacteria are among the first anaerobic bacteria colonizing the gut. Bifidobacteria require iron for growth and their iron-sequestration mechanisms are important for their fitness and possibly inhibit enteropathogens. Here we used combined genomic and proteomic analyses to characterize adaptations to low iron conditions of B. kashiwanohense PV20-2 and B. pseudolongum PV8-2, 2 strains isolated from the feces of iron-deficient African infants and selected for their high iron-sequestering ability. RESULTS: Analyses of the genome contents revealed evolutionary adaptation to low iron conditions. A ferric and a ferrous iron operon encoding binding proteins and transporters were found in both strains. Remarkably, the ferric iron operon of B. pseudolongum PV8-2 is not found in other B. pseudolongum strains and likely acquired via horizontal gene transfer. The genome B. kashiwanohense PV20-2 harbors a unique region encoding genes putatively involved in siderophore production. Additionally, the secretomes of the two strains grown under low-iron conditions were analyzed using a combined genomic-proteomic approach. A ferric iron transporter was found in the secretome of B. pseudolongum PV8-2, while ferrous binding proteins were detected in the secretome of B. kashiwanohense PV20-2, suggesting different strategies to take up iron in the strains. In addition, proteins such as elongation factors, a glyceraldehyde-3-phosphate dehydrogenase, and the stress proteins GroEL and DnaK were identified in both secretomes. These proteins have been previously associated with adhesion of lactobacilli to epithelial cells. CONCLUSION: Analyses of the genome and secretome of B. kashiwanohense PV20-2 and B. pseudolongum PV8-2 revealed different adaptations to low iron conditions and identified extracellular proteins for iron transport. The identified extracellular proteins might be involved in competition for iron in the gastrointestinal tract. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-3472-x) contains supplementary material, which is available to authorized users. BioMed Central 2017-01-06 /pmc/articles/PMC5219805/ /pubmed/28061804 http://dx.doi.org/10.1186/s12864-016-3472-x Text en © The Author(s). 2017 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
Vazquez-Gutierrez, Pamela
Stevens, Marc J. A.
Gehrig, Peter
Barkow-Oesterreicher, Simon
Lacroix, Christophe
Chassard, Christophe
The extracellular proteome of two Bifidobacterium species reveals different adaptation strategies to low iron conditions
title The extracellular proteome of two Bifidobacterium species reveals different adaptation strategies to low iron conditions
title_full The extracellular proteome of two Bifidobacterium species reveals different adaptation strategies to low iron conditions
title_fullStr The extracellular proteome of two Bifidobacterium species reveals different adaptation strategies to low iron conditions
title_full_unstemmed The extracellular proteome of two Bifidobacterium species reveals different adaptation strategies to low iron conditions
title_short The extracellular proteome of two Bifidobacterium species reveals different adaptation strategies to low iron conditions
title_sort extracellular proteome of two bifidobacterium species reveals different adaptation strategies to low iron conditions
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5219805/
https://www.ncbi.nlm.nih.gov/pubmed/28061804
http://dx.doi.org/10.1186/s12864-016-3472-x
work_keys_str_mv AT vazquezgutierrezpamela theextracellularproteomeoftwobifidobacteriumspeciesrevealsdifferentadaptationstrategiestolowironconditions
AT stevensmarcja theextracellularproteomeoftwobifidobacteriumspeciesrevealsdifferentadaptationstrategiestolowironconditions
AT gehrigpeter theextracellularproteomeoftwobifidobacteriumspeciesrevealsdifferentadaptationstrategiestolowironconditions
AT barkowoesterreichersimon theextracellularproteomeoftwobifidobacteriumspeciesrevealsdifferentadaptationstrategiestolowironconditions
AT lacroixchristophe theextracellularproteomeoftwobifidobacteriumspeciesrevealsdifferentadaptationstrategiestolowironconditions
AT chassardchristophe theextracellularproteomeoftwobifidobacteriumspeciesrevealsdifferentadaptationstrategiestolowironconditions
AT vazquezgutierrezpamela extracellularproteomeoftwobifidobacteriumspeciesrevealsdifferentadaptationstrategiestolowironconditions
AT stevensmarcja extracellularproteomeoftwobifidobacteriumspeciesrevealsdifferentadaptationstrategiestolowironconditions
AT gehrigpeter extracellularproteomeoftwobifidobacteriumspeciesrevealsdifferentadaptationstrategiestolowironconditions
AT barkowoesterreichersimon extracellularproteomeoftwobifidobacteriumspeciesrevealsdifferentadaptationstrategiestolowironconditions
AT lacroixchristophe extracellularproteomeoftwobifidobacteriumspeciesrevealsdifferentadaptationstrategiestolowironconditions
AT chassardchristophe extracellularproteomeoftwobifidobacteriumspeciesrevealsdifferentadaptationstrategiestolowironconditions