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The Escherichia coli O157:H7 bovine rumen fluid proteome reflects adaptive bacterial responses

BACKGROUND: To obtain insights into Escherichia coli O157:H7 (O157) survival mechanisms in the bovine rumen, we defined the growth characteristics and proteome of O157 cultured in rumen fluid (RF; pH 6.0-7.2 and low volatile fatty acid content) obtained from rumen-fistulated cattle fed low protein c...

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Autores principales: Kudva, Indira T, Stanton, Thaddeus B, Lippolis, John D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3936929/
https://www.ncbi.nlm.nih.gov/pubmed/24559513
http://dx.doi.org/10.1186/1471-2180-14-48
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author Kudva, Indira T
Stanton, Thaddeus B
Lippolis, John D
author_facet Kudva, Indira T
Stanton, Thaddeus B
Lippolis, John D
author_sort Kudva, Indira T
collection PubMed
description BACKGROUND: To obtain insights into Escherichia coli O157:H7 (O157) survival mechanisms in the bovine rumen, we defined the growth characteristics and proteome of O157 cultured in rumen fluid (RF; pH 6.0-7.2 and low volatile fatty acid content) obtained from rumen-fistulated cattle fed low protein content “maintenance diet” under diverse in vitro conditions. RESULTS: Bottom-up proteomics (LC-MS/MS) of whole cell-lysates of O157 cultured under anaerobic conditions in filter-sterilized RF (fRF; devoid of normal ruminal microbiota) and nutrient-depleted and filtered RF (dRF) resulted in an anaerobic O157 fRF-and dRF-proteome comprising 35 proteins functionally associated with cell structure, motility, transport, metabolism and regulation, but interestingly, not with O157 virulence. Shotgun proteomics-based analysis using isobaric tags for relative and absolute quantitation used to further study differential protein expression in unfiltered RF (uRF; RF containing normal rumen microbial flora) complemented these results. CONCLUSIONS: Our results indicate that in the rumen, the first anatomical compartment encountered by this human pathogen within the cattle gastrointestinal tract (GIT), O157 initiates a program of specific gene expression that enables it to adapt to the in vivo environment, and successfully transit to its colonization sites in the bovine GIT. Further experiments in vitro using uRF from animals fed different diets and with additional O157 strains, and in vivo using rumen-fistulated cattle will provide a comprehensive understanding of the adaptive mechanisms involved, and help direct evolution of novel modalities for blocking O157 infection of cattle.
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spelling pubmed-39369292014-02-28 The Escherichia coli O157:H7 bovine rumen fluid proteome reflects adaptive bacterial responses Kudva, Indira T Stanton, Thaddeus B Lippolis, John D BMC Microbiol Research Article BACKGROUND: To obtain insights into Escherichia coli O157:H7 (O157) survival mechanisms in the bovine rumen, we defined the growth characteristics and proteome of O157 cultured in rumen fluid (RF; pH 6.0-7.2 and low volatile fatty acid content) obtained from rumen-fistulated cattle fed low protein content “maintenance diet” under diverse in vitro conditions. RESULTS: Bottom-up proteomics (LC-MS/MS) of whole cell-lysates of O157 cultured under anaerobic conditions in filter-sterilized RF (fRF; devoid of normal ruminal microbiota) and nutrient-depleted and filtered RF (dRF) resulted in an anaerobic O157 fRF-and dRF-proteome comprising 35 proteins functionally associated with cell structure, motility, transport, metabolism and regulation, but interestingly, not with O157 virulence. Shotgun proteomics-based analysis using isobaric tags for relative and absolute quantitation used to further study differential protein expression in unfiltered RF (uRF; RF containing normal rumen microbial flora) complemented these results. CONCLUSIONS: Our results indicate that in the rumen, the first anatomical compartment encountered by this human pathogen within the cattle gastrointestinal tract (GIT), O157 initiates a program of specific gene expression that enables it to adapt to the in vivo environment, and successfully transit to its colonization sites in the bovine GIT. Further experiments in vitro using uRF from animals fed different diets and with additional O157 strains, and in vivo using rumen-fistulated cattle will provide a comprehensive understanding of the adaptive mechanisms involved, and help direct evolution of novel modalities for blocking O157 infection of cattle. BioMed Central 2014-02-21 /pmc/articles/PMC3936929/ /pubmed/24559513 http://dx.doi.org/10.1186/1471-2180-14-48 Text en Copyright © 2014 Kudva et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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
Kudva, Indira T
Stanton, Thaddeus B
Lippolis, John D
The Escherichia coli O157:H7 bovine rumen fluid proteome reflects adaptive bacterial responses
title The Escherichia coli O157:H7 bovine rumen fluid proteome reflects adaptive bacterial responses
title_full The Escherichia coli O157:H7 bovine rumen fluid proteome reflects adaptive bacterial responses
title_fullStr The Escherichia coli O157:H7 bovine rumen fluid proteome reflects adaptive bacterial responses
title_full_unstemmed The Escherichia coli O157:H7 bovine rumen fluid proteome reflects adaptive bacterial responses
title_short The Escherichia coli O157:H7 bovine rumen fluid proteome reflects adaptive bacterial responses
title_sort escherichia coli o157:h7 bovine rumen fluid proteome reflects adaptive bacterial responses
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3936929/
https://www.ncbi.nlm.nih.gov/pubmed/24559513
http://dx.doi.org/10.1186/1471-2180-14-48
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