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Proteomics-based confirmation of protein expression and correction of annotation errors in the Brucella abortus genome

BACKGROUND: Brucellosis is a major bacterial zoonosis affecting domestic livestock and wild mammals, as well as humans around the globe. While conducting proteomics studies to better understand Brucella abortus virulence, we consolidated the proteomic data collected and compared it to publically ava...

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Autores principales: Lamontagne, Julie, Béland, Maxime, Forest, Anik, Côté-Martin, Alexandra, Nassif, Najib, Tomaki, Fadi, Moriyón, Ignacio, Moreno, Edgardo, Paramithiotis, Eustache
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2877026/
https://www.ncbi.nlm.nih.gov/pubmed/20462421
http://dx.doi.org/10.1186/1471-2164-11-300
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author Lamontagne, Julie
Béland, Maxime
Forest, Anik
Côté-Martin, Alexandra
Nassif, Najib
Tomaki, Fadi
Moriyón, Ignacio
Moreno, Edgardo
Paramithiotis, Eustache
author_facet Lamontagne, Julie
Béland, Maxime
Forest, Anik
Côté-Martin, Alexandra
Nassif, Najib
Tomaki, Fadi
Moriyón, Ignacio
Moreno, Edgardo
Paramithiotis, Eustache
author_sort Lamontagne, Julie
collection PubMed
description BACKGROUND: Brucellosis is a major bacterial zoonosis affecting domestic livestock and wild mammals, as well as humans around the globe. While conducting proteomics studies to better understand Brucella abortus virulence, we consolidated the proteomic data collected and compared it to publically available genomic data. RESULTS: The proteomic data was compiled from several independent comparative studies of Brucella abortus that used either outer membrane blebs, cytosols, or whole bacteria grown in media, as well as intracellular bacteria recovered at different times following macrophage infection. We identified a total of 621 bacterial proteins that were differentially expressed in a condition-specific manner. For 305 of these proteins we provide the first experimental evidence of their expression. Using a custom-built protein sequence database, we uncovered 7 annotation errors. We provide experimental evidence of expression of 5 genes that were originally annotated as non-expressed pseudogenes, as well as start site annotation errors for 2 other genes. CONCLUSIONS: An essential element for ensuring correct functional studies is the correspondence between reported genome sequences and subsequent proteomics studies. In this study, we have used proteomics evidence to confirm expression of multiple proteins previously considered to be putative, as well as correct annotation errors in the genome of Brucella abortus strain 2308.
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spelling pubmed-28770262010-05-27 Proteomics-based confirmation of protein expression and correction of annotation errors in the Brucella abortus genome Lamontagne, Julie Béland, Maxime Forest, Anik Côté-Martin, Alexandra Nassif, Najib Tomaki, Fadi Moriyón, Ignacio Moreno, Edgardo Paramithiotis, Eustache BMC Genomics Research Article BACKGROUND: Brucellosis is a major bacterial zoonosis affecting domestic livestock and wild mammals, as well as humans around the globe. While conducting proteomics studies to better understand Brucella abortus virulence, we consolidated the proteomic data collected and compared it to publically available genomic data. RESULTS: The proteomic data was compiled from several independent comparative studies of Brucella abortus that used either outer membrane blebs, cytosols, or whole bacteria grown in media, as well as intracellular bacteria recovered at different times following macrophage infection. We identified a total of 621 bacterial proteins that were differentially expressed in a condition-specific manner. For 305 of these proteins we provide the first experimental evidence of their expression. Using a custom-built protein sequence database, we uncovered 7 annotation errors. We provide experimental evidence of expression of 5 genes that were originally annotated as non-expressed pseudogenes, as well as start site annotation errors for 2 other genes. CONCLUSIONS: An essential element for ensuring correct functional studies is the correspondence between reported genome sequences and subsequent proteomics studies. In this study, we have used proteomics evidence to confirm expression of multiple proteins previously considered to be putative, as well as correct annotation errors in the genome of Brucella abortus strain 2308. BioMed Central 2010-05-12 /pmc/articles/PMC2877026/ /pubmed/20462421 http://dx.doi.org/10.1186/1471-2164-11-300 Text en Copyright ©2010 Lamontagne 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 cited.
spellingShingle Research Article
Lamontagne, Julie
Béland, Maxime
Forest, Anik
Côté-Martin, Alexandra
Nassif, Najib
Tomaki, Fadi
Moriyón, Ignacio
Moreno, Edgardo
Paramithiotis, Eustache
Proteomics-based confirmation of protein expression and correction of annotation errors in the Brucella abortus genome
title Proteomics-based confirmation of protein expression and correction of annotation errors in the Brucella abortus genome
title_full Proteomics-based confirmation of protein expression and correction of annotation errors in the Brucella abortus genome
title_fullStr Proteomics-based confirmation of protein expression and correction of annotation errors in the Brucella abortus genome
title_full_unstemmed Proteomics-based confirmation of protein expression and correction of annotation errors in the Brucella abortus genome
title_short Proteomics-based confirmation of protein expression and correction of annotation errors in the Brucella abortus genome
title_sort proteomics-based confirmation of protein expression and correction of annotation errors in the brucella abortus genome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2877026/
https://www.ncbi.nlm.nih.gov/pubmed/20462421
http://dx.doi.org/10.1186/1471-2164-11-300
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