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Proteomic analysis of the fish pathogen Flavobacterium columnare

BACKGROUND: Flavobacterium columnare causes columnaris disease in cultured and wild fish populations worldwide. Columnaris is the second most prevalent bacterial disease of commercial channel catfish industry in the United States. Despite its economic importance, little is known about the expressed...

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Autores principales: Dumpala, Pradeep R, Gülsoy, Nagihan, Lawrence, Mark L, Karsi, Attila
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2890538/
https://www.ncbi.nlm.nih.gov/pubmed/20525376
http://dx.doi.org/10.1186/1477-5956-8-26
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author Dumpala, Pradeep R
Gülsoy, Nagihan
Lawrence, Mark L
Karsi, Attila
author_facet Dumpala, Pradeep R
Gülsoy, Nagihan
Lawrence, Mark L
Karsi, Attila
author_sort Dumpala, Pradeep R
collection PubMed
description BACKGROUND: Flavobacterium columnare causes columnaris disease in cultured and wild fish populations worldwide. Columnaris is the second most prevalent bacterial disease of commercial channel catfish industry in the United States. Despite its economic importance, little is known about the expressed proteins and virulence mechanisms of F. columnare. Here, we report the first high throughput proteomic analysis of F. columnare using 2-D LC ESI MS/MS and 2-DE MALDI TOF/TOF MS. RESULTS: Proteins identified in this study and predicted from the draft F. columnare genome were clustered into functional groups using clusters of orthologous groups (COGs), and their subcellular locations were predicted. Possible functional relations among the identified proteins were determined using pathway analysis. The total number of unique F. columnare proteins identified using both 2-D LC and 2-DE approaches was 621, of which 10.95% (68) were identified by both methods, while 77.29% (480) and 11.76% (73) were unique in 2-D LC and 2-DE, respectively. COG groupings and subcellular localizations were similar between our data set and proteins predicted from the whole genome. Twenty eight pathways were significantly represented in our dataset (P < 0.05). CONCLUSION: Results from this study provide experimental evidence for many proteins that were predicted from the F. columnare genome annotation, and they should accelerate functional and comparative studies aimed at understanding virulence mechanisms of this important pathogen.
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spelling pubmed-28905382010-06-24 Proteomic analysis of the fish pathogen Flavobacterium columnare Dumpala, Pradeep R Gülsoy, Nagihan Lawrence, Mark L Karsi, Attila Proteome Sci Research BACKGROUND: Flavobacterium columnare causes columnaris disease in cultured and wild fish populations worldwide. Columnaris is the second most prevalent bacterial disease of commercial channel catfish industry in the United States. Despite its economic importance, little is known about the expressed proteins and virulence mechanisms of F. columnare. Here, we report the first high throughput proteomic analysis of F. columnare using 2-D LC ESI MS/MS and 2-DE MALDI TOF/TOF MS. RESULTS: Proteins identified in this study and predicted from the draft F. columnare genome were clustered into functional groups using clusters of orthologous groups (COGs), and their subcellular locations were predicted. Possible functional relations among the identified proteins were determined using pathway analysis. The total number of unique F. columnare proteins identified using both 2-D LC and 2-DE approaches was 621, of which 10.95% (68) were identified by both methods, while 77.29% (480) and 11.76% (73) were unique in 2-D LC and 2-DE, respectively. COG groupings and subcellular localizations were similar between our data set and proteins predicted from the whole genome. Twenty eight pathways were significantly represented in our dataset (P < 0.05). CONCLUSION: Results from this study provide experimental evidence for many proteins that were predicted from the F. columnare genome annotation, and they should accelerate functional and comparative studies aimed at understanding virulence mechanisms of this important pathogen. BioMed Central 2010-06-04 /pmc/articles/PMC2890538/ /pubmed/20525376 http://dx.doi.org/10.1186/1477-5956-8-26 Text en Copyright ©2010 Dumpala 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
Dumpala, Pradeep R
Gülsoy, Nagihan
Lawrence, Mark L
Karsi, Attila
Proteomic analysis of the fish pathogen Flavobacterium columnare
title Proteomic analysis of the fish pathogen Flavobacterium columnare
title_full Proteomic analysis of the fish pathogen Flavobacterium columnare
title_fullStr Proteomic analysis of the fish pathogen Flavobacterium columnare
title_full_unstemmed Proteomic analysis of the fish pathogen Flavobacterium columnare
title_short Proteomic analysis of the fish pathogen Flavobacterium columnare
title_sort proteomic analysis of the fish pathogen flavobacterium columnare
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2890538/
https://www.ncbi.nlm.nih.gov/pubmed/20525376
http://dx.doi.org/10.1186/1477-5956-8-26
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