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Proteome analysis reveals a role of rainbow trout lymphoid organs during Yersinia ruckeri infection process

Yersinia ruckeri is the causative agent of enteric redmouth disease in salmonids. Head kidney and spleen are major lymphoid organs of the teleost fish where antigen presentation and immune defense against microbes take place. We investigated proteome alteration in head kidney and spleen of the rainb...

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Autores principales: Kumar, Gokhlesh, Hummel, Karin, Noebauer, Katharina, Welch, Timothy J., Razzazi-Fazeli, Ebrahim, El-Matbouli, Mansour
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6143608/
https://www.ncbi.nlm.nih.gov/pubmed/30228307
http://dx.doi.org/10.1038/s41598-018-31982-6
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author Kumar, Gokhlesh
Hummel, Karin
Noebauer, Katharina
Welch, Timothy J.
Razzazi-Fazeli, Ebrahim
El-Matbouli, Mansour
author_facet Kumar, Gokhlesh
Hummel, Karin
Noebauer, Katharina
Welch, Timothy J.
Razzazi-Fazeli, Ebrahim
El-Matbouli, Mansour
author_sort Kumar, Gokhlesh
collection PubMed
description Yersinia ruckeri is the causative agent of enteric redmouth disease in salmonids. Head kidney and spleen are major lymphoid organs of the teleost fish where antigen presentation and immune defense against microbes take place. We investigated proteome alteration in head kidney and spleen of the rainbow trout following Y. ruckeri strains infection. Organs were analyzed after 3, 9 and 28 days post exposure with a shotgun proteomic approach. GO annotation and protein-protein interaction were predicted using bioinformatic tools. Thirty four proteins from head kidney and 85 proteins from spleen were found to be differentially expressed in rainbow trout during the Y. ruckeri infection process. These included lysosomal, antioxidant, metalloproteinase, cytoskeleton, tetraspanin, cathepsin B and c-type lectin receptor proteins. The findings of this study regarding the immune response at the protein level offer new insight into the systemic response to Y. ruckeri infection in rainbow trout. This proteomic data facilitate a better understanding of host-pathogen interactions and response of fish against Y. ruckeri biotype 1 and 2 strains. Protein-protein interaction analysis predicts carbon metabolism, ribosome and phagosome pathways in spleen of infected fish, which might be useful in understanding biological processes and further studies in the direction of pathways.
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spelling pubmed-61436082018-09-24 Proteome analysis reveals a role of rainbow trout lymphoid organs during Yersinia ruckeri infection process Kumar, Gokhlesh Hummel, Karin Noebauer, Katharina Welch, Timothy J. Razzazi-Fazeli, Ebrahim El-Matbouli, Mansour Sci Rep Article Yersinia ruckeri is the causative agent of enteric redmouth disease in salmonids. Head kidney and spleen are major lymphoid organs of the teleost fish where antigen presentation and immune defense against microbes take place. We investigated proteome alteration in head kidney and spleen of the rainbow trout following Y. ruckeri strains infection. Organs were analyzed after 3, 9 and 28 days post exposure with a shotgun proteomic approach. GO annotation and protein-protein interaction were predicted using bioinformatic tools. Thirty four proteins from head kidney and 85 proteins from spleen were found to be differentially expressed in rainbow trout during the Y. ruckeri infection process. These included lysosomal, antioxidant, metalloproteinase, cytoskeleton, tetraspanin, cathepsin B and c-type lectin receptor proteins. The findings of this study regarding the immune response at the protein level offer new insight into the systemic response to Y. ruckeri infection in rainbow trout. This proteomic data facilitate a better understanding of host-pathogen interactions and response of fish against Y. ruckeri biotype 1 and 2 strains. Protein-protein interaction analysis predicts carbon metabolism, ribosome and phagosome pathways in spleen of infected fish, which might be useful in understanding biological processes and further studies in the direction of pathways. Nature Publishing Group UK 2018-09-18 /pmc/articles/PMC6143608/ /pubmed/30228307 http://dx.doi.org/10.1038/s41598-018-31982-6 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Kumar, Gokhlesh
Hummel, Karin
Noebauer, Katharina
Welch, Timothy J.
Razzazi-Fazeli, Ebrahim
El-Matbouli, Mansour
Proteome analysis reveals a role of rainbow trout lymphoid organs during Yersinia ruckeri infection process
title Proteome analysis reveals a role of rainbow trout lymphoid organs during Yersinia ruckeri infection process
title_full Proteome analysis reveals a role of rainbow trout lymphoid organs during Yersinia ruckeri infection process
title_fullStr Proteome analysis reveals a role of rainbow trout lymphoid organs during Yersinia ruckeri infection process
title_full_unstemmed Proteome analysis reveals a role of rainbow trout lymphoid organs during Yersinia ruckeri infection process
title_short Proteome analysis reveals a role of rainbow trout lymphoid organs during Yersinia ruckeri infection process
title_sort proteome analysis reveals a role of rainbow trout lymphoid organs during yersinia ruckeri infection process
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6143608/
https://www.ncbi.nlm.nih.gov/pubmed/30228307
http://dx.doi.org/10.1038/s41598-018-31982-6
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