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Interactome of E. piscicida and grouper liver proteins reveals strategies of bacterial infection and host immune response
The occurrence of infectious diseases is related to heterogeneous protein interactions between a host and a microbe. Therefore, elucidating the host-pathogen interplay is essential. We previously revealed the protein interactome between Edwardsiella piscicida and fish gill cells, and the present stu...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5206647/ https://www.ncbi.nlm.nih.gov/pubmed/28045121 http://dx.doi.org/10.1038/srep39824 |
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author | Li, Hui Zhu, Qing-feng Peng, Xuan-xian Peng, Bo |
author_facet | Li, Hui Zhu, Qing-feng Peng, Xuan-xian Peng, Bo |
author_sort | Li, Hui |
collection | PubMed |
description | The occurrence of infectious diseases is related to heterogeneous protein interactions between a host and a microbe. Therefore, elucidating the host-pathogen interplay is essential. We previously revealed the protein interactome between Edwardsiella piscicida and fish gill cells, and the present study identified the protein interactome between E. piscicida and E. drummondhayi liver cells. E. drummondhayi liver cells and bacterial pull-down approaches were used to identify E. piscicida outer membrane proteins that bind to liver cells and fish liver cell proteins that interact with bacterial cells, respectively. Eight bacterial proteins and 11 fish proteins were characterized. Heterogeneous protein-protein interactions between these bacterial cells and fish liver cells were investigated through far-Western blotting and co-immunoprecipitation. A network was constructed based on 42 heterogeneous protein-protein interactions between seven bacterial proteins and 10 fish proteins. A comparison of the new interactome with the previously reported interactome showed that four bacterial proteins overlapped, whereas all of the identified fish proteins were new, suggesting a difference between bacterial tricks for evading host immunity and the host strategy for combating bacterial infection. Furthermore, these bacterial proteins were found to regulate the expression of host innate immune-related proteins. These findings indicate that the interactome contributes to bacterial infection and host immunity. |
format | Online Article Text |
id | pubmed-5206647 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-52066472017-01-04 Interactome of E. piscicida and grouper liver proteins reveals strategies of bacterial infection and host immune response Li, Hui Zhu, Qing-feng Peng, Xuan-xian Peng, Bo Sci Rep Article The occurrence of infectious diseases is related to heterogeneous protein interactions between a host and a microbe. Therefore, elucidating the host-pathogen interplay is essential. We previously revealed the protein interactome between Edwardsiella piscicida and fish gill cells, and the present study identified the protein interactome between E. piscicida and E. drummondhayi liver cells. E. drummondhayi liver cells and bacterial pull-down approaches were used to identify E. piscicida outer membrane proteins that bind to liver cells and fish liver cell proteins that interact with bacterial cells, respectively. Eight bacterial proteins and 11 fish proteins were characterized. Heterogeneous protein-protein interactions between these bacterial cells and fish liver cells were investigated through far-Western blotting and co-immunoprecipitation. A network was constructed based on 42 heterogeneous protein-protein interactions between seven bacterial proteins and 10 fish proteins. A comparison of the new interactome with the previously reported interactome showed that four bacterial proteins overlapped, whereas all of the identified fish proteins were new, suggesting a difference between bacterial tricks for evading host immunity and the host strategy for combating bacterial infection. Furthermore, these bacterial proteins were found to regulate the expression of host innate immune-related proteins. These findings indicate that the interactome contributes to bacterial infection and host immunity. Nature Publishing Group 2017-01-03 /pmc/articles/PMC5206647/ /pubmed/28045121 http://dx.doi.org/10.1038/srep39824 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Li, Hui Zhu, Qing-feng Peng, Xuan-xian Peng, Bo Interactome of E. piscicida and grouper liver proteins reveals strategies of bacterial infection and host immune response |
title | Interactome of E. piscicida and grouper liver proteins reveals strategies of bacterial infection and host immune response |
title_full | Interactome of E. piscicida and grouper liver proteins reveals strategies of bacterial infection and host immune response |
title_fullStr | Interactome of E. piscicida and grouper liver proteins reveals strategies of bacterial infection and host immune response |
title_full_unstemmed | Interactome of E. piscicida and grouper liver proteins reveals strategies of bacterial infection and host immune response |
title_short | Interactome of E. piscicida and grouper liver proteins reveals strategies of bacterial infection and host immune response |
title_sort | interactome of e. piscicida and grouper liver proteins reveals strategies of bacterial infection and host immune response |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5206647/ https://www.ncbi.nlm.nih.gov/pubmed/28045121 http://dx.doi.org/10.1038/srep39824 |
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