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Acetate metabolic requirement of avian pathogenic Escherichia coli promotes its intracellular proliferation within macrophage
Avian pathogenic Escherichia coli (APEC) is a facultative intracellular pathogen, and intracellular persistence in macrophages is essential for APEC extraintestinal dissemination. Until now, there is still no systematic interpretation of APEC intracellular proliferation. Intracellular survival facto...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6498577/ https://www.ncbi.nlm.nih.gov/pubmed/31046828 http://dx.doi.org/10.1186/s13567-019-0650-2 |
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author | Zhuge, Xiangkai Sun, Yu Jiang, Min Wang, Juanfang Tang, Fang Xue, Feng Ren, Jianluan Zhu, Weiyun Dai, Jianjun |
author_facet | Zhuge, Xiangkai Sun, Yu Jiang, Min Wang, Juanfang Tang, Fang Xue, Feng Ren, Jianluan Zhu, Weiyun Dai, Jianjun |
author_sort | Zhuge, Xiangkai |
collection | PubMed |
description | Avian pathogenic Escherichia coli (APEC) is a facultative intracellular pathogen, and intracellular persistence in macrophages is essential for APEC extraintestinal dissemination. Until now, there is still no systematic interpretation of APEC intracellular proliferation. Intracellular survival factors, especially involved in pathometabolism, need to be further revealed. Acetate plays critical roles in supporting energy homeostasis and acts as a metabolic signal in the inflammatory response of eukaryotes. In this study, we identified that APEC acs-yjcH-actP operon, encoding acetate assimilation system, presented the host-induced transcription during its proliferation in macrophages. Our result showed that this acetate assimilation system acted as a novel intracellular survival factor to promote APEC replication within macrophages. Furthermore, deletion of acs-yjcH-actP operon in APEC decreased its cytotoxic level to macrophages. qRT-PCR results showed that the production of pro-inflammatory cytokines (IL-1β, IL-6, IL-8, IL-12β, and TNF-α) and iNOS in FY26∆acs-yjcH-actP infected macrophages were obviously down-regulated compared to that in wild-type FY26 infected cells. Deletion of actP/yjcH/acs genes attenuated APEC virulence and colonization capability in avian lungs in vivo for colibacillosis infection models. And acetate assimilation system acted as a virulence factor and conferred a fitness advantage during APEC early colonization. Taken together, our research unravelled the metabolic requirement of APEC intracellular survival/replication within macrophages, and acetate metabolic requirement acted as an important strategy of APEC pathometabolism. The intracellular acetate consumption during facultative intracellular bacteria replication within macrophages promoted immunomodulatory disorders, resulting in excessively pro-inflammatory responses of host macrophages. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13567-019-0650-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6498577 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-64985772019-05-09 Acetate metabolic requirement of avian pathogenic Escherichia coli promotes its intracellular proliferation within macrophage Zhuge, Xiangkai Sun, Yu Jiang, Min Wang, Juanfang Tang, Fang Xue, Feng Ren, Jianluan Zhu, Weiyun Dai, Jianjun Vet Res Research Article Avian pathogenic Escherichia coli (APEC) is a facultative intracellular pathogen, and intracellular persistence in macrophages is essential for APEC extraintestinal dissemination. Until now, there is still no systematic interpretation of APEC intracellular proliferation. Intracellular survival factors, especially involved in pathometabolism, need to be further revealed. Acetate plays critical roles in supporting energy homeostasis and acts as a metabolic signal in the inflammatory response of eukaryotes. In this study, we identified that APEC acs-yjcH-actP operon, encoding acetate assimilation system, presented the host-induced transcription during its proliferation in macrophages. Our result showed that this acetate assimilation system acted as a novel intracellular survival factor to promote APEC replication within macrophages. Furthermore, deletion of acs-yjcH-actP operon in APEC decreased its cytotoxic level to macrophages. qRT-PCR results showed that the production of pro-inflammatory cytokines (IL-1β, IL-6, IL-8, IL-12β, and TNF-α) and iNOS in FY26∆acs-yjcH-actP infected macrophages were obviously down-regulated compared to that in wild-type FY26 infected cells. Deletion of actP/yjcH/acs genes attenuated APEC virulence and colonization capability in avian lungs in vivo for colibacillosis infection models. And acetate assimilation system acted as a virulence factor and conferred a fitness advantage during APEC early colonization. Taken together, our research unravelled the metabolic requirement of APEC intracellular survival/replication within macrophages, and acetate metabolic requirement acted as an important strategy of APEC pathometabolism. The intracellular acetate consumption during facultative intracellular bacteria replication within macrophages promoted immunomodulatory disorders, resulting in excessively pro-inflammatory responses of host macrophages. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13567-019-0650-2) contains supplementary material, which is available to authorized users. BioMed Central 2019-05-02 2019 /pmc/articles/PMC6498577/ /pubmed/31046828 http://dx.doi.org/10.1186/s13567-019-0650-2 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 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 Zhuge, Xiangkai Sun, Yu Jiang, Min Wang, Juanfang Tang, Fang Xue, Feng Ren, Jianluan Zhu, Weiyun Dai, Jianjun Acetate metabolic requirement of avian pathogenic Escherichia coli promotes its intracellular proliferation within macrophage |
title | Acetate metabolic requirement of avian pathogenic Escherichia coli promotes its intracellular proliferation within macrophage |
title_full | Acetate metabolic requirement of avian pathogenic Escherichia coli promotes its intracellular proliferation within macrophage |
title_fullStr | Acetate metabolic requirement of avian pathogenic Escherichia coli promotes its intracellular proliferation within macrophage |
title_full_unstemmed | Acetate metabolic requirement of avian pathogenic Escherichia coli promotes its intracellular proliferation within macrophage |
title_short | Acetate metabolic requirement of avian pathogenic Escherichia coli promotes its intracellular proliferation within macrophage |
title_sort | acetate metabolic requirement of avian pathogenic escherichia coli promotes its intracellular proliferation within macrophage |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6498577/ https://www.ncbi.nlm.nih.gov/pubmed/31046828 http://dx.doi.org/10.1186/s13567-019-0650-2 |
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