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Itaconic acid inhibits growth of a pathogenic marine Vibrio strain: A metabolomics approach
The antimicrobial role of itaconic acid (ITA) has been recently discovered in mammalian cells. In our previous studies, we discovered that marine molluscs biosynthesise substantial quantities of ITA when exposed to marine pathogens, but its antimicrobial function to Vibrio bacteria is currently unkn...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6459830/ https://www.ncbi.nlm.nih.gov/pubmed/30976014 http://dx.doi.org/10.1038/s41598-019-42315-6 |
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author | Nguyen, Thao Van Alfaro, Andrea C. Young, Tim Green, Saras Zarate, Erica Merien, Fabrice |
author_facet | Nguyen, Thao Van Alfaro, Andrea C. Young, Tim Green, Saras Zarate, Erica Merien, Fabrice |
author_sort | Nguyen, Thao Van |
collection | PubMed |
description | The antimicrobial role of itaconic acid (ITA) has been recently discovered in mammalian cells. In our previous studies, we discovered that marine molluscs biosynthesise substantial quantities of ITA when exposed to marine pathogens, but its antimicrobial function to Vibrio bacteria is currently unknown. Thus, in this study, we used an untargeted gas chromatography–mass spectrometry (GC-MS) platform to identify metabolic changes of Vibrio sp. DO1 (V. corallyliticus/neptunius-like isolate) caused by ITA exposure. Vibrio sp. DO1 was cultured in Luria-Bertani broth supplemented with 3 mM sodium acetate and with different concentrations of ITA (0, 3 and 6 mM) for 24 h. The results showed that ITA completely inhibited Vibrio sp. growth at 6 mM and partially inhibited the bacterial growth at 3 mM. A principal component analysis (PCA) revealed a clear separation between metabolite profiles of Vibrio sp. DO1 in the 3 mM ITA treatment and the control, which were different in 25 metabolites. Among the altered metabolites, the accumulation of glyoxylic acid and other metabolites in glyoxylate cycle (cis-aconitic acid, isocitric acid and fumaric acid) together with the increase of isocitrate lyase (ICL) activity in the 3 mM ITA treatment compared to the control suggest that ITA inhibited Vibrio sp. growth via disruption of central carbon metabolism. |
format | Online Article Text |
id | pubmed-6459830 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64598302019-04-16 Itaconic acid inhibits growth of a pathogenic marine Vibrio strain: A metabolomics approach Nguyen, Thao Van Alfaro, Andrea C. Young, Tim Green, Saras Zarate, Erica Merien, Fabrice Sci Rep Article The antimicrobial role of itaconic acid (ITA) has been recently discovered in mammalian cells. In our previous studies, we discovered that marine molluscs biosynthesise substantial quantities of ITA when exposed to marine pathogens, but its antimicrobial function to Vibrio bacteria is currently unknown. Thus, in this study, we used an untargeted gas chromatography–mass spectrometry (GC-MS) platform to identify metabolic changes of Vibrio sp. DO1 (V. corallyliticus/neptunius-like isolate) caused by ITA exposure. Vibrio sp. DO1 was cultured in Luria-Bertani broth supplemented with 3 mM sodium acetate and with different concentrations of ITA (0, 3 and 6 mM) for 24 h. The results showed that ITA completely inhibited Vibrio sp. growth at 6 mM and partially inhibited the bacterial growth at 3 mM. A principal component analysis (PCA) revealed a clear separation between metabolite profiles of Vibrio sp. DO1 in the 3 mM ITA treatment and the control, which were different in 25 metabolites. Among the altered metabolites, the accumulation of glyoxylic acid and other metabolites in glyoxylate cycle (cis-aconitic acid, isocitric acid and fumaric acid) together with the increase of isocitrate lyase (ICL) activity in the 3 mM ITA treatment compared to the control suggest that ITA inhibited Vibrio sp. growth via disruption of central carbon metabolism. Nature Publishing Group UK 2019-04-11 /pmc/articles/PMC6459830/ /pubmed/30976014 http://dx.doi.org/10.1038/s41598-019-42315-6 Text en © The Author(s) 2019 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 Nguyen, Thao Van Alfaro, Andrea C. Young, Tim Green, Saras Zarate, Erica Merien, Fabrice Itaconic acid inhibits growth of a pathogenic marine Vibrio strain: A metabolomics approach |
title | Itaconic acid inhibits growth of a pathogenic marine Vibrio strain: A metabolomics approach |
title_full | Itaconic acid inhibits growth of a pathogenic marine Vibrio strain: A metabolomics approach |
title_fullStr | Itaconic acid inhibits growth of a pathogenic marine Vibrio strain: A metabolomics approach |
title_full_unstemmed | Itaconic acid inhibits growth of a pathogenic marine Vibrio strain: A metabolomics approach |
title_short | Itaconic acid inhibits growth of a pathogenic marine Vibrio strain: A metabolomics approach |
title_sort | itaconic acid inhibits growth of a pathogenic marine vibrio strain: a metabolomics approach |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6459830/ https://www.ncbi.nlm.nih.gov/pubmed/30976014 http://dx.doi.org/10.1038/s41598-019-42315-6 |
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