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      Malate enhances survival of zebrafish against Vibrio alginolyticus infection in the same manner as taurine

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          ABSTRACT

          Development of low-cost and eco-friendly approaches to fight bacterial pathogens is especially needed in aquaculture. We previously showed that exogenous malate reprograms zebrafish’s metabolome to potentiate zebrafish survival against Vibrio alginolyticus infection. However, the underlying mechanism is unknown. Here, we use GC-MS based metabolomics to identify the malate-triggered metabolic shift. An activated TCA cycle and elevated taurine are identified as the key metabolic pathways and the most crucial biomarker of the reprogrammed metabolome, respectively. Taurine elevation is attributed to the activated TCA cycle, which is further supported by the increased expression of genes in the metabolic pathway of taurine biosynthesis from the isocitrate of the TCA cycle to taurine. Exogenous taurine increases the survival of zebrafish against V. alginolyticus infection as malate did. Moreover, exogenous taurine and malate regulate the expression of innate immunity genes and promote the generation of reactive oxygen species and nitrogen oxide in a similar way. The two metabolites can alleviate the excessive immune response to bacterial challenge, which protects fish from bacterial infection. These results indicate that malate enhances the survival of zebrafish to V. alginolyticus infection via taurine. Thus, our study highlights a metabolic approach to enhance a host’s ability to fight bacterial infection.

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          Bacterial Metabolism and Antibiotic Efficacy

          Summary Antibiotics target energy-consuming processes. As such, perturbations to bacterial metabolic homeostasis are significant consequences of treatment. Here, we describe three postulates that collectively define antibiotic efficacy in the context of bacterial metabolism: (1) antibiotics alter the metabolic state of bacteria, which contributes to the resulting death or stasis; (2) the metabolic state of bacteria influences their susceptibility to antibiotics; and (3) antibiotic efficacy can be enhanced by altering the metabolic state of bacteria. Altogether, we aim to emphasize the close relationship between bacterial metabolism and antibiotic efficacy as well as propose areas of exploration to develop novel antibiotics that optimally exploit bacterial metabolic networks.
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            Exogenous alanine and/or glucose plus kanamycin kills antibiotic-resistant bacteria.

            Multidrug-resistant bacteria are an increasingly serious threat to human and animal health. However, novel drugs that can manage infections by multidrug-resistant bacteria have proved elusive. Here we show that glucose and alanine abundances are greatly suppressed in kanamycin-resistant Edwardsiella tarda by GC-MS-based metabolomics. Exogenous alanine or glucose restores susceptibility of multidrug-resistant E. tarda to killing by kanamycin, demonstrating an approach to killing multidrug-resistant bacteria. The mechanism underlying this approach is that exogenous glucose or alanine promotes the TCA cycle by substrate activation, which in turn increases production of NADH and proton motive force and stimulates uptake of antibiotic. Similar results are obtained with other Gram-negative bacteria (Vibrio parahaemolyticus, Klebsiella pneumoniae, Pseudomonas aeruginosa) and Gram-positive bacterium (Staphylococcus aureus), and the results are also reproduced in a mouse model for urinary tract infection. This study establishes a functional metabolomics-based strategy to manage infection by antibiotic-resistant bacteria.
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              iPath2.0: interactive pathway explorer

              iPath2.0 is a web-based tool (http://pathways.embl.de) for the visualization and analysis of cellular pathways. Its primary map summarizes the metabolism in biological systems as annotated to date. Nodes in the map correspond to various chemical compounds and edges represent series of enzymatic reactions. In two other maps, iPath2.0 provides an overview of secondary metabolite biosynthesis and a hand-picked selection of important regulatory pathways and other functional modules, allowing a more general overview of protein functions in a genome or metagenome. iPath2.0′s main interface is an interactive Flash-based viewer, which allows users to easily navigate and explore the complex pathway maps. In addition to the default pre-computed overview maps, iPath offers several data mapping tools. Users can upload various types of data and completely customize all nodes and edges of iPath2.0′s maps. These customized maps give users an intuitive overview of their own data, guiding the analysis of various genomics and metagenomics projects.
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                Author and article information

                Journal
                Virulence
                Virulence
                KVIR
                kvir20
                Virulence
                Taylor & Francis
                2150-5594
                2150-5608
                2020
                21 April 2020
                21 April 2020
                : 11
                : 1
                : 349-364
                Affiliations
                [a ]Center for Proteomics and Metabolomics, State Key Laboratory of Biocontrol, Guangdong Province Key Laboratory for Pharmaceutical Functional Genes, School of Life Sciences, Sun Yat-sen University, University City , Guangzhou, People’s Republic of China
                [b ]Laboratory for Marine Fisheries Science and Food Production Processes, National Laboratory for Marine Science and Technology , Qingdao, China
                [c ]Tibet Vocational Technical College , Lhasha, People’s Republic of China
                [d ]Third Affiliated Hospital of Sun Yat-sen University , Guangzhou 510630, People’s Republic of China
                Author notes
                [*]

                These authors contributed equally to this work.

                Author information
                http://orcid.org/0000-0002-2770-5364
                http://orcid.org/0000-0002-0200-1395
                http://orcid.org/0000-0003-2600-4838
                Article
                1750123
                10.1080/21505594.2020.1750123
                7199751
                32316833
                9688b801-c8b4-473c-8db8-801720e803c9
                © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 4 November 2019
                : 20 January 2020
                : 3 February 2020
                Page count
                Figures: 7, References: 65, Pages: 16
                Funding
                Funded by: NSFC project
                Award ID: U1701235
                Funded by: Pilot National Laboratory for Marine Science and Technology
                Award ID: BH-A10
                Funded by: Science and technology plan project of Guangzhou
                Award ID: 201904020042
                Funded by: National Key Research and Development Program of China
                Award ID: 2018YFD0900504
                This work was sponsored by grants from the National Key Research and Development Program of China (2018YFD0900504), NSFC project (U1701235), Pilot National Laboratory for Marine Science and Technology (Qingdao) (BH-A10) and Science and technology plan project of Guangzhou (201904020042).
                Categories
                Research Paper

                Infectious disease & Microbiology
                taurine,malate,reprogramming metabolomics,vibrio alginolyticus,aquaculture,zebrafish

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