The methylglyoxal pathway is a sink for glutathione in Salmonella experiencing oxidative stress
Salmonella suffer the cytotoxicity of reactive oxygen species generated by the phagocyte NADPH oxidase in the innate host response. Periplasmic superoxide dismutases, catalases and hydroperoxidases detoxify superoxide and hydrogen peroxide (H2O2) synthesized in the respiratory burst of phagocytic ce...
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Published in | PLoS pathogens Vol. 19; no. 6; p. e1011441 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
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01.06.2023
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Abstract | Salmonella suffer the cytotoxicity of reactive oxygen species generated by the phagocyte NADPH oxidase in the innate host response. Periplasmic superoxide dismutases, catalases and hydroperoxidases detoxify superoxide and hydrogen peroxide (H2O2) synthesized in the respiratory burst of phagocytic cells. Glutathione also helps Salmonella combat the phagocyte NADPH oxidase; however, the molecular mechanisms by which this low-molecular-weight thiol promotes resistance of Salmonella to oxidative stress are currently unknown. We report herein that Salmonella undergoing oxidative stress transcriptionally and functionally activate the methylglyoxal pathway that branches off from glycolysis. Activation of the methylglyoxal pathway consumes a substantial proportion of the glutathione reducing power in Salmonella following exposure to H2O2. The methylglyoxal pathway enables Salmonella to balance glucose utilization with aerobic respiratory outputs. Salmonella take advantage of the metabolic flexibility associated with the glutathione-consuming methylglyoxal pathway to resist reactive oxygen species generated by the enzymatic activity of the phagocyte NADPH oxidase in macrophages and mice. Taken together, glutathione fosters oxidative stress resistance in Salmonella against the antimicrobial actions of the phagocyte NADPH oxidase by promoting the methylglyoxal pathway, an offshoot metabolic adaptation of glycolysis. |
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AbstractList | Salmonella suffer the cytotoxicity of reactive oxygen species generated by the phagocyte NADPH oxidase in the innate host response. Periplasmic superoxide dismutases, catalases and hydroperoxidases detoxify superoxide and hydrogen peroxide (H2O2) synthesized in the respiratory burst of phagocytic cells. Glutathione also helps Salmonella combat the phagocyte NADPH oxidase; however, the molecular mechanisms by which this low-molecular-weight thiol promotes resistance of Salmonella to oxidative stress are currently unknown. We report herein that Salmonella undergoing oxidative stress transcriptionally and functionally activate the methylglyoxal pathway that branches off from glycolysis. Activation of the methylglyoxal pathway consumes a substantial proportion of the glutathione reducing power in Salmonella following exposure to H2O2. The methylglyoxal pathway enables Salmonella to balance glucose utilization with aerobic respiratory outputs. Salmonella take advantage of the metabolic flexibility associated with the glutathione-consuming methylglyoxal pathway to resist reactive oxygen species generated by the enzymatic activity of the phagocyte NADPH oxidase in macrophages and mice. Taken together, glutathione fosters oxidative stress resistance in Salmonella against the antimicrobial actions of the phagocyte NADPH oxidase by promoting the methylglyoxal pathway, an offshoot metabolic adaptation of glycolysis. Salmonella suffer the cytotoxicity of reactive oxygen species generated by the phagocyte NADPH oxidase in the innate host response. Periplasmic superoxide dismutases, catalases and hydroperoxidases detoxify superoxide and hydrogen peroxide (H 2 O 2 ) synthesized in the respiratory burst of phagocytic cells. Glutathione also helps Salmonella combat the phagocyte NADPH oxidase; however, the molecular mechanisms by which this low-molecular-weight thiol promotes resistance of Salmonella to oxidative stress are currently unknown. We report herein that Salmonella undergoing oxidative stress transcriptionally and functionally activate the methylglyoxal pathway that branches off from glycolysis. Activation of the methylglyoxal pathway consumes a substantial proportion of the glutathione reducing power in Salmonella following exposure to H 2 O 2 . The methylglyoxal pathway enables Salmonella to balance glucose utilization with aerobic respiratory outputs. Salmonella take advantage of the metabolic flexibility associated with the glutathione-consuming methylglyoxal pathway to resist reactive oxygen species generated by the enzymatic activity of the phagocyte NADPH oxidase in macrophages and mice. Taken together, glutathione fosters oxidative stress resistance in Salmonella against the antimicrobial actions of the phagocyte NADPH oxidase by promoting the methylglyoxal pathway, an offshoot metabolic adaptation of glycolysis. Low-molecular-weight thiols such as the tripeptide glutathione are essential components of the antioxidant arsenal of phylogenetically diverse organisms. Salmonella undergoing peroxide stress suffer a dramatic diminution in the pool of reduced glutathione. However, drops in glutathione reducing power are not paralleled with a buildup of oxidized glutathione that would be expected by direct oxidation of the tripeptide by H 2 O 2 . The involvement of glutathione synthetase, but not glutathione oxidoreductase that reduces oxidized glutathione, casts further doubt on the role of this low-molecular-weight thiol as scavenger of reactive oxygen species in Salmonella pathogenesis. Our investigations herein show that Salmonella sustaining oxidative stress consume large amounts of glutathione in the methylglyoxal pathway that is activated as overflow metabolism is favored during periods of oxidative stress. The lactoylglutathione hydrolase activity of glyoxalase II in the methylglyoxal pathway allows Salmonella to grow in glucose, while simultaneously fostering aerobic respiration. In conclusion, the contribution of glutathione to the resistance of Salmonella to oxidative stress mostly stems from the electrophilic detoxification of aldehyde byproducts of metabolism rather than serving as a scavenger of reactive oxygen species via direct nucleophilic attack of H 2 O 2 peroxo linkage. Salmonella suffer the cytotoxicity of reactive oxygen species generated by the phagocyte NADPH oxidase in the innate host response. Periplasmic superoxide dismutases, catalases and hydroperoxidases detoxify superoxide and hydrogen peroxide (H.sub.2 O.sub.2) synthesized in the respiratory burst of phagocytic cells. Glutathione also helps Salmonella combat the phagocyte NADPH oxidase; however, the molecular mechanisms by which this low-molecular-weight thiol promotes resistance of Salmonella to oxidative stress are currently unknown. We report herein that Salmonella undergoing oxidative stress transcriptionally and functionally activate the methylglyoxal pathway that branches off from glycolysis. Activation of the methylglyoxal pathway consumes a substantial proportion of the glutathione reducing power in Salmonella following exposure to H.sub.2 O.sub.2 . The methylglyoxal pathway enables Salmonella to balance glucose utilization with aerobic respiratory outputs. Salmonella take advantage of the metabolic flexibility associated with the glutathione-consuming methylglyoxal pathway to resist reactive oxygen species generated by the enzymatic activity of the phagocyte NADPH oxidase in macrophages and mice. Taken together, glutathione fosters oxidative stress resistance in Salmonella against the antimicrobial actions of the phagocyte NADPH oxidase by promoting the methylglyoxal pathway, an offshoot metabolic adaptation of glycolysis. Salmonella suffer the cytotoxicity of reactive oxygen species generated by the phagocyte NADPH oxidase in the innate host response. Periplasmic superoxide dismutases, catalases and hydroperoxidases detoxify superoxide and hydrogen peroxide (H 2 O 2 ) synthesized in the respiratory burst of phagocytic cells. Glutathione also helps Salmonella combat the phagocyte NADPH oxidase; however, the molecular mechanisms by which this low-molecular-weight thiol promotes resistance of Salmonella to oxidative stress are currently unknown. We report herein that Salmonella undergoing oxidative stress transcriptionally and functionally activate the methylglyoxal pathway that branches off from glycolysis. Activation of the methylglyoxal pathway consumes a substantial proportion of the glutathione reducing power in Salmonella following exposure to H 2 O 2 . The methylglyoxal pathway enables Salmonella to balance glucose utilization with aerobic respiratory outputs. Salmonella take advantage of the metabolic flexibility associated with the glutathione-consuming methylglyoxal pathway to resist reactive oxygen species generated by the enzymatic activity of the phagocyte NADPH oxidase in macrophages and mice. Taken together, glutathione fosters oxidative stress resistance in Salmonella against the antimicrobial actions of the phagocyte NADPH oxidase by promoting the methylglyoxal pathway, an offshoot metabolic adaptation of glycolysis. |
Audience | Academic |
Author | Kant, Sashi Vazquez-Torres, Andres Liu, Lin |
AuthorAffiliation | 1 University of Colorado School of Medicine, Department of Immunology and Microbiology, Aurora, Colorado, United States of America University of California Davis School of Medicine, UNITED STATES 2 Veterans Affairs, Eastern Colorado Health Care System, Aurora, Colorado, United States of America |
AuthorAffiliation_xml | – name: 2 Veterans Affairs, Eastern Colorado Health Care System, Aurora, Colorado, United States of America – name: 1 University of Colorado School of Medicine, Department of Immunology and Microbiology, Aurora, Colorado, United States of America – name: University of California Davis School of Medicine, UNITED STATES |
Author_xml | – sequence: 1 givenname: Sashi surname: Kant fullname: Kant, Sashi organization: University of Colorado School of Medicine, Department of Immunology and Microbiology, Aurora, Colorado, United States of America – sequence: 2 givenname: Lin surname: Liu fullname: Liu, Lin organization: University of Colorado School of Medicine, Department of Immunology and Microbiology, Aurora, Colorado, United States of America – sequence: 3 givenname: Andres orcidid: 0000-0002-6181-4185 surname: Vazquez-Torres fullname: Vazquez-Torres, Andres organization: Veterans Affairs, Eastern Colorado Health Care System, Aurora, Colorado, United States of America |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/37267419$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1016_j_chom_2024_01_004 crossref_primary_10_1016_j_plantsci_2023_111922 |
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SubjectTerms | Analysis Animals Antimicrobial agents Biology and Life Sciences Control Cytotoxicity Dextrose Enzymatic activity Genes Glucose Glucose metabolism Glutathione Glutathione - metabolism Glycolysis Health aspects Hydrogen peroxide Hydrogen Peroxide - metabolism Identification and classification Macrophages Medicine and Health Sciences Metabolism Mice Molecular modelling NAD(P)H oxidase NADPH Oxidases - metabolism Oxidase Oxidases Oxidation Oxidation resistance Oxidative Stress Oxygen Peroxides Phagocytes Phosphorylation Physical Sciences Properties Pyruvaldehyde Pyruvaldehyde - metabolism Reactive oxygen species Reactive Oxygen Species - metabolism Respiration Respiratory burst Salmonella Salmonella typhimurium - metabolism Scientific equipment and supplies industry Superoxide Superoxides Toxicity |
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Title | The methylglyoxal pathway is a sink for glutathione in Salmonella experiencing oxidative stress |
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