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 inPLoS pathogens Vol. 19; no. 6; p. e1011441
Main Authors Kant, Sashi, Liu, Lin, Vazquez-Torres, Andres
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 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.
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
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– name: University of California Davis School of Medicine, UNITED STATES
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Snippet Salmonella suffer the cytotoxicity of reactive oxygen species generated by the phagocyte NADPH oxidase in the innate host response. Periplasmic superoxide...
Salmonella suffer the cytotoxicity of reactive oxygen species generated by the phagocyte NADPH oxidase in the innate host response. Periplasmic superoxide...
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StartPage e1011441
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
URI https://www.ncbi.nlm.nih.gov/pubmed/37267419
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https://pubmed.ncbi.nlm.nih.gov/PMC10266609
https://doaj.org/article/f6fe1959929c4811b6b648aae8e04986
http://dx.doi.org/10.1371/journal.ppat.1011441
Volume 19
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