Metabolic control of virulence factor production in Staphylococcus aureus
- PMID: 32388086
- PMCID: PMC7311248
- DOI: 10.1016/j.mib.2020.03.004
Metabolic control of virulence factor production in Staphylococcus aureus
Abstract
As investigators decipher the underlining mechanisms of Staphylococcus aureus pathogenesis, it is becoming apparent that perturbations in central metabolism alter virulence factor production and infection outcomes. It is also evident that S. aureus has the ability to metabolically adapt to improve colonization and overcome challenges imparted by the immune system. Altered metabolite pools modify virulence factor production suggesting that proper functioning of a core metabolic network is necessary for successful niche colonization and pathogenesis. Herein we discuss four examples of transcriptional regulators that monitor metabolic status. These regulatory systems sense perturbations in the metabolic network and respond by altering the transcription of genes utilized for central metabolism, energy generation and pathogenesis.
Copyright © 2020 Elsevier Ltd. All rights reserved.
Conflict of interest statement
Declaration of interests
The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
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References
-
-
Grosser MR, Paluscio E, Thurlow LR, Dillon MM, Cooper VS, Kawula TH, Richardson AR: Genetic requirements for Staphylococcus aureus nitric oxide resistance and virulence. PLoS Pathog 2018, 14:e1006907.
A study using transposon sequencing to determine genes necessary for pathogenesis and nitric oxide resistance. Also contains a comprehensive analysis of potential essential genes.
-
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