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Updated: Dec 9, 2025

A Tandem Liquid Chromatography–Mass Spectrometry-based Approach for Metabolite Analysis of Staphylococcus aureus
Published on: March 28, 2017
Consequences of Metabolic Interactions during Staphylococcus aureus Infection
Alice Prince1, Tania Wong Fok Lung1
1Department of Pediatrics, Vagelos College of Physicians & Surgeons, Columbia University, New York, NY 10032, USA.
Abstract:
Staphylococcus aureus is a metabolically flexible pathogen that causes infection in diverse settings. An array of virulence factors, including the secreted toxins, enables S. aureus to colonize different environmental niches and initiate infections by any of several discrete pathways. During these infections, both S. aureus and host cells compete with each other for nutrients and remodel their metabolism for survival. This metabolic interaction/crosstalk determines the outcome of the infection. The reprogramming of metabolic pathways in host immune cells not only generates adenosine triphosphate (ATP) to meet the cellular energy requirements during the infection process but also activates antimicrobial responses for eventual bacterial clearance, including cell death pathways. The selective pressure exerted by host immune cells leads to the emergence of bacterial mutants adapted for chronicity. These host-adapted mutants are often characterized by substantial changes in the expression of their own metabolic genes, or by mutations in genes involved in metabolism and biofilm formation. Host-adapted S. aureus can rewire or benefit from the metabolic activities of the immune cells via several mechanisms to cause persistent infection. In this review, we discuss how S. aureus activates host innate immune signaling, which results in an immune metabolic pressure that shapes S. aureus metabolic adaptation and determines the outcome of the infection.
Insights
Staphylococcus aureus adapts its metabolism to survive host immune responses during infection. This metabolic crosstalk influences infection outcomes and can lead to chronic Staphylococcus aureus infections.
Area of Science:
- Microbiology
- Immunology
- Metabolic pathways
Background:
- Staphylococcus aureus is a versatile pathogen causing diverse infections.
- Virulence factors and secreted toxins enable S. aureus colonization and infection initiation.
- Host-pathogen metabolic competition and adaptation are crucial during infection.
Purpose of the Study:
- To review the metabolic interactions between Staphylococcus aureus and host immune cells.
- To elucidate how immune metabolic pressure shapes S. aureus adaptation.
- To understand the role of metabolic crosstalk in determining infection outcomes.
Main Methods:
- Literature review of studies on Staphylococcus aureus metabolism and host immune responses.
- Analysis of metabolic reprogramming in host immune cells during infection.
- Examination of bacterial adaptation mechanisms and gene expression changes.
Main Results:
- Host immune cell metabolic reprogramming generates ATP and activates antimicrobial responses.
- S. aureus and host cells compete for nutrients, driving metabolic adaptation.
- Host-selective pressures promote the emergence of chronicity-adapted S. aureus mutants with altered metabolism and biofilm formation.
- Host-adapted S. aureus utilizes host immune cell metabolic activities for persistent infections.
Conclusions:
- Metabolic crosstalk between S. aureus and host immune cells is a key determinant of infection outcome.
- S. aureus activates host innate immune signaling, leading to metabolic pressure that drives bacterial adaptation.
- Understanding these metabolic interactions is vital for developing strategies against persistent S. aureus infections.
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