Staphylococcus aureus Responds to the Central Metabolite Pyruvate To Regulate Virulence

Author:

Harper Lamia1,Balasubramanian Divya1,Ohneck Elizabeth A.1,Sause William E.1,Chapman Jessica2,Mejia-Sosa Bryan3,Lhakhang Tenzin4,Heguy Adriana5,Tsirigos Aristotelis4,Ueberheide Beatrix2,Boyd Jeffrey M.6ORCID,Lun Desmond S.3,Torres Victor J.1

Affiliation:

1. Department of Microbiology, New York University School of Medicine, Alexandria Center for Life Science, New York, New York, USA

2. Proteomics Resource Center, Office of Collaborative Science, NYU School of Medicine, New York, New York, USA

3. Center for Computational and Integrative Biology and Department of Computer Science, Rutgers University, Camden, New Jersey, USA

4. Applied Bioinformatics Center, Office of Collaborative Science, NYU School of Medicine, New York, New York, USA

5. Genome Technology Center, Office of Collaborative Science, NYU School of Medicine, New York, New York, USA

6. Department of Biochemistry and Microbiology, Rutgers University, New Brunswick, New Jersey, USA

Abstract

ABSTRACT Staphylococcus aureus is a versatile bacterial pathogen that can cause significant disease burden and mortality. Like other pathogens, S. aureus must adapt to its environment to produce virulence factors to survive the immune responses evoked by infection. Despite the importance of environmental signals for S. aureus pathogenicity, only a limited number of these signals have been investigated in detail for their ability to modulate virulence. Here we show that pyruvate, a central metabolite, causes alterations in the overall metabolic flux of S. aureus and enhances its pathogenicity. We demonstrate that pyruvate induces the production of virulence factors such as the pore-forming leucocidins and that this induction results in increased virulence of community-acquired methicillin-resistant S. aureus (CA-MRSA) clone USA300. Specifically, we show that an efficient “pyruvate response” requires the activation of S. aureus master regulators AgrAC and SaeRS as well as the ArlRS two-component system. Altogether, our report further establishes a strong relationship between metabolism and virulence and identifies pyruvate as a novel regulatory signal for the coordination of the S. aureus virulon through intricate regulatory networks. IMPORTANCE Delineation of the influence of host-derived small molecules on the makeup of human pathogens is a growing field in understanding host-pathogen interactions. S. aureus is a prominent pathogen that colonizes up to one-third of the human population and can cause serious infections that result in mortality in ~15% of cases. Here, we show that pyruvate, a key nutrient and central metabolite, causes global changes to the metabolic flux of S. aureus and activates regulatory networks that allow significant increases in the production of leucocidins. These and other virulence factors are critical for S. aureus to infect diverse host niches, initiate infections, and effectively subvert host immune responses. Understanding how environmental signals, particularly ones that are essential to and prominent in the human host, affect virulence will allow us to better understand pathogenicity and consider more-targeted approaches to tackling the current S. aureus epidemic.

Funder

HHS | NIH | National Cancer Institute

HHS | NIH | National Institute of Allergy and Infectious Diseases

National Science Foundation

HHS | NIH | National Center for Advancing Translational Sciences

United Negro College Fund Special Programs Corporation

Publisher

American Society for Microbiology

Subject

Virology,Microbiology

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