» Articles » PMID: 31040245

Protease-Mediated Growth of Staphylococcus Aureus on Host Proteins Is Dependent

Overview
Journal mBio
Specialty Microbiology
Date 2019 May 2
PMID 31040245
Citations 26
Authors
Affiliations
Soon will be listed here.
Abstract

has the ability to cause infections in multiple organ systems, suggesting an ability to rapidly adapt to changing carbon and nitrogen sources. Although there is little information about the nutrients available at specific sites of infection, a mature skin abscess has been characterized as glucose depleted, indicating that peptides and free amino acids are an important source of nutrients for the bacteria. Our studies have found that mutations in enzymes necessary for growth on amino acids, including pyruvate carboxykinase (Δ) and glutamate dehydrogenase (Δ), reduced the ability of the bacteria to proliferate within a skin abscess, suggesting that peptides and free amino acids are important for growth. Furthermore, we found that collagen, an abundant host protein that is present throughout a skin abscess, serves as a reservoir of peptides. To liberate peptides from the collagen, we identified that the host protease, MMP-9, as well as the staphylococcal proteases aureolysin and staphopain B function to cleave collagen into peptide fragments that can support growth under nutrient-limited conditions. Moreover, the oligopeptide transporter Opp3 is the primary staphylococcal transporter responsible for peptide acquisition. Lastly, we observed that the presence of peptides (3-mer to 7-mer) induces the expression of aureolysin, suggesting that has the ability to detect peptides in the environment. has the ability to cause infections in a variety of niches, suggesting a robust metabolic capacity facilitating proliferation under various nutrient conditions. The mature skin abscess is glucose depleted, indicating that peptides and free amino acids are important sources of nutrients for Our studies have found that mutations in both pyruvate carboxykinase and glutamate dehydrogenase, enzymes that function in essential gluconeogenesis reactions when amino acids serve as the major carbon source, reduce bacterial burden in a murine skin abscess model. Moreover, peptides liberated from collagen by host protease MMP-9 as well as the staphylococcal protease aureolysin support growth in an Opp3-dependent manner under nutrient-limited conditions. Additionally, the presence of peptides induces aureolysin expression. Overall, these studies define one pathway by which senses a nutrient-limiting environment and induces factors that function to acquire and utilize carbon from host-derived sources.

Citing Articles

Proteins Implicated in the Reduced Virulence of and Mutants in Osteomyelitis.

Beenken K, Campbell M, Byrum S, Edmondson R, Mackintosh S, Tackett A Microorganisms. 2025; 13(1).

PMID: 39858949 PMC: 11767506. DOI: 10.3390/microorganisms13010181.


Regulatory dynamics of arginine metabolism in Staphylococcus aureus.

Reslane I, Watson G, Handke L, Fey P Biochem Soc Trans. 2024; 52(6):2513-2523.

PMID: 39656074 PMC: 11668279. DOI: 10.1042/BST20240710.


The ability of to limit protease production plays a key role in the pathogenesis of osteomyelitis irrespective of the functional status of .

Beenken K, Campbell M, Smeltzer M Infect Immun. 2024; 93(1):e0047324.

PMID: 39611695 PMC: 11784413. DOI: 10.1128/iai.00473-24.


Aging-Induced Changes in and Their Effects on Skin Elasticity and Wrinkle Formation.

Jung Y, Kim I, Jung D, Ha J, Lee E, Kim J Microorganisms. 2024; 12(11).

PMID: 39597568 PMC: 11596587. DOI: 10.3390/microorganisms12112179.


Metabolites augment oxidative stress to sensitize antibiotic-tolerant to fluoroquinolones.

Batchelder J, Taylor A, Mok W mBio. 2024; 15(12):e0271424.

PMID: 39475229 PMC: 11633220. DOI: 10.1128/mbio.02714-24.


References
1.
De Bentzmann S, Polette M, Zahm J, Hinnrasky J, Kileztky C, Bajolet O . Pseudomonas aeruginosa virulence factors delay airway epithelial wound repair by altering the actin cytoskeleton and inducing overactivation of epithelial matrix metalloproteinase-2. Lab Invest. 2000; 80(2):209-19. DOI: 10.1038/labinvest.3780024. View

2.
Stevanin T, Ioannidis N, Mills C, Kim S, Hughes M, Poole R . Flavohemoglobin Hmp affords inducible protection for Escherichia coli respiration, catalyzed by cytochromes bo' or bd, from nitric oxide. J Biol Chem. 2000; 275(46):35868-75. DOI: 10.1074/jbc.M002471200. View

3.
Rice K, Peralta R, Bast D, de Azavedo J, McGavin M . Description of staphylococcus serine protease (ssp) operon in Staphylococcus aureus and nonpolar inactivation of sspA-encoded serine protease. Infect Immun. 2000; 69(1):159-69. PMC: 97868. DOI: 10.1128/IAI.69.1.159-169.2001. View

4.
McAleese F, Walsh E, Sieprawska M, Potempa J, Foster T . Loss of clumping factor B fibrinogen binding activity by Staphylococcus aureus involves cessation of transcription, shedding and cleavage by metalloprotease. J Biol Chem. 2001; 276(32):29969-78. DOI: 10.1074/jbc.M102389200. View

5.
Karlsson A, Tegmark K, Morfeldt E, Arvidson S . Decreased amounts of cell wall-associated protein A and fibronectin-binding proteins in Staphylococcus aureus sarA mutants due to up-regulation of extracellular proteases. Infect Immun. 2001; 69(8):4742-8. PMC: 98560. DOI: 10.1128/IAI.69.8.4742-4748.2001. View