Staphylococcus aureus (S. aureus) is a leading cause of human infections worldwide, resulting in a diverse spectrum of disease severity from mild to life-threatening. Recently, there has been an increase in the incidence of community-associated methicillin-resistant S. aureus (CA-MRSA) infections in otherwise healthy individuals, the basis of which is largely unknown. Human polymorphonuclear leukocytes (PMNs or neutrophils) are the first line of defense against bacterial infections. The ability of S. aureus to circumvent destruction by innate immunity includes survival after PMN phagocytosis. The ability of S. aureus to survive following PMN phagocytosis is dependent on the pathogen's ability to sense and survive the hostile PMN environment. However, specific mechanisms used by S. aureus to evade PMN killing are incompletely defined. We hypothesize that the SaeR/S two-component regulatory system directly regulates S. aureus factors that impair an effective neutrophil response resulting in pathogen survival. This hypothesis is based on the following published and preliminary observations: 1) saeR and saeS transcripts were up-regulated following PMN phagocytosis;2) deletion of saeR/S significantly decreased survival of S. aureus following human PMN phagocytosis;and 3) transcriptional assays identified extracellular virulence genes down- regulated in saeR/S and direct binding of recombinant SaeR to a consensus sequence within several of these virulence gene promoters. These data correlate well with in vivo studies that demonstrate SaeR/S regulates factors vital for S. aureus - induced morbidity following skin infections and mortality following invasive infections. To determine the molecular mechanisms behind the saeR/S-dependent phenotype we will first define the kinetics of activation of SaeR/S-regulated genes in response to PMN phagocytosis. Next, we will determine the contribution of individual SaeR/S-target genes to S. aureus survival and PMN lysis. Finally, we will assess expression of saeR/S-target genes in vivo and identify the contribution of individual genes regulated by saeR/S to S. aureus pathogenesis. Completion of this research will identify the specific effectors regulated by saeR/S responsible for survival following PMN phagocytosis and will define their contribution to PMN lysis and S. aureus pathogenesis in vivo. These findings will improve our understanding of the initial host-pathogen interactions that lead to S. aureus infection. This knowledge is predicted to have direct application for novel prevention and treatment strategies for staphylococcal infections.

Public Health Relevance

Staphylcoccus aureus (S. aureus) is a leading cause of morbidity and mortality worldwide. The emergence of hyper-infectious community-associated methicillin resistant (CA-MRSA) strains within the community is a major public health concern. Given the diminishing effectiveness of our current antibiotics, it is clear we must improve our understanding of molecular mechanisms fundamental to S. aureus pathogenesis in order to develop better methods to control/treat S. aureus disease and thus improve public health.

Agency
National Institute of Health (NIH)
Type
Research Project (R01)
Project #
5R01AI090046-04
Application #
8690746
Study Section
Host Interactions with Bacterial Pathogens Study Section (HIBP)
Program Officer
Huntley, Clayton C
Project Start
Project End
Budget Start
Budget End
Support Year
4
Fiscal Year
2014
Total Cost
Indirect Cost
Name
Montana State University - Bozeman
Department
Veterinary Sciences
Type
Earth Sciences/Resources
DUNS #
City
Bozeman
State
MT
Country
United States
Zip Code
59717
Olson, Michael E; Nygaard, Tyler K; Ackermann, Laynez et al. (2013) Staphylococcus aureus nuclease is an SaeRS-dependent virulence factor. Infect Immun 81:1316-24
Watkins, Robert L; Zurek, Oliwia W; Pallister, Kyler B et al. (2013) The SaeR/S two-component system induces interferon-gamma production in neutrophils during invasive Staphylococcus aureus infection. Microbes Infect 15:749-54
Nygaard, Tyler K; Pallister, Kyler B; Zurek, Oliwia W et al. (2013) The impact of *-toxin on host cell plasma membrane permeability and cytokine expression during human blood infection by CA-MRSA USA300. J Leukoc Biol 94:971-9