Staphylococcus aureus is a major human pathogen of the respiratory tract and influenza co-infection is a major predisposing factor for subsequent infection. Colonization of the upper respiratory tract is also a significant factor in infection, with aspirated organisms reaching the lung and leading to host immunopathology. The host processes involved in S. aureus colonization and subsequent dissemination to the lung are not well understood, but we have identified two pathways that are activated upon S. aureus infection, the type I and type III IFN pathways. Type I and III IFN signaling contribute to the ability of S. aureus to colonize the nasopharynx during influenza co-infection as well as during acute pneumonia where they contribute to excessive immunopathology.
In Aim 1 we will investigate mechanisms behind IFNs increasing susceptibility to S. aureus colonization during influenza co-infection.
This aim will utilize an in vivo co-infection model of colonization examining: IFNs changing the cytokine response, antimicrobial peptide changes of the microbiome and the role of sialic acid and influenza neuraminidase in biofilm formation and colonization.
In Aim 2 we will examine the consequences of respiratory epithelial IFN activation to S. aureus, examining changes in cytokines and their influence of macrophages and neutrophil function. We will also examine the utility of IFN antibody neutralization in clearing infection and in concert with current antimicrobials. At the conclusion of these studies, we will have expanded our knowledge on how IFNs contribute to the pathogenesis of S. aureus colonization and pneumonia, and will have identified targetable mechanisms for therapeutic amelioration of host immunopathology due to IFN production.
Staphylococcus aureus is a common pathogen that leads to a broad range of infections, including pneumonia. Prior to infection many people are colonized in the nose with S. aureus and one pre-disposing factor to infection is co-infection with influenza. This project investigates the mechanisms behind how the type I and III interferon pathways are involved in colonization of the nose and subsequent pneumonia with S. aureus, with the potential of targeting some of these mechanisms for therapeutic intervention.
| Pires, Silvia; Jacquet, Rudy; Parker, Dane (2018) Inducible Costimulator Contributes to Methicillin-Resistant Staphylococcus aureus Pneumonia. J Infect Dis 218:659-668 |
| Parker, Dane (2018) CD80/CD86 signaling contributes to the proinflammatory response of Staphylococcus aureus in the airway. Cytokine 107:130-136 |
| Parker, Dane (2018) A live vaccine to Staphylococcus aureus infection. Virulence 9:700-702 |
| Hook, Jaime L; Islam, Mohammad N; Parker, Dane et al. (2018) Disruption of staphylococcal aggregation protects against lethal lung injury. J Clin Invest 128:1074-1086 |
| Parker, Dane; Prince, Alice (2016) Immunoregulatory effects of necroptosis in bacterial infections. Cytokine 88:274-275 |
| Cohen, Taylor S; Parker, Dane (2016) Microbial pathogenesis and type III interferons. Cytokine Growth Factor Rev 29:45-51 |
