Your browser doesn't support javascript.
loading
Exogenous Alginate Protects Staphylococcus aureus from Killing by Pseudomonas aeruginosa.
Price, Courtney E; Brown, Dustin G; Limoli, Dominique H; Phelan, Vanessa V; O'Toole, George A.
Affiliation
  • Price CE; Department of Microbiology and Immunology, Geisel School of Medicine at Dartmouth, Hannover, New Hampshire, USA.
  • Brown DG; Department of Pharmaceutical Sciences, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado, Aurora, Colorado, USA.
  • Limoli DH; Department of Microbiology and Immunology, University of Iowa, Iowa City, Iowa, USA.
  • Phelan VV; Department of Pharmaceutical Sciences, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado, Aurora, Colorado, USA.
  • O'Toole GA; Department of Microbiology and Immunology, Geisel School of Medicine at Dartmouth, Hannover, New Hampshire, USA georgeo@dartmouth.edu.
J Bacteriol ; 202(8)2020 03 26.
Article in En | MEDLINE | ID: mdl-31792010
ABSTRACT
Cystic fibrosis (CF) patients chronically infected with both Pseudomonas aeruginosa and Staphylococcus aureus have worse health outcomes than patients who are monoinfected with either P. aeruginosa or S. aureus We showed previously that mucoid strains of P. aeruginosa can coexist with S. aureusin vitro due to the transcriptional downregulation of several toxic exoproducts typically produced by P. aeruginosa, including siderophores, rhamnolipids, and HQNO (2-heptyl-4-hydroxyquinoline N-oxide). Here, we demonstrate that exogenous alginate protects S. aureus from P. aeruginosa in both planktonic and biofilm coculture models under a variety of nutritional conditions. S. aureus protection in the presence of exogenous alginate is due to the transcriptional downregulation of pvdA, a gene required for the production of the iron-scavenging siderophore pyoverdine as well as the downregulation of the PQS (Pseudomonas quinolone signal) (2-heptyl-3,4-dihydroxyquinoline) quorum sensing system. The impact of exogenous alginate is independent of endogenous alginate production. We further demonstrate that coculture of mucoid P. aeruginosa with nonmucoid P. aeruginosa strains can mitigate the killing of S. aureus by the nonmucoid strain of P. aeruginosa, indicating that the mechanism that we describe here may function in vivo in the context of mixed infections. Finally, we investigated a panel of mucoid clinical isolates that retain the ability to kill S. aureus at late time points and show that each strain has a unique expression profile, indicating that mucoid isolates can overcome the S. aureus-protective effects of mucoidy in a strain-specific manner.IMPORTANCE CF patients are chronically infected by polymicrobial communities. The two dominant bacterial pathogens that infect the lungs of CF patients are P. aeruginosa and S. aureus, with ∼30% of patients coinfected by both species. Such coinfected individuals have worse outcomes than monoinfected patients, and both species persist within the same physical space. A variety of host and environmental factors have been demonstrated to promote P. aeruginosa-S. aureus coexistence, despite evidence that P. aeruginosa kills S. aureus when these organisms are cocultured in vitro Thus, a better understanding of P. aeruginosa-S. aureus interactions, particularly mechanisms by which these microorganisms are able to coexist in proximal physical space, will lead to better-informed treatments for chronic polymicrobial infections.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pseudomonas aeruginosa / Pseudomonas Infections / Staphylococcal Infections / Staphylococcus aureus / Cystic Fibrosis / Alginates Type of study: Prognostic_studies Limits: Humans Language: En Journal: J Bacteriol Year: 2020 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pseudomonas aeruginosa / Pseudomonas Infections / Staphylococcal Infections / Staphylococcus aureus / Cystic Fibrosis / Alginates Type of study: Prognostic_studies Limits: Humans Language: En Journal: J Bacteriol Year: 2020 Document type: Article Affiliation country: United States
...