Increased in vitro phenol-soluble modulin production is associated with soft tissue infection source in clinical isolates of methicillin-susceptible Staphylococcus aureus

dc.contributor.authorQi, Robert
dc.contributor.authorJoo, Hwang-Soo
dc.contributor.authorSharma-Kuinkel, Batu K.
dc.contributor.authorBerlon, Nicholas R.
dc.contributor.authorPark, Lawrence P.
dc.contributor.authorFu, Chihlung
dc.contributor.authorMessina, Julia A.
dc.contributor.authorThaden, Joshua T.
dc.contributor.authorYan, Qin
dc.contributor.authorRuffin, Felicia
dc.contributor.authorMaskarinec, Stacey A.
dc.contributor.authorWarren, Bobby Glenn
dc.contributor.authorChu, Vivian H.
dc.contributor.authorFortes, Claudio Querido
dc.contributor.authorGiannitsioti, Efthymia
dc.contributor.authorDurante-Mangoni, Emanuele
dc.contributor.authorKanafani, Zeina A.
dc.contributor.authorOtto, Michael
dc.contributor.authorFowler, Vance G.
dc.contributor.departmentInternal Medicine
dc.contributor.departmentDivision of Infectious Diseases
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:48:39Z
dc.date.available2025-01-24T11:48:39Z
dc.date.issued2016
dc.description.abstractBackground: Phenol-soluble modulins (PSM) are amphipathic proteins produced by Staphylococcus aureus that promote virulence, inflammatory response, and biofilm formation. We previously showed that MRSA isolates from soft tissue infection (SSTI) produced significantly higher levels of PSM than MRSA isolates from hospital-acquired pneumonia (HAP) or infective endocarditis (IE). In this investigation, we sought to validate this finding in methicillin-susceptible S. aureus (MSSA) isolates. Methods: MSSA isolates (n = 162) from patients with SSTI, HAP, and IE were matched 1:1:1 based on geographic origin of the infection to form 54 triplets (North America n = 27, Europe n = 25, Australia n = 2). All isolates underwent spa typing and were classified using eGenomics. In vitro PSM production was quantified by high-performance liquid chromatography/mass spectrometry. Fischer's Exact Test and the Kruskal-Wallis test were used for statistical analysis. Results: Spa1 was more common in SSTI (14.81% SSTI, 3.70% HAP, 1.85% IE) (< 0.03). Spa2 was more common in HAP (0% SSTI, 12.96% HAP, 3.70% IE) (< 0.01). Levels of PSMα1-all differed significantly among the three clinical groups, with SSTI isolates producing the highest levels and IE producing the lowest levels of PSMα1-4. Spa1 isolates produced significantly more delta-toxin (< 0.03) than non-Spa1 isolates. No associations between PSM levels and clinical outcome of SSTI, HAP, or IE were identified. Conclusion: Production of PSMα1-is highest in SSTI MSSA isolates, supporting the hypothesis that these peptides are important for SSTI pathogenesis. These findings are similar to those described in MRSA, and demonstrate that associations between PSM levels and type of infection are independent of the methicillin-resistance status of the isolate. © 2015 The British Infection Association.
dc.identifier.doihttps://doi.org/10.1016/j.jinf.2015.11.002
dc.identifier.eid2-s2.0-84958180375
dc.identifier.pmid26778460
dc.identifier.urihttp://hdl.handle.net/10938/30832
dc.language.isoen
dc.publisherW.B. Saunders Ltd
dc.relation.ispartofJournal of Infection
dc.sourceScopus
dc.subjectEndocarditis
dc.subjectMethicillin-susceptible staphylococcus aureus
dc.subjectPhenol-soluble modulin
dc.subjectPneumonia
dc.subjectSkin and soft tissue infection
dc.subjectAdolescent
dc.subjectAdult
dc.subjectAged
dc.subjectAged, 80 and over
dc.subjectAustralia
dc.subjectBacterial toxins
dc.subjectChromatography, high pressure liquid
dc.subjectEurope
dc.subjectFemale
dc.subjectHumans
dc.subjectMale
dc.subjectMass spectrometry
dc.subjectMiddle aged
dc.subjectMolecular typing
dc.subjectNorth america
dc.subjectSoft tissue infections
dc.subjectStaphylococcal infections
dc.subjectStaphylococcal protein a
dc.subjectStaphylococcus aureus
dc.subjectYoung adult
dc.subjectBacterial protein
dc.subjectPhenol soluble modulin
dc.subjectPhenol soluble modulin alpha1
dc.subjectPhenol soluble modulin alpha2
dc.subjectPhenol soluble modulin alpha3
dc.subjectPhenol soluble modulin alpha4
dc.subjectUnclassified drug
dc.subjectBacterial toxin
dc.subjectStaphylococcal delta toxin
dc.subjectStaphylococcus protein a
dc.subjectArticle
dc.subjectBacterial endocarditis
dc.subjectBacterium identification
dc.subjectBacterium isolation
dc.subjectDisease association
dc.subjectGeographic origin
dc.subjectHigh performance liquid chromatography
dc.subjectHospital acquired pneumonia
dc.subjectHuman
dc.subjectIn vitro study
dc.subjectMethicillin susceptible staphylococcus aureus
dc.subjectNonhuman
dc.subjectPathogenesis
dc.subjectProtein synthesis
dc.subjectQuantitative analysis
dc.subjectSoft tissue infection
dc.subjectStaphylococcus infection
dc.subjectClassification
dc.subjectGenetics
dc.subjectIsolation and purification
dc.subjectMetabolism
dc.subjectMicrobiology
dc.subjectVery elderly
dc.titleIncreased in vitro phenol-soluble modulin production is associated with soft tissue infection source in clinical isolates of methicillin-susceptible Staphylococcus aureus
dc.typeArticle

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