VISLISI trial, a prospective clinical study allowing identification of a new metalloprotease and putative virulence factor from Staphylococcus lugdunensis

Clin Microbiol Infect. 2017 May;23(5):334.e1-334.e8. doi: 10.1016/j.cmi.2016.12.018. Epub 2016 Dec 23.

Abstract

Objective: Staphylococcus lugdunensis is a coagulase-negative staphylococcus that displays an unusually high virulence rate close to that of Staphylococcus aureus. It also shares phenotypic properties with S. aureus and several studies found putative virulence factors. The objective of the study was to describe the clinical manifestations of S. lugdunensis infections and investigate putative virulence factors.

Method: We conducted a prospective study from November 2013 to March 2016 at the University Hospital of Strasbourg. Putative virulence factors were investigated by clumping factor detection, screening for proteolytic activity, and sequence analysis using tandem nano-liquid chromatography-mass spectrometry.

Results: In total, 347 positive samples for S. lugdunensis were collected, of which 129 (37.2%) were from confirmed cases of S. lugdunensis infection. Eighty-one of these 129 patients were included in the study. Bone and prosthetic joints (PJI) were the most frequent sites of infection (n=28; 34.6%) followed by skin and soft tissues (n=23; 28.4%). We identified and purified a novel protease secreted by 50 samples (61.7%), most frequently associated with samples from deep infections and PJI (pr 0.97 and pr 0.91, respectively). Protease peptide sequencing by nano-liquid chromatography-mass spectrometry revealed a novel protease bearing 62.42% identity with ShpI, a metalloprotease secreted by Staphylococcus hyicus.

Conclusion: This study confirms the pathogenicity of S. lugdunensis, particularly in bone and PJI. We also identified a novel metalloprotease called lugdulysin that may contribute to virulence.

Keywords: Bone and joint infections; Mass spectrometry; Metalloprotease; Staphylococcus lugdunensis; Virulence factors.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Amino Acid Sequence
  • Aminoglycosides / therapeutic use
  • Base Sequence
  • DNA, Bacterial / genetics
  • Drug Resistance, Multiple, Bacterial
  • Erythromycin / therapeutic use
  • Female
  • Fluoroquinolones / therapeutic use
  • Follow-Up Studies
  • Fosfomycin / therapeutic use
  • Fusidic Acid / therapeutic use
  • Humans
  • Male
  • Metalloproteases / genetics*
  • Metalloproteases / metabolism
  • Methicillin / therapeutic use
  • Middle Aged
  • Phosphonoacetic Acid / therapeutic use
  • Prospective Studies
  • Sequence Analysis, DNA
  • Staphylococcal Infections / diagnosis
  • Staphylococcal Infections / drug therapy
  • Staphylococcus lugdunensis / enzymology*
  • Staphylococcus lugdunensis / genetics
  • Staphylococcus lugdunensis / pathogenicity
  • Vancomycin / therapeutic use
  • Virulence Factors / genetics*

Substances

  • Aminoglycosides
  • DNA, Bacterial
  • Fluoroquinolones
  • Virulence Factors
  • Fosfomycin
  • Fusidic Acid
  • Erythromycin
  • Vancomycin
  • Metalloproteases
  • Phosphonoacetic Acid
  • Methicillin