The Fbe (SdrG) protein of Staphylococcus epidermidis HB promotes bacterial adherence to fibrinogen

O. Hartford, L. O'Brien, K. Schofield, J. Wells, T.J. Foster*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

101 Citations (Scopus)

Abstract

Staphylococcus epidermidis strains HB and K28 express surface proteins called Fbe or SdrG, respectively, that have sequence similarity to the clumping factors ClfA and ClfB of Staphylococcus aureus. A mutation in the fbe gene of strain HB was isolated by directed plasmid integration using the broad-host-range temperature-sensitive plasmid pG+Host9 (pVE6155). An internal fragment of fbe was cloned into pG+Host9 and the chimaeric plasmid was mobilized from S. aureus RN4220 to S. epidermidis 9142 by conjugation promoted by plasmid pGO1. The plasmid was then transferred to S. epidermidis strain HB by phage-48-mediated transduction. The plasmid integrated into the chromosomal fbe gene at a frequency of 2.8 × 10-4. All the survivors tested had a copy of pG+Host9fbe' integrated into the chromosomal fbe gene either as a single copy or as a tandem array. Western immunoblotting showed that the wall-associated Fbe protein was absent in the mutant. Wild-type S. epidermidis HB adhered to immobilized fibrinogen in a dose-dependent and saturable fashion whereas the mutant did not bind. The Fbe proteins of HB and K28 were expressed at a high level in Lactococcus lactis MG1363 using the expression vector pKS80. These strains adhered strongly to immobilized fibrinogen. These results confirm that Fbe is a fibrinogen-binding adhesin.

Original languageEnglish
Pages (from-to)2545-2552
Number of pages8
JournalMicrobiology
Volume147
Issue number9
DOIs
Publication statusPublished - 1 Sep 2001
Externally publishedYes

Keywords

  • Adhesion
  • Lactococcus lactis
  • MSCRAMM
  • Surface protein

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