Versatility of Biofilm Matrix Molecules in Staphylococcus epidermidis Clinical Isolates and Importance of Polysaccharide Intercellular Adhesin Expression during High Shear Stress

Author:

Schaeffer Carolyn R.1,Hoang Tra-My N.1,Sudbeck Craig M.1,Alawi Malik2,Tolo Isaiah E.3,Robinson D. Ashley3,Horswill Alexander R.4,Rohde Holger5,Fey Paul D.1

Affiliation:

1. Department of Pathology and Microbiology, Center for Staphylococcal Research, University of Nebraska Medical Center, Omaha, Nebraska, USA

2. Bioinformatics Service Facility, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany

3. Department of Microbiology and Immunology, University of Mississippi Medical Center, Jackson, Mississippi, USA

4. Department of Microbiology, University of Iowa, Iowa City, Iowa, USA

5. Institut für Medizinische Mikrobiologie, Virologie und Hygiene, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany

Abstract

Staphylococcus epidermidis is a leading cause of infections related to biomaterials, mostly due to their ability to form biofilm. Biofilm accumulation mechanisms vary, including those that are dependent on specific proteins, environmental DNA (eDNA), or polysaccharide intercellular adhesin (PIA). We found that those isolates obtained from high-shear environments, such as the lumen of a catheter, are more likely to produce PIA-mediated biofilms than those isolates obtained from a low-shear biomaterial-related infection. This suggests that PIA functions as a mechanism that is protective against shear flow. Finally, we performed selection experiments documenting the heterogeneity of biofilm accumulation molecules that function in the absence of PIA, further documenting the biofilm-forming potential of S. epidermidis .

Funder

HHS | NIH | National Institute of Allergy and Infectious Diseases

HHS | NIH | National Institute of General Medical Sciences

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

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