4.2 Article

Effect of incubation atmosphere on the production and composition of staphylococcal biofilms

Journal

JOURNAL OF INFECTION AND CHEMOTHERAPY
Volume 21, Issue 1-2, Pages 55-61

Publisher

ELSEVIER
DOI: 10.1016/j.jiac.2014.10.001

Keywords

Biofilm composition; Staphylococcus aureus; Staphylococcus epidermidis; Poly-beta (1,6)-N-acetyl-D-glucosamine; Extracellular DNA; Microbial surface components recognizing adhesive matrix molecules

Funding

  1. MEXT/JSPS KAKENHI, Japan [20790332, 24790551]
  2. Grants-in-Aid for Scientific Research [24790551] Funding Source: KAKEN

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Staphylococcus aureus and Staphylococcus epidermidis are pathogenic bacteria that often cause invasive infections in humans. In this study, we characterized the composition and growth characteristics of staphylococcal biofilms under various incubation atmospheres. We assessed the effect of incubation atmosphere (aerobic, 5% CO2, anaerobic, and microaerobic) on the biofilm production capabilities of S. aureus strains isolated from healthy volunteers and from patients with catheter-related bloodstream infection. In addition, the composition of S. aureus and S. epidermidis biofilms was determined by assessment of biofilm degradation after treatment with DNase I, proteinase K, and dispersin B. The strains obtained from healthy volunteers and patients showed similar biofilm formation capabilities. Biofilms of S. aureus were rich in proteins when developed under ambient atmospheric conditions, 5% CO2, and microaerobic condition, whereas S. epidermidis biofilms contained large amounts of poly-beta (1, 6)-N-acetyl-D-glucosamine when developed under ambient atmospheric conditions and microaerobic condition. The biofilm-producing capability of S. epidermidis was considerably higher than that of S. aureus under aerobic condition. Staphylococcal isolates obtained from healthy individuals and patients with catheter-related infections have similar biofilm-forming capabilities. Under microaerobic conditions, S. aureus and S. epidermidis form protein-rich and poly-beta (1, 6)-N-acetyl-D-glucosamine-rich biofilms, respectively. These components may play an important role in the development of biofilms inside the body and may be the target molecules to prevent catheter-related infections caused by these organisms. (C) 2014, Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases. Published by Elsevier Ltd. All rights reserved.

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