Review

International Journal of Oral Science (2011) 3, 55–65; doi:10.4248/IJOS11026

The clinical impact of bacterial biofilms

Niels Høiby1,2, Oana Ciofu2, Helle Krogh Johansen1, Zhijun Song1, Claus Moser1, Peter Østrup Jensen1, Søren Molin3, Michael Givskov2, Tim TolkerNielsen2 and Thomas Bjarnsholt1,2

  1. 1Department of Clinical Microbiology, Rigshospitalet
  2. 2Institute for International Health, Medical Microbiology and Immunology
  3. 3BioScience and Technology, Biocentrum, Danish Technical University

Correspondence: Niels Høiby, Fax: 45 35456412 E-mail: hoiby@hoibyniels.dk

Received 14 February 2011; Accepted 9 March 2011

Top

Abstract

Bacteria survive in nature by forming biofilms on surfaces and probably most, if not all, bacteria (and fungi) are capable of forming biofilms. A biofilm is a structured consortium of bacteria embedded in a selfproduced polymer matrix consisting of polysaccharide, protein and extracellular DNA. Bacterial biofilms are resistant to antibiotics, disinfectant chemicals and to phagocytosis and other components of the innate and adaptive inflammatory defense system of the body. It is known, for example, that persistence of staphylococcal infections related to foreign bodies is due to biofilm formation. Likewise, chronic Pseudomonas aeruginosa lung infections in cystic fibrosis patients are caused by biofilm growing mucoid strains. Gradients of nutrients and oxygen exist from the top to the bottom of biofilms and the bacterial cells located in nutrient poor areas have decreased metabolic activity and increased doubling times. These more or less dormant cells are therefore responsible for some of the tolerance to antibiotics. Biofilm growth is associated with an increased level of mutations. Bacteria in biofilms communicate by means of molecules, which activates certain genes responsible for production of virulence factors and, to some extent, biofilm structure. This phenomenon is called quorum sensing and depends upon the concentration of the quorum sensing molecules in a certain niche, which depends on the number of the bacteria. Biofilms can be prevented by antibiotic prophylaxis or early aggressive antibiotic therapy and they can be treated by chronic suppressive antibiotic therapy. Promising strategies may include the use of compounds which can dissolve the biofilm matrix and quorum sensing inhibitors, which increases biofilm susceptibility to antibiotics and phagocytosis.

Keywords:

bacterial biofilm; biofilm infection; antibiotic resistance; quorum sensing