Staphylococcus aureus CcpA Affects Biofilm Formation

Seidl, Kati; Goerke, Christiane; Wolz, Christiane; Mack, Dietrich; Berger-Bächi, Brigitte; Bischoff, Markus

doi:10.1128/iai.00035-08

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Journal article

Staphylococcus aureus CcpA Affects Biofilm Formation

Seidl, Kati Institute of Medical Microbiology, University of Zürich, Zürich, Switzerland
Goerke, Christiane Institute for Medical Microbiology and Hygiene, University Hospital—Tübingen, Tübingen, Germany
Wolz, Christiane Institute for Medical Microbiology and Hygiene, University Hospital—Tübingen, Tübingen, Germany
Mack, Dietrich University of Wales—Swansea, Swansea, United Kingdom
Berger-Bächi, Brigitte Institute of Medical Microbiology, University of Zürich, Zürich, Switzerland
Bischoff, Markus Institute of Medical Microbiology and Hygiene, University of Saarland Hospital, Homburg/Saar, Germany

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Infection and Immunity. - American Society for Microbiology. - 2008, vol. 76, no. 5, p. 2044-2050

English ABSTRACT
Biofilm formation in Staphylococcus aureus under in vitro growth conditions is generally promoted by high concentrations of sugar and/or salts. The addition of glucose to routinely used complex growth media triggered biofilm formation in S. aureus strain SA113. Deletion of ccpA, coding for the catabolite control protein A (CcpA), which regulates gene expression in response to the carbon source, abolished the capacity of SA113 to form a biofilm under static and flow conditions, while still allowing primary attachment to polystyrene surfaces. This suggested that CcpA mainly affects biofilm accumulation and intercellular aggregation. trans-Complementation of the mutant with the wild-type ccpA allele fully restored the biofilm formation. The biofilm produced by SA113 was susceptible to sodium metaperiodate, DNase I, and proteinase K treatment, indicating the presence of polysaccharide intercellular adhesin (PIA), protein factors, and extracellular DNA (eDNA). The investigation of several factors which were reported to influence biofilm formation in S. aureus (arlRS, mgrA, rbf, sarA, atl, ica, citZ, citB, and cidABC) showed that CcpA up-regulated the transcription of cidA, which was recently shown to contribute to eDNA production. Moreover, we showed that CcpA increased icaA expression and PIA production, presumably over the down-regulation of the tricarboxylic acid cycle genes citB and citZ.

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