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Antimicrobial Agents and Chemotherapy, December 2000, p. 3357-3363, Vol. 44, No. 12
Institut für Molekulare
Infektionsbiologie, Röntgenring 11, D-97070
Würzburg,1 and
Robert-Koch-Institut, Bereich Wernigerode, Burgstraße 37,
D-38855 Wernigerode,2 Germany
Received 24 April 2000/Returned for modification 10 August
2000/Accepted 25 September 2000
Biofilm production is an important step in the pathogenesis of
Staphylococcus epidermidis polymer-associated infections
and depends on the expression of the icaADBC operon leading
to the synthesis of a polysaccharide intercellular adhesin. A
chromosomally encoded reporter gene fusion between the ica
promoter and the beta-galactosidase gene lacZ from
Escherichia coli was constructed and used to investigate
the influence of both environmental factors and subinhibitory
concentrations of different antibiotics on ica expression
in S. epidermidis. It was shown that S. epidermidis biofilm formation is induced by external stress
(i.e., high temperature and osmolarity). Subinhibitory concentrations
of tetracycline and the semisynthetic streptogramin antibiotic
quinupristin-dalfopristin were found to enhance ica
expression 9- to 11-fold, whereas penicillin, oxacillin,
chloramphenicol, clindamycin, gentamicin, ofloxacin, vancomycin, and
teicoplanin had no effect on ica expression. A weak (i.e.,
2.5-fold) induction of ica expression was observed for
subinhibitory concentrations of erythromycin. The results were
confirmed by Northern blot analyses of ica transcription and quantitative analyses of biofilm formation in a colorimetric assay.
0066-4804/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Effect of Subinhibitory Antibiotic Concentrations
on Polysaccharide Intercellular Adhesin Expression in
Biofilm-Forming Staphylococcus epidermidis
*
Corresponding author. Mailing address: Institut
für Molekulare Infektionsbiologie, Röntgenring 11, D-97070
Würzburg, Germany. Phone: 49-931-31-2154. Fax: 49-931-31-2578. E-mail: w.ziebuhr{at}mail.uni-wuerzburg.de.
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