Effect of subinhibitory antibiotic concentrations on polysaccharide intercellular adhesin expression in biofilm-forming Staphylococcus epidermidis

被引:288
作者
Rachid, S
Ohlsen, K
Witte, W
Hacker, J
Ziebuhr, W
机构
[1] Inst Mol Infekt Biol, D-97070 Wurzburg, Germany
[2] Robert Koch Inst, Bereich Wernigerode, D-38855 Wernigerode, Germany
关键词
D O I
10.1128/AAC.44.12.3357-3363.2000
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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 Ii-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 far 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.
引用
收藏
页码:3357 / 3363
页数:7
相关论文
共 56 条
[41]   Effect of subinhibitory concentrations of vancomycin, cefazolin, ofloxacin, L-ofloxacin and D-ofloxacin on adherence to intravascular catheters and biofilm formation by Staphylococcus epidermidis [J].
Rupp, ME ;
Hamer, KE .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1998, 41 (02) :155-161
[42]   COAGULASE-NEGATIVE STAPHYLOCOCCI - PATHOGENS ASSOCIATED WITH MEDICAL PROGRESS [J].
RUPP, ME ;
ARCHER, GL .
CLINICAL INFECTIOUS DISEASES, 1994, 19 (02) :231-243
[43]  
Sambrook J., 1989, MOL CLONING
[44]   DNA SEQUENCING WITH CHAIN-TERMINATING INHIBITORS [J].
SANGER, F ;
NICKLEN, S ;
COULSON, AR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1977, 74 (12) :5463-5467
[45]  
SCHENK S, 1992, FEMS MICROBIOL LETT, V94, P133
[46]   Impact of bacterial biofilm formation on in vitro and in vivo activities of antibiotics [J].
Schwank, S ;
Rajacic, Z ;
Zimmerli, W ;
Blaser, J .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1998, 42 (04) :895-898
[47]   Thinking about bacterial populations as multicellular organisms [J].
Shapiro, JA .
ANNUAL REVIEW OF MICROBIOLOGY, 1998, 52 :81-104
[48]   GROWTH-CHARACTERISTICS OF GROUP-A STREPTOCOCCI IN A NEW CHEMICALLY DEFINED MEDIUM [J].
VANDERIJN, I ;
KESSLER, RE .
INFECTION AND IMMUNITY, 1980, 27 (02) :444-448
[49]   The effects of adherence to silicone surfaces on antibiotic susceptibility in Staphylococcus aureus [J].
Williams, I ;
Venables, WA ;
Lloyd, D ;
Paul, F ;
Critchley, I .
MICROBIOLOGY-UK, 1997, 143 :2407-2413
[50]   Antibiotic resistance in Gram-positive bacteria: epidemiological aspects [J].
Witte, W .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1999, 44 :1-9