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PMID: 2893804 Published · ppublish English Journal Article

Quantitation of effects of subinhibitory concentrations of trimethoprim on P fimbria expression and in vitro adhesiveness of uropathogenic Escherichia coli.

Journal of clinical microbiology ·Vol. 26 ·No. 1 ·1988-01-00 ·Pages 25-30

Dean EA, Kessler RE

Abstract

The ability to adhere to and colonize urogenital mucosa is an important virulence attribute of uropathogenic Escherichia coli. This adherence, which appears to be mediated by P fimbriae, may be affected by antibiotics or other agents that affect fimbrial expression. We describe here an enzyme immunofiltration assay to quantitate fimbriation and the application of that technique to measurement of the effects of sublethal doses of trimethoprim on P fimbrial expression. Effects on P fimbriation correlated with effects on the adherence of treated bacteria to cultured T24 bladder carcinoma epithelial cells; i.e., trimethoprim treatment decreased both P fimbriation and bacterial adherence. It was possible to quantitate effects on P fimbriation when type 1 fimbriae were also present. The enzyme immunofiltration assay may be useful for studies on the role of fimbriae in the pathogenesis of bacterial infections, and it may facilitate identification of antimicrobial agents that interfere with bacterial adherence to mucosal surfaces.

MeSH Terms
Bacterial Adhesion/drug effects Epithelium/microbiology Escherichia coli/drug effects,physiology,ultrastructure Fimbriae, Bacterial/drug effects,immunology Humans Immunoassay Trimethoprim/pharmacology Tumor Cells, Cultured Urinary Bladder/microbiology
Chemicals
Trimethoprim
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Dean E A
Pharmaceutical Research and Development Division, Bristol-Myers Company, Wallingford, Connecticut 06492.
Kessler R E
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Article Info
Journal
Journal of clinical microbiology
Abbr.
J Clin Microbiol
ISSN
0095-1137
Published
1988-01-00
Pages
25-30
Language
English
Region
United States
NLM ID
7505564
PMCID
PMC266171
Subset
IM
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