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PMID: 10325322 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

The Calgary Biofilm Device: new technology for rapid determination of antibiotic susceptibilities of bacterial biofilms.

Journal of clinical microbiology ·Vol. 37 ·No. 6 ·1999-06-00 ·Pages 1771-6

Ceri H, Olson ME, Stremick C, Read RR, Morck D, Buret A

Abstract

Determination of the MIC, based on the activities of antibiotics against planktonic bacteria, is the standard assay for antibiotic susceptibility testing. Adherent bacterial populations (biofilms) present with an innate lack of antibiotic susceptibility not seen in the same bacteria grown as planktonic populations. The Calgary Biofilm Device (CBD) is described as a new technology for the rapid and reproducible assay of biofilm susceptibilities to antibiotics. The CBD produces 96 equivalent biofilms for the assay of antibiotic susceptibilities by the standard 96-well technology. Biofilm formation was followed by quantitative microbiology and scanning electron microscopy. Susceptibility to a standard group of antibiotics was determined for National Committee for Clinical Laboratory Standards (NCCLS) reference strains: Escherichia coli ATCC 25922, Pseudomonas aeruginosa ATCC 27853, and Staphylococcus aureus ATCC 29213. Growth curves demonstrated that biofilms of a predetermined size could be formed on the CBD at specific time points and, furthermore, that no significant difference (P > 0.1) was seen between biofilms formed on each of the 96 pegs. The antibiotic susceptibilities for planktonic populations obtained by the NCCLS method or from the CBD were similar. Minimal biofilm eradication concentrations, derived by using the CBD, demonstrated that for biofilms of the same organisms, 100 to 1,000 times the concentration of a certain antibiotic were often required for the antibiotic to be effective, while other antibiotics were found to be effective at the MICs. The CBD offers a new technology for the rational selection of antibiotics effective against microbial biofilms and for the screening of new effective antibiotic compounds.

MeSH Terms
Alberta Anti-Bacterial Agents/pharmacology Biofilms Escherichia coli/drug effects,growth & development,ultrastructure Laboratories/standards Microbial Sensitivity Tests/instrumentation,methods,standards Pseudomonas aeruginosa/drug effects,growth & development Quality Control Reproducibility of Results Sensitivity and Specificity Staphylococcus aureus/drug effects,growth & development
Chemicals
Anti-Bacterial Agents
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Ceri H
Biofilm Research Group, University of Calgary, Calgary, Alberta, Canada T2N 1N4. ceri@acs.ucalgary.ca
Olson M E
Stremick C
Read R R
Morck D
Buret A
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Article Info
Journal
Journal of clinical microbiology
Abbr.
J Clin Microbiol
ISSN
0095-1137
Published
1999-06-00
Pages
1771-6
Language
English
Region
United States
NLM ID
7505564
PMCID
PMC84946
Subset
IM
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