Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2012 Sep;56(9):4976-9.
doi: 10.1128/AAC.00650-12. Epub 2012 Jul 9.

Mature Pseudomonas aeruginosa biofilms prevail compared to young biofilms in the presence of ceftazidime

Affiliations

Mature Pseudomonas aeruginosa biofilms prevail compared to young biofilms in the presence of ceftazidime

Laura L Bowler et al. Antimicrob Agents Chemother. 2012 Sep.

Abstract

Phenotypic tolerances to antibiotics of mature and young Pseudomonas aeruginosa PAO1 biofilms and released planktonic bacteria were compared for four antibiotics. Resistance levels were similar for gentamicin and ciprofloxacin but differed for ceftazidime and meropenem. β-Lactamase mapping showed that, after 5 h of ceftazidime exposure, mature biofilms produced more β-lactamase than young biofilms, facilitating the growth of released planktonic bacteria. This shows the importance of early treatment and choice of antibiotics for P. aeruginosa biofilm infections.

PubMed Disclaimer

Figures

Fig 1
Fig 1
Antibiotic susceptibilities of a young (4-h) biofilm (a) and a mature (24-h) biofilm (b), showing the log-transformed MBEC of the biofilm and the MIC and MBC values of the bacteria released from the biofilm following 24 h exposure to antibiotics.
Fig 2
Fig 2
β-Lactamase activity from young (4-h) and mature (24-h) biofilms and levels of their released planktonic bacteria and the supernatant per indicated protein concentration after 5 h (a) and 24 h (b) of antibiotic exposure. All values represent the averages of the results of three replicate experiments, with error bars indicating standard errors. * indicates a significant difference between the results of 5-h and 24-h antibiotic exposure, and ** indicates a significant difference between the results determined for young and mature biofilms (P < 0.05).

References

    1. Bagge N, et al. 2004. Dynamics and spatial distribution of β-lactamase expression in Pseudomonas aeruginosa biofilms. Antimicrob. Agents Chemother. 48:1168–1174 doi: - DOI - PMC - PubMed
    1. Bagge N, et al. 2004. Pseudomonas aeruginosa biofilms exposed to imipenem exhibit changes in global gene expression and β-lactamase and alginate production. Antimicrob. Agents Chemother. 48:1175–1187 doi: - DOI - PMC - PubMed
    1. Baquero F, Vicente MF, Perez-Diaz JC. 1985. β-Lactam coselection of sensitive and TEM-1 β-lactamase-producing subpopulations in heterogeneous Escherichia coli colonies. J. Antimicrob. Chemother. 15:151–157 - PubMed
    1. Ceri H, Olson ME, Stremick C, Read RR, Morck D. 1999. The Calgary Biofilm Device: new technology for rapid determination of antibiotic susceptibilities. J. Clin. Microbiol. 37:1771–1776 - PMC - PubMed
    1. De Kievit TR, et al. 2001. Multidrug efflux pumps: expression patterns and contribution to antibiotic resistance in Pseudomonas aeruginosa biofilms. Antimicrob. Agents Chemother. 45:1761–1770 doi: - DOI - PMC - PubMed

Publication types

MeSH terms