J Med Microbiol International Journal of Systematic and Evolutionary Microbiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Stickler, D. J.
Right arrow Articles by Morgan, S. D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Stickler, D. J.
Right arrow Articles by Morgan, S. D.
Agricola
Right arrow Articles by Stickler, D. J.
Right arrow Articles by Morgan, S. D.
J Med Microbiol 55 (2006), 489-494; DOI: 10.1099/jmm.0.46404-0
© 2006 Society for General Microbiology
ISSN 1473-5644

Modulation of crystalline Proteus mirabilis biofilm development on urinary catheters

David J. Stickler and Sheridan D. Morgan

Cardiff School of Biosciences, Cardiff University, Cardiff CF10 3TL, UK

Correspondence
David J. Stickler
stickler{at}cardiff.ac.uk

Received 7 November 2005
Accepted 10 January 2006


The crystalline biofilms formed by Proteus mirabilis can seriously complicate the care of patients undergoing long-term bladder catheterization. The generation of alkaline urine by the bacterial urease causes calcium and magnesium phosphates to precipitate from urine and accumulate in the catheter biofilm, blocking the flow of urine from the bladder. The pH at which these salts crystallize from a urine sample, the nucleation pH (pHn), can be elevated by diluting the urine and by increasing its citrate content. The aim of this study was to examine whether manipulation of pHn in these ways modulated the rate at which crystalline biofilm developed. Experiments in laboratory models of the catheterized bladder infected with P. mirabilis showed that when the bladder was supplied with a concentrated urine (pHn 6·7) at a low fluid output (720 ml per 24 h), catheters blocked at 19–31 h. Diluting this urine 1 : 4 increased the pHn to 7·5 and models supplied with this urine at 2880 ml per 24 h took 110–137 h to block. When models were supplied with urine containing citrate at 1·5 mg ml–1 or above (pHn 8·3–9·1), the catheters drained freely for the full 7 day experimental period. Scanning electron microscopy revealed that the catheter biofilms that developed in urine with high pHn values were devoid of crystalline formations. These observations should encourage a clinical trial to examine the effect of increasing a patient's fluid intake with citrate-containing drinks on the encrustation and blockage of catheters.




This article has been cited by other articles:


Home page
Clin. Microbiol. Rev.Home page
S. M. Jacobsen, D. J. Stickler, H. L. T. Mobley, and M. E. Shirtliff
Complicated Catheter-Associated Urinary Tract Infections Due to Escherichia coli and Proteus mirabilis
Clin. Microbiol. Rev., January 1, 2008; 21(1): 26 - 59.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL J MED MICROBIOL MICROBIOLOGY J GEN VIROL ALL SGM JOURNALS
Copyright © 2006 Society for General Microbiology.