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1 June 2007

Volume 195, Number 11
The Journal of Infectious Diseases 2007;195:1705–1712
0022-1899/2007/19511-0020$15.00
DOI: 10.1086/517522
MAJOR ARTICLE

β‐1,3 Glucan as a Test for Central Venous Catheter Biofilm Infection

Jeniel Nett,

Leslie Lincoln,

Karen Marchillo, and

David Andes

Departments of Medicine and of Medical Microbiology and Immunology, University of Wisconsin, Madison

Biofilms are microbial communities that are associated with solid surfaces such as intravascular catheters. Candida species are a major cause of medical device–associated infections. Twenty percent to 70% of all candidemias are associated with this biofilm process. Diagnosis and effective treatment of Candida device‐associated infections requires removal of the involved device. The ability to identify a biofilm device infection before catheter removal may obviate removal of a substantial number of devices. Prior studies in our laboratory identified cell wall changes (specifically, increased β‐1,3 glucan) associated with biofilm, compared with planktonic C. albicans. Both in vitro and in vivo (catheter) biofilm models were used to determine whether biofilm cells secreted more β‐1,3 glucan and whether these differences could be used to discern the presence of a Candida biofilm infection with 3 species (C. albicans, C. glabrata, and C. parapsilosis). A limulus lysate assay was used to quantify β‐1,3 glucan in supernatants from planktonic or biofilm cultures and in the serum of rats with an intravascular catheter biofilm infection or disseminated candidiasis. β‐1,3 glucan was detected from both in vitro and in vivo models from each condition. However, the concentrations of β‐1,3 glucan from the biofilm conditions were 4–10‐fold greater in vitro ( ) and were 10‐fold greater in vivo ( ), despite equal or fewer numbers of cells in the biofilm conditions. These results suggest the secreted polysaccharide β‐1,3 glucan may serve as a useful tool for the diagnosis of Candida biofilm and device‐associated infections.

Received 30 October 2006; accepted 21 December 2006; electronically published 17 April 2007.

Reprints or correspondence: Dr. David Andes, 600 Highland Ave., Rm. H4.572, Madison, WI 53792 ().

Cited by

Jeniel E. Nett, Alexander J. Lepak, Karen Marchillo, and David R. Andes. (2009) Time Course Global Gene Expression Analysis of an In Vivo Candida Biofilm. The Journal of Infectious Diseases 200:2, 307-313
Online publication date: 15-Jul-2009.
Jeniel E. Nett, David Andes. (2009) Review of techniques for diagnosis of catheter-related Candida biofilm infections. Current Fungal Infection Reports 2:4, 237-243
Online publication date: 1-Jan-2009.
CrossRef
Ana Laín, Natalia Elguezabal, María Dolores Moragues, Juan Carlos García-Ruiz, Amalia del Palacio, José Pontón. (2008) Contribution of serum biomarkers to the diagnosis of invasive candidiasis. Expert Review of Molecular Diagnostics 8:3, 315-325
Online publication date: 1-Jun-2008.
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Joseph M Fritz, Benjamin D Brielmaier, Erik R Dubberke. (2008) Micafungin for the prophylaxis and treatment of Candida infections. Expert Review of Anti-infective Therapy 6:2, 153-162
Online publication date: 1-May-2008.
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L. Joseph Wheat. (2007) Nonculture diagnostic methods for invasive fungal infections. Current Infectious Disease Reports 9:6, 465-471
Online publication date: 1-Dec-2007.
CrossRef
  • Potential conflicts of interest: none reported.

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