Volume 16, Issue 1 pp. 37-44

Biofilms in chronic wounds

Garth A. James PhD

Garth A. James PhD

Center for Biofilm Engineering, Montana State University-Bozeman, Bozeman, Montana, and

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Ellen Swogger BS

Ellen Swogger BS

Center for Biofilm Engineering, Montana State University-Bozeman, Bozeman, Montana, and

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Randall Wolcott MD

Randall Wolcott MD

Southwest Regional Wound Care Center, Lubtock, Texas

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Elinor deLancey Pulcini PhD

Elinor deLancey Pulcini PhD

Center for Biofilm Engineering, Montana State University-Bozeman, Bozeman, Montana, and

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Patrick Secor BS

Patrick Secor BS

Center for Biofilm Engineering, Montana State University-Bozeman, Bozeman, Montana, and

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Jennifer Sestrich BS

Jennifer Sestrich BS

Center for Biofilm Engineering, Montana State University-Bozeman, Bozeman, Montana, and

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John W. Costerton PhD

John W. Costerton PhD

Center for Biofilm Engineering, Montana State University-Bozeman, Bozeman, Montana, and

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Philip S. Stewart PhD

Philip S. Stewart PhD

Center for Biofilm Engineering, Montana State University-Bozeman, Bozeman, Montana, and

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First published: 13 December 2007
Citations: 1,185
Reprint requests:
Garth James, Center for Biofilm Engineering, 366 EPS Building, Montana State University, Bozeman, Montana 59717.
Tel: 406-994-2542;
Fax: 406-994-6098;
Email: [email protected]

ABSTRACT

Chronic wounds including diabetic foot ulcers, pressure ulcers, and venous leg ulcers are a worldwide health problem. It has been speculated that bacteria colonizing chronic wounds exist as highly persistent biofilm communities. This research examined chronic and acute wounds for biofilms and characterized microorganisms inhabiting these wounds. Chronic wound specimens were obtained from 77 subjects and acute wound specimens were obtained from 16 subjects. Culture data were collected using standard clinical techniques. Light and scanning electron microscopy techniques were used to analyze 50 of the chronic wound specimens and the 16 acute wound specimens. Molecular analyses were performed on the remaining 27 chronic wound specimens using denaturing gradient gel electrophoresis and sequence analysis. Of the 50 chronic wound specimens evaluated by microscopy, 30 were characterized as containing biofilm (60%), whereas only one of the 16 acute wound specimens was characterized as containing biofilm (6%). This was a statistically significant difference (p<0.001). Molecular analyses of chronic wound specimens revealed diverse polymicrobial communities and the presence of bacteria, including strictly anaerobic bacteria, not revealed by culture. Bacterial biofilm prevalence in specimens from chronic wounds relative to acute wounds observed in this study provides evidence that biofilms may be abundant in chronic wounds.

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