Miniaturized oligonucleotide arrays: a new tool for discriminating colonization from infection due to Staphylococcus aureus in diabetic foot ulcers
- Albert Sotto, MD, PhD1,
- Richard Jean-Louis, MD2,
- Nathalie Jourdan, MD3,
- Christophe Combescure, PhD4,
- Nicole Bouziges, MD1,,5 and
- Jean-Philippe Lavigne, MD, PhD (jean.philippe.lavigne{at}chu-nimes.fr) on the behalf of the Nîmes University Hospital Working Group on the Diabetic Foot (GP30)1,,5
- 1Institut National de la Santé et de la Recherche Médicale, ESPRI 26, Université de Montpellier 1, UFR de Médecine, Avenue Kennedy, 30908 Nîmes cedex 02, France
- 2Service des Maladies de la Nutrition et de Diabétologie, CHU de Nîmes, 30240 Le Grau du Roi, France
- 3Service des Maladies Métaboliques et Endocriniennes, Groupe Hospitalo-Universitaire Carémeau, Place du Professeur Robert Debré, 30029 Nîmes Cedex 9, France
- 4Département de l'Information Médicale, Groupe Hospitalo-Universitaire Carémeau, Place du Professeur Robert Debré, 30029 Nîmes Cedex 9, France
- 5Laboratoire de Bactériologie, Groupe Hospitalo-Universitaire Carémeau, Place du Professeur Robert Debré, 30029 Nîmes Cedex 9, France
Abstract
OBJECTIVE - To evaluate the use of oligonucleotide arrays to discriminate colonization from infection due to Staphylococcus aureus in diabetic foot ulcers.
RESEARCH DESIGN AND METHODS - We included diabetic patients hospitalized in a diabetic foot department for an episode of foot ulcer. Only patients who had no antibiotic treatment during the previous 6-month were included. At admission, ulcers were classified on clinical examination, according to the IDSA system. 72 patients with culture positive only for S. aureus as the sole pathogen were included. In individuals with a grade 1 ulcer, a second wound bacterial specimen was obtained one month later. Using oligonucleotide arrays, S. aureus resistance and virulence genes were compared between grade 1 and grade 2-4 ulcers.
RESULTS - S. aureus was initially isolated from 22 grade 1 and 50 grade 2-4 ulcers: 35 were methicillin-resistant and 37 methicillin-sensitive. In 20 grade 1 ulcers (92%), no virulence genes were identified whereas these genes were present in all but one grade 2-4 ulcers. During follow-up, the two grade 1 ulcers which infected with strains carrying virulence genes rapidly deteriored: the array technology showed unchanged genotype profiles. On the contrary, two grade 1 ulcers healed: the genotype profiles were different from those at inclusion but without appearance of virulence genes.
CONCLUSIONS - The DNA array appears as a promising technique, easy to perform. Our observational study suggests that it might help distinguish colonized grade 1 from infected grade 2 wounds, predict ulcer outcome and contribute to a more adequate use of antibiotics.
Footnotes
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- Received March 8, 2007.
- Accepted April 24, 2007.
- Copyright © American Diabetes Association














