A total of 212 coagulase-negative Staphylococcus strains recovered prospectively during 119 surgeries for proven or suspected bone and joint infection (BJI) were identified by sodA sequencing. These strains were identified as 151 Staphylococcus epidermidis isolates, 15 S. warneri isolates, 14 S. capitis isolates, 9 S. hominis isolates, 6 S. lugdunensis isolates, 5 S. haemolyticus isolates, 4 S. caprae isolates, 4 S. pasteuri isolates, 3 S. simulans isolates, and 1 S. cohnii isolate. Only S. epidermidis, S. lugdunensis, S. capitis, and S. caprae were found to be infecting organisms and were involved, respectively, in 35 (81.4%), 3 (7.0%), 3 (7.0%), and 2 (4.6%) cases of BJI.Coagulase-negative Staphylococcus (CoNS) strains are a leading cause of arthroplastic infections, accounting for 15 to 37.5% of isolates recovered from peroperative samples (13). Staphylococcus epidermidis is the main species responsible for these infections and for other device-related bone and joint infections (BJI). There are some reports of true BJI caused by CoNS species other than S. epidermidis, including S. caprae (1), S. lugdunensis (24), and S. simulans (18). However, no prospective study has specifically addressed the species distribution of CoNS strains in BJI. Identification of CoNS strains to the species level has long been an obstacle preventing this question from being answered satisfactorily. PCR-based sequencing methods can now accurately identify a wide spectrum of Staphylococcus species (7,11,17). In this 4-year prospective study, we used sodA sequencing to identify CoNS species associated with BJI.All surgical procedures performed in the orthopedic department of Raymond Poincaré hospital (Garches, France) between January 1999 and December 2002 for proven or suspected BJI were studied prospectively. We included all procedures in which at least three independent samples were collected during the same operative procedure, at least one sample was positive for a CoNS strain, and no samples were positive for organisms other than CoNS strains. The samples were processed in a class 2 laminar-flow safety cabinet. A portion of the sample was Gram stained, and the remainder was used to inoculate 10 ml of Schaedler broth (BioMérieux, Marcy l'Etoile, France). After agitation, aliquots were used to inoculate chocolate agar plates (incubated in 5% CO 2 ) and blood agar plates (incubated aerobically and anaerobically). The plates were examined daily for 7 days. Broths were subcultured after 1 and 5 days. The "CoNS group" was identified by Gram staining, catalase testing, Slidex latex agglutination testing (BioMérieux), and tube coagulase testing (Bio-Rad, Marnes la Coquette, France). Antibiotic susceptibility was evaluated by the disk diffusion method on Mueller-Hinton agar (Bio-Rad). Strains were identified to the species level by partial sodA sequencing (17) as described recently by our group (21). We used the definitions and criteria recommended by the OSIRIS (Oxford Skeletal Infection Research and Intervention Service) group (2). CoNS...