Flocked swabs (Copan) were compared to rayon swabs (Copan) for the nasal detection of Staphylococcus aureus in 90 healthy volunteers sampled sequentially during a 5-week period. The use of flocked swabs improved the number of nasal carriers (P ؍ 0.026), the number of positive specimens (P ؍ 0.01), and the quantity of bacteria in positive samples (P ؍ 0.004).Staphylococcus aureus nasal carriage is a major risk factor for S. aureus infection, and the anterior nares are the primary reservoir of S. aureus in humans (19). Therefore, it is desirable to optimize S. aureus detection and to establish the carriage status, particularly in the aim of prophylactically decolonizing patients at risk of infection with this bacterium (4).The detection of S. aureus carriage is usually carried out by nasal sampling. In comparison to the use of rayon swabs, the use of flocked swabs has been demonstrated to improve the uptake of epithelial cells and viruses (1, 7), to release more microorganisms in vitro (18), and to enhance the molecular detection of Chlamydia trachomatis and Neisseria gonorrhoeae (6). Despite these apparent advantages, a recent study that compared flocked and rayon swabs after a 24-h broth culture enrichment did not show any difference in the rate detection of S. aureus nasal carriers (8). To further assess the utility of flocked swabs, we conducted a study similar to that mentioned just above, with the exception that no enrichment step was performed.Ninety healthy health care workers from the University Hospital of Saint-Etienne, France, were included in the study from March to April 2010. Each volunteer was sampled 7 times with flocked and rayon swabs during a 5-week period (2 volunteers missed the seventh sampling). The study received the approval of our regional ethical research committee (Comité de Protection des Personnes Sud-Est I).A total of 628 nylon swabs (regular flocked swabs, reference 552C; Copan, Brescia, Italy) and 628 rayon swabs (standard swabs with Amies agar gel, reference 108C; Copan) were used by a unique trained fellow by following a predefined protocol (5). Swabs were wetted in normal saline, introduced into the anterior nostril, and rotated 5 times. During each sampling episode, one nostril was randomly sampled with a flocked swab, and the other was sampled with a rayon swab. Each swab was immediately placed into 1 ml of phosphate-buffered saline before being Vortex mixed for 10 s, and 50 l of this solution was plated onto a chromogenic medium (BBL CHROMagar Staph aureus; Becton Dickinson). After 24 h and 48 h of growth at 37°C, plates were read, and pink colonies were plated onto blood agar. Matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS; Bruker Daltonics, Bremen, Germany) was used for bacterial identification (9). After 48 h of growth, the number of pink colonies present on the chromogenic medium was determined, according to standard counting procedure, and expressed in CFU/ml. SPSS software (version 16.0, Chicago, IL) was used for statis...