The authors are grateful to Yuki Kuboyama for her excellent technical assistance. All animal procedures were approved by the Committee on Animal Handling and Ethical Regulations of the National Institute of Infectious Diseases, Japan, and were undertaken in compliance with the guidelines issued from the Ministry of Health, Labor and Welfare, Japan. This work was supported by a Grant-in-Aid for Scientific
Research from the Ministry of Education, Science, Sports and Culture of Japan. This work was also supported in part by Grants-in-Aid from the Research Committee of Prion disease and Slow Virus Infection, the Ministry of Health, Labor and Welfare of Japan, and by grants from Research on Measures for Emerging and Reemerging infections (Intractable Infectious Diseases in Organ Transplant Recipients [H21-Shinko-Ippan-009]) of the Ministry of Health, Labor and Welfare of PFT�� Japan. “
“Bacterial biofilms have been observed in many prosthesis-related infections, and this mode of growth renders the infection both difficult to treat and especially difficult to detect and diagnose using standard culture methods. We (1) tested a novel coupled PCR-mass spectrometric (PCR-MS) assay (the Ibis T5000) on an ankle arthroplasty that was culture negative on preoperative aspiration and then (2) confirmed that the Ibis assay had in fact detected a viable multispecies biofilm by further selleck chemical micrographic and molecular examinations, including confocal
microscopy using Live/Dead stain, bacterial FISH, and reverse-transcriptase-PCR (RT-PCR) assay for bacterial Glutamate dehydrogenase mRNA. The Ibis technology detected Staphylococcus aureus, Staphylococcus epidermidis, and the methicillin resistance gene mecA in soft tissues associated with the explanted hardware. Viable S. aureus were confirmed using RT-PCR, and viable cocci in the biofilm configuration were detected microscopically on both tissue and hardware. Species-specific bacterial FISH confirmed a polymicrobial biofilm containing S. aureus. A novel culture method recovered S. aureus and S. epidermidis (both methicillin resistant) from
the tibial metal component. These observations suggest that molecular methods, particularly the new Ibis methodology, may be a useful adjunct to routine cultures in the detection of biofilm bacteria in prosthetic joint infection. Chronic infections following joint replacement are one example of the significant proportion of infections that are caused by bacteria growing in biofilms (Costerton et al., 1999). As a consequence of this protected mode of growth, these organisms are more resistant to antibiotics (Stewart & Costerton, 2001; Parsek & Singh, 2003) than their planktonic counterparts in acute infections, and are rarely resolved by host defense mechanisms (Costerton et al., 1999). Another feature of biofilm infections is their difficulty of detection using traditional culture methods (Veeh et al., 2003; Trampuz et al., 2007).