We report the case of a total hip arthroplasty infection caused by Ruminococcus gnavus in a 62-year-old man with ulcerative colitis. The bacterium was perfectly identified by matrix-assisted laser desorption ionization-time of flight mass spectrometry.
CASE REPORTA 62-year-old man was referred to the orthopedic surgery department of a suburban clinic with suspected prosthetic joint infection (PJI) of the right hip. This patient had undergone total right hip replacement 13 years earlier and had shown no signs of prosthesis dysfunction since surgery.On admission, the patient presented with right hip pain and fever. Biological tests showed elevated white blood cell (18.3 ϫ 10 9 cells/liter) and C-reactive protein (137 mg/liter) levels. No blood culture was collected. Radiological evaluation of the total hip arthroplasty showed a 5-mm subsidence of the femoral stem.Three bone biopsies were performed with a notch needle, and the samples were sent to the microbiology laboratory of the Hôpi-taux Universitaires Paris Ile de France Ouest, Greater Paris, for microbiological analysis. Samples were processed as previously described (1), with continuously monitored broth enrichment. Briefly, samples were topped with 17 ml sterile distilled water and bead milled for 150 s on a Retsch MM300 mixer mill (Verder, France) with 10 to 15 5-mm-diameter stainless steel beads. One hundred microliters of the resulting suspension, plated on 5% sheep blood Columbia agar medium, was incubated for 5 days at 36°C under aerobic and anaerobic conditions, and 6 ml was injected into Bactec Peds Plus and Lytic/10 Anaerobic/F blood culture vials supplemented with a fastidious organism supplement incubated for 14 days in a Bactec FX automated blood culture system (BD Diagnostics, Le Pont de Claies, France). Microscopic examination of the three biopsy samples showed an absence of erythrocytes, numerous polymorphonuclear cells, and Grampositive cocci in short chains. No empirical antibiotic therapy was started after the biopsy. All samples yielded positive cultures on anaerobic medium, with a time to detection of 7 h 7 min for all three Lytic/10 Anaerobic/F vials. On day 1, growth was detected on anaerobic blood agar plates, with numerous translucent small colonies. The diplococci were identified by mass spectrometry (Biotyper version 3.1 on a Microflex LT mass spectrometer, Bruker Daltonics, Bremen, Germany) as Ruminococcus gnavus, with a score of 2.2, and later confirmed by 16S rRNA gene sequencing using previously described primers (2). A 16S rRNA gene fragment of 407 bp was amplified from the bacteria and sequenced on an Applied Biosystems genetic analyzer. GenBank database searches showed the amplified sequences to be 99% (404/ 407 bp) identical to the 16S rRNA gene sequence of the reference strain for R. gnavus ATCC 29149 (GenBank accession no. KP407134). Antimicrobial susceptibility testing by the agar disk diffusion method (Bio-Rad, Marnes-la-Coquette, France) using Comité de l'Antibiogramme de la Société Française de Microbiologie (CA-SFM 20...