Cutibacterium acnes is less commonly identified by next-generation sequencing than culture in primary shoulder surgery

Introduction High rates of positive Cutibacterium acnes cultures from primary shoulder surgery make positive cultures in the revision surgery setting difficult to interpret. Our goal was to determine concordance between culture and next-generation sequencing techniques for identification of C. acnes from primary shoulder surgery. Methods Patients undergoing shoulder arthroscopy for rotator cuff tear or primary anatomic shoulder arthroplasty for osteoarthritis were prospectively enrolled. Specimens were sent for culture (aerobic and anaerobic) and next-generation sequencing. For next-generation sequencing, the entire microbial DNA was sequenced in order to identify pathogens within the sample. Results Our cohort consisted of 90 patients (45 patients in the osteoarthritis group and 45 patients in the rotator cuff tear group). At least one sample was positive for C. acnes in 18 (20%) cases by culture and in 14 (15.6%) cases by next-generation sequencing (p = 0.559). Four (22.2%) of the 18 cases with positive C. acnes cultures also had C. acnes identified by next-generation sequencing (kappa = 0.238). There was no difference in C. acnes identification rates between osteoarthritis and rotator cuff tear groups. Conclusions There was limited concordance between culture and next-generation sequencing for C. acnes identification. Further studies are needed to determine the potential for next-generation sequencing as a diagnostic tool.

[1]  J. Parvizi,et al.  Preoperative doxycycline does not decolonize Propionibacterium acnes from the skin of the shoulder: a randomized controlled trial. , 2017, Journal of shoulder and elbow surgery.

[2]  Gary L. Gallia,et al.  Next-generation sequencing in neuropathologic diagnosis of infections of the nervous system , 2016, Neurology: Neuroimmunology & Neuroinflammation.

[3]  P. Sethi,et al.  Presence of Propionibacterium acnes in primary shoulder arthroscopy: results of aspiration and tissue cultures. , 2015, Journal of shoulder and elbow surgery.

[4]  G. Huffman,et al.  Propionibacterium acnes infections in shoulder surgery. , 2014, The Orthopedic clinics of North America.

[5]  Roger E Bumgarner,et al.  Propionibacterium persists in the skin despite standard surgical preparation. , 2014, The Journal of bone and joint surgery. American volume.

[6]  S. Krishnan,et al.  Complications of Shoulder Arthroscopy , 2014, The Journal of the American Academy of Orthopaedic Surgeons.

[7]  Joseph L DeRisi,et al.  Actionable diagnosis of neuroleptospirosis by next-generation sequencing. , 2014, The New England journal of medicine.

[8]  O. Levy,et al.  Propionibacterium acnes: an underestimated etiology in the pathogenesis of osteoarthritis? , 2013, Journal of shoulder and elbow surgery.

[9]  M. Neradilek,et al.  Prognostic factors for bacterial cultures positive for Propionibacterium acnes and other organisms in a large series of revision shoulder arthroplasties performed for stiffness, pain, or loosening. , 2012, The Journal of bone and joint surgery. American volume.

[10]  J. Rakeman,et al.  Optimization of Periprosthetic Culture for Diagnosis of Propionibacterium acnes Prosthetic Joint Infection , 2011, Journal of Clinical Microbiology.

[11]  B. Haas,et al.  Chimeric 16S rRNA sequence formation and detection in Sanger and 454-pyrosequenced PCR amplicons. , 2011, Genome research.

[12]  Robert C. Edgar,et al.  Search and clustering orders of magnitude faster than BLAST , 2010, Bioinform..

[13]  K. McColl Clinical practice. Helicobacter pylori infection. , 2010, The New England journal of medicine.

[14]  E. Craig,et al.  Propionibacterium acnes infection after shoulder arthroplasty: a diagnostic challenge. , 2010, Journal of shoulder and elbow surgery.

[15]  S. Suerbaum,et al.  Helicobacter pylori infection , 2013, Nature Reviews Disease Primers.

[16]  D. Fredricks,et al.  Sequencing and Analysis of Fungal rRNA Operons for Development of Broad-Range Fungal PCR Assays , 2009, Applied and Environmental Microbiology.

[17]  J. Clarridge,et al.  Impact of 16S rRNA Gene Sequence Analysis for Identification of Bacteria on Clinical Microbiology and Infectious Diseases , 2004, Clinical Microbiology Reviews.