Clinical Use of a 16S Ribosomal RNA Gene-Based Sanger and/or Next Generation Sequencing Assay to Test Preoperative Synovial Fluid for Periprosthetic Joint Infection Diagnosis.


Journal

mBio
ISSN: 2150-7511
Titre abrégé: mBio
Pays: United States
ID NLM: 101519231

Informations de publication

Date de publication:
20 12 2022
Historique:
entrez: 10 11 2022
pubmed: 11 11 2022
medline: 3 3 2023
Statut: ppublish

Résumé

Preoperative pathogen identification in patients with periprosthetic joint infection (PJI) is typically limited to synovial fluid culture. Whether sequencing-based approaches are of potential use in identification of pathogens in PJI, and if so which approach is ideal, is incompletely defined. The objective of the study was to analyze the accuracy of a 16S rRNA (rRNA) gene-based PCR followed by Sanger sequencing and/or targeted metagenomic sequencing approach (tMGS) performed on synovial fluid for PJI diagnosis. A retrospective study was conducted, analyzing synovial fluids tested between August 2020 and May 2021 at a single center. Subjects with hip, knee, shoulder, and elbow arthroplasties who had synovial fluid aspirated and clinically subjected to sequence-based testing and conventional culture were studied. A total of 154 subjects were included in the study; 118 had noninfectious arthroplasty failure (NIAF), while 36 had PJI. Clinical sensitivity and specificity for diagnosis of PJI were 69% and 100%, respectively, for the sequencing-based approach and 72% and 100%, respectively, for conventional culture (

Identifiants

pubmed: 36354331
doi: 10.1128/mbio.01322-22
pmc: PMC9765659
doi:

Substances chimiques

RNA, Ribosomal, 16S 0
Biomarkers 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0132222

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Auteurs

Laure Flurin (L)

Division of Clinical Microbiology, Department of Laboratory Medicine and Pathology, Mayo Clinicgrid.66875.3a, Rochester, Minnesota, USA.
Department of Intensive Care, University Hospital of Guadeloupe, Pointe-à-Pitre, France.

Joseph J Hemenway (JJ)

Division of Clinical Microbiology, Department of Laboratory Medicine and Pathology, Mayo Clinicgrid.66875.3a, Rochester, Minnesota, USA.

Cody R Fisher (CR)

Division of Clinical Microbiology, Department of Laboratory Medicine and Pathology, Mayo Clinicgrid.66875.3a, Rochester, Minnesota, USA.

James J Vaillant (JJ)

Division of Clinical Microbiology, Department of Laboratory Medicine and Pathology, Mayo Clinicgrid.66875.3a, Rochester, Minnesota, USA.
Division of Public Health, Infectious Diseases and Occupational Medicine, Department of Medicine, Mayo Clinicgrid.66875.3a, Rochester, Minnesota, USA.

Marisa Azad (M)

Division of Clinical Microbiology, Department of Laboratory Medicine and Pathology, Mayo Clinicgrid.66875.3a, Rochester, Minnesota, USA.
Division of Public Health, Infectious Diseases and Occupational Medicine, Department of Medicine, Mayo Clinicgrid.66875.3a, Rochester, Minnesota, USA.

Matthew J Wolf (MJ)

Division of Clinical Microbiology, Department of Laboratory Medicine and Pathology, Mayo Clinicgrid.66875.3a, Rochester, Minnesota, USA.

Kerryl E Greenwood-Quaintance (KE)

Division of Clinical Microbiology, Department of Laboratory Medicine and Pathology, Mayo Clinicgrid.66875.3a, Rochester, Minnesota, USA.

Matthew P Abdel (MP)

Department of Orthopedic Surgery, Mayo Clinicgrid.66875.3a, Rochester, Minnesota, USA.

Robin Patel (R)

Division of Clinical Microbiology, Department of Laboratory Medicine and Pathology, Mayo Clinicgrid.66875.3a, Rochester, Minnesota, USA.

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Classifications MeSH