Laboratory of Infectious Agents and Hygiene, University Hospital of St-Etienne, St-Etienne, France.
CIRI, Centre International de Recherche en Infectiologie, GIMAP team, University of Lyon, University of St-Etienne, INSERM, U1111, CNRS UMR5308, ENS de Lyon, UCBL, St-Etienne, France.
J Clin Microbiol. 2022 Jan 19;60(1):e0083521. doi: 10.1128/JCM.00835-21. Epub 2021 Nov 17.
Bone and joint infections represent a potentially devastating complication of prosthetic orthopedic joint replacement, thus requiring both rapid and appropriate antibiotic treatment. Staphylococcus aureus is one of the most common pathogens involved in this pathology. Being able to assert its presence is the first step of efficient patient management. This monocenter study evaluated the MRSA/SA ELITe MGB assay for the molecular detection of S. aureus and methicillin-resistant S. aureus (MRSA) in bone and joint biopsy specimens and synovial fluids. This test, together with conventional techniques, including standard cultures and the 16S rRNA amplification assay, was performed on 208 successive perioperative samples collected prospectively for 1 year obtained from 129 patients. Using conventional techniques, we detected a microbial pathogen in 76 samples from 58 patients, 40 of which were identified as S. aureus. The limit of detection (LOD) of the MRSA/SA ELITe MGB assay was experimentally determined for bone and joint biopsy specimens and synovial fluids using negative samples spiked with S. aureus ATCC 43300. The sensitivities of S. aureus detection with the MRSA/SA ELITe MGB assay were 82.5% (33/40 samples) and 97.5% (39/40 samples) using the manufacturer's LOD and an experimentally determined LOD, respectively. Interestingly, using the osteoarticular specific LOD, 15 additional samples were determined to be positive for S. aureus DNA with the MRSA/SA ELITe MGB assay; in all cases, these samples were obtained from patients considered to be infected with S. aureus according to their clinical and microbiological records. The results were available within 24 h, which could help to expedite therapeutic decisions.
骨和关节感染是人工关节置换术后一种潜在的破坏性并发症,因此需要快速和适当的抗生素治疗。金黄色葡萄球菌是这种病理中最常见的病原体之一。能够确定其存在是有效患者管理的第一步。这项单中心研究评估了 MRSA/SA ELITe MGB 测定法,用于检测骨和关节活检标本和滑液中的金黄色葡萄球菌和耐甲氧西林金黄色葡萄球菌(MRSA)。该检测方法与常规技术(包括标准培养和 16S rRNA 扩增检测)一起,对 129 名患者的 208 例连续围手术期样本进行了前瞻性检测,这些样本在 1 年内收集。使用常规技术,我们从 58 名患者的 76 份样本中检测到微生物病原体,其中 40 份鉴定为金黄色葡萄球菌。使用阴性样本(金黄色葡萄球菌 ATCC 43300 污染),通过实验确定了 MRSA/SA ELITe MGB 测定法检测骨和关节活检标本和滑液中微生物病原体的检测限(LOD)。使用制造商的 LOD 和实验确定的 LOD,MRSA/SA ELITe MGB 检测法检测金黄色葡萄球菌的灵敏度分别为 82.5%(33/40 份样本)和 97.5%(39/40 份样本)。有趣的是,使用骨关节炎特异性 LOD,MRSA/SA ELITe MGB 检测法还检测到 15 份额外的金黄色葡萄球菌 DNA 阳性样本;在所有情况下,这些样本均来自根据临床和微生物记录认为金黄色葡萄球菌感染的患者。结果可在 24 小时内获得,这有助于加快治疗决策。