Center for Musculoskeletal Research, University of Rochester Medical Center, Rochester, New York, USA.
Department of Orthopaedics and Rehabilitation, University of Rochester Medical Center, Rochester, New York, USA.
J Orthop Res. 2021 Oct;39(10):2141-2150. doi: 10.1002/jor.24935. Epub 2020 Dec 15.
Staphylococcus aureus and Streptococcus agalactiae (Group B streptococcus, GBS) are common causes of deep musculoskeletal infections (MSKI) and result in significant patient morbidity and cost to the healthcare system. One of the major challenges with MSKI is the lack of faithful diagnostics to correctly identify the primary pathogen, as standard culture-based assays are prone to false positives in the case of polymicrobial infections, and false negatives due to limitations in sample acquisition and antibiotic use before presentation. To improve upon our current diagnostic methods for MSKI, we developed a multiplex immunoassay for antigen-specific IgGs in serum (Luminex), and medium enriched for newly synthesized antibodies (MENSA) for anti-S. aureus and GBS generated from cultured peripheral blood mononuclear cells (PBMCs) of orthopedic infection patients undergoing surgical treatment. Samples were obtained from 110 MSKI patients: 80 diabetic foot ulcer, 21 periprosthetic joint infection, 5 septic arthritis, 2 spine, 1 hand, and 1 fracture-related infection (FRI). Anti-S. aureus and anti-GBS antibody titers were compared to culture results to assess their concordance in identifying the pathogens. Immunoassay, particularly MENSA, showed high diagnostic potential for monomicrobial S. aureus and GBS orthopedic infections (AUC > 0.95). MENSA also demonstrated diagnostic potential for GBS polymicrobial orthopedic infection and for GBS DFU (AUC > 0.83 for both). Serum showed high diagnostic potential for S. aureus PJI (AUC > 0.95). Taken together, these findings support the development of species-specific immunoassays for the identification of causal pathogens in active MSKI, especially in conjunction with standard culture.
金黄色葡萄球菌和无乳链球菌(B 组链球菌,GBS)是深部肌肉骨骼感染(MSKI)的常见病因,给患者带来严重的发病率,并给医疗保健系统带来巨大的成本。MSKI 的主要挑战之一是缺乏准确识别主要病原体的可靠诊断方法,因为标准的基于培养的检测方法在混合感染的情况下容易出现假阳性,并且由于在出现之前的样本采集和抗生素使用限制,也容易出现假阴性。为了改进我们目前用于 MSKI 的诊断方法,我们开发了一种用于血清中抗原特异性 IgG 的多重免疫分析(Luminex),以及用于从接受手术治疗的骨科感染患者培养的外周血单核细胞(PBMCs)中产生的针对金黄色葡萄球菌和 GBS 的新合成抗体的培养基富集(MENSA)。从 110 名 MSKI 患者中获得了样本:80 名糖尿病足溃疡,21 名人工关节假体周围感染,5 名化脓性关节炎,2 名脊柱感染,1 名手部感染和 1 名骨折相关感染(FRI)。将抗金黄色葡萄球菌和抗 GBS 抗体滴度与培养结果进行比较,以评估它们在识别病原体方面的一致性。免疫分析,特别是 MENSA,显示出对单一致病菌金黄色葡萄球菌和 GBS 骨科感染具有很高的诊断潜力(AUC>0.95)。MENSA 还显示出对 GBS 混合感染骨科感染和 GBS DFU 的诊断潜力(两者的 AUC>0.83)。血清对金黄色葡萄球菌 PJI 具有很高的诊断潜力(AUC>0.95)。综上所述,这些发现支持开发用于识别活跃性 MSKI 中因果病原体的特异性免疫分析方法,尤其是与标准培养方法结合使用。