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Updated: Aug 27, 2025

Novel Diagnostics in Revision Arthroplasty: Implant Sonication and Multiplex Polymerase Chain Reaction
Published on: December 3, 2017
A 92 protein inflammation panel performed on sonicate fluid differentiates periprosthetic joint infection from
Cody R Fisher1,2, Harold I Salmons3, Jay Mandrekar2,4
1Department of Immunology, Mayo Clinic Graduate School of Biomedical Sciences, Mayo Clinic, Rochester, MN, USA.
Abstract:
Periprosthetic joint infection (PJI) is a major complication of total joint arthroplasty, typically necessitating surgical intervention and prolonged antimicrobial therapy. Currently, there is no perfect assay for PJI diagnosis. Proteomic profiling of sonicate fluid has the potential to differentiate PJI from non-infectious arthroplasty failure (NIAF) and possibly clinical subsets of PJI and/or NIAF. In this study, 200 sonicate fluid samples, including 90 from subjects with NIAF (23 aseptic loosening, 35 instability, 10 stiffness, five osteolysis, and 17 other) and 110 from subjects with PJI (40 Staphylococcus aureus, 40 Staphylococcus epidermidis, 10 Staphylococcus lugdunensis, 10 Streptococcus agalactiae, and 10 Enterococcus faecalis) were analyzed by proximity extension assay using the 92 protein Inflammation Panel from Olink Proteomics. Thirty-seven of the 92 proteins examined, including CCL20, OSM, EN-RAGE, IL8, and IL6, were differentially expressed in PJI versus NIAF sonicate fluid samples, with none of the 92 proteins differentially expressed between staphylococcal versus non-staphylococcal PJI, nor between the different types of NIAF studied. IL-17A and CCL11 were differentially expressed between PJI caused by different bacterial species, with IL-17A detected at higher levels in S. aureus compared to S. epidermidis and S. lugdunensis PJI, and CCL11 detected at higher levels in S. epidermidis compared to S. aureus and S. agalactiae PJI. Receiver operative characteristic curve analysis identified individual proteins and combinations of proteins that could differentiate PJI from NIAF. Overall, proteomic profiling using this small protein panel was able to differentiate between PJI and NIAF sonicate samples and provide a better understanding of the immune response during arthroplasty failure.
Insights
Proteomic profiling of sonicate fluid can differentiate periprosthetic joint infection (PJI) from non-infectious arthroplasty failure (NIAF). This study identified specific proteins that distinguish PJI, aiding in diagnosis and understanding infection mechanisms.
Area of Science:
- Biochemistry
- Immunology
- Orthopedic Surgery
Background:
- Periprosthetic joint infection (PJI) is a severe complication of total joint arthroplasty, often requiring revision surgery and long-term antibiotics.
- Current diagnostic methods for PJI lack perfection, highlighting the need for improved diagnostic assays.
- Proteomic analysis of sonicate fluid presents a promising avenue for distinguishing PJI from non-infectious arthroplasty failure (NIAF).
Purpose of the Study:
- To investigate the potential of proteomic profiling of sonicate fluid to differentiate PJI from NIAF.
- To identify specific protein biomarkers indicative of PJI and its subtypes.
- To explore the differences in protein expression related to various causative bacterial species in PJI.
Main Methods:
- Analysis of 200 sonicate fluid samples (110 PJI, 90 NIAF) using Olink Proteomics' 92-protein Inflammation Panel via proximity extension assay.
- Comparison of protein expression profiles between PJI and NIAF groups, as well as between different subtypes of PJI and NIAF.
- Receiver operative characteristic (ROC) curve analysis to assess the diagnostic accuracy of identified proteins and their combinations.
Main Results:
- Thirty-seven of 92 proteins showed differential expression between PJI and NIAF sonicate fluid.
- No significant protein expression differences were found between staphylococcal versus non-staphylococcal PJI or between different NIAF types.
- IL-17A and CCL11 levels differed between PJI caused by specific bacterial species (e.g., S. aureus vs. S. epidermidis).
Conclusions:
- Proteomic profiling of sonicate fluid is effective in differentiating PJI from NIAF.
- Specific protein biomarkers can aid in the diagnosis of PJI.
- This approach enhances understanding of the immune response in arthroplasty failure and infection.

