Monoclonal Antibody Disrupts Biofilm Structure and Restores Antibiotic Susceptibility in an Orthopedic Implant Infection Model
Authors:
- Zachary D. C. BurkeZBZachary D. C. Burke
- Christopher M. HartCHChristopher M. Hart
- Benjamin V. KelleyBKBenjamin V. Kelley
- Zeinab MamoueiZMZeinab Mamouei
- Gideon W. BlumsteinGBGideon W. Blumstein
- Christopher HamadCHChristopher Hamad
- Kellyn HoriKHKellyn Hori
- Nicolas CevallosNCNicolas Cevallos
- Christina VillalpandoCVChristina Villalpando
- Nicole TruongNTNicole Truong
- Amr TurkmaniATAmr Turkmani
- Micah RalstonMRMicah Ralston
Open Access
- 28 September 2023
- journal article
- research article
- Published by MDPI AG in Antibiotics
- Vol. 12 (10) , 1490
Abstract
Bacterial biofilms on orthopedic implants are resistant to the host immune response and to traditional systemic antibiotics. Novel therapies are needed to improve patient outcomes. TRL1068 is a human monoclonal antibody (mAb) against a biofilm anchoring protein. For assessment of this agent in an orthopedic implant infection model, efficacy was measured by reduction in bacterial burden of Staphylococcus aureus, the most common pathogen for prosthetic joint infections (PJI). Systemic treatment with the biofilm disrupting mAb TRL1068 in conjunction with vancomycin eradicated S. aureus from steel pins implanted in the spine for 26 of 27 mice, significantly more than for vancomycin alone. The mechanism of action was elucidated by two microscopy studies. First, TRL1068 was localized to biofilm using a fluorescent antibody tag. Second, a qualitative effect on biofilm structure was observed using scanning electron microscopy (SEM) to examine steel pins that had been treated in vivo. SEM images of implants retrieved from control mice showed abundant three-dimensional biofilms, whereas those from mice treated with TRL1068 did not. Clinical Significance: TRL1068 binds at high affinity to S. aureus biofilms, thereby disrupting the three-dimensional structure and significantly reducing implant CFUs in a well-characterized orthopedic model for which prior tested agents have shown only partial efficacy. TRL1068 represents a promising systemic treatment for orthopedic implant infection.Keywords
Funding Information
- National Institute of Arthritis and Musculoskeletal and Skin Diseases (5K08AR069112-01, T32AR059033, R44AI150143)
- National Institute of Allergy and Infectious Diseases (5K08AR069112-01, T32AR059033, R44AI150143)
This publication has 37 references indexed in Scilit:
- From in vitro to in vivo Models of Bacterial Biofilm-Related InfectionsPathogens, 2013
- Systemic Antibiotic Therapy for Chronic Osteomyelitis in AdultsClinical Infectious Diseases, 2011
- Molecular Imaging and Contrast Agent Database (MICAD): Evolution and ProgressMolecular Imaging and Biology, 2011
- Mouse model of chronic post‐arthroplasty infection: Noninvasive in vivo bioluminescence imaging to monitor bacterial burden for long‐term studyJournal of Orthopaedic Research, 2011
- Proteomic Analyses of Nucleoid-Associated Proteins in Escherichia coli, Pseudomonas aeruginosa, Bacillus subtilis, and Staphylococcus aureusPLOS ONE, 2011
- A Mouse Model of Post-Arthroplasty Staphylococcus aureus Joint Infection to Evaluate In Vivo the Efficacy of Antimicrobial Implant CoatingsPLOS ONE, 2010
- Revision Hip Arthroplasty: Infection is the Most Common Cause of FailureClinical Orthopaedics and Related Research, 2010
- The Epidemiology of Revision Total Knee Arthroplasty in the United StatesClinical Orthopaedics and Related Research, 2010
- Projections of Primary and Revision Hip and Knee Arthroplasty in the United States from 2005 to 2030Journal of Bone and Joint Surgery, 2007
- Monitoring BioluminescentStaphylococcus aureusInfections in Living Mice Using a NovelluxABCDEConstructInfection and Immunity, 2000