Distinct vasculotropic versus osteotropic features of S. agalactiae versus S. aureus implant-associated bone

Elysia A Masters1,2, Stephanie P Hao1, H Mark Kenney1,3

  • 1Center for Musculoskeletal Research, University of Rochester Medical Center, Rochester, New York, USA.

Insights

This study developed the first animal model for Group B Streptococcus (GBS) osteomyelitis, revealing its distinct vasculotropic infection pattern compared to Staphylococcus aureus bone infections.

Area of Science:

  • Orthopaedic Surgery
  • Infectious Diseases
  • Microbiology

Background:

  • Osteomyelitis is a severe complication of orthopaedic surgery, often caused by Staphylococcus aureus (S. aureus) or Group B Streptococcus (GBS, S. agalactiae).
  • S. aureus infections typically cause local bone destruction and implant loosening, while GBS infections often lead to systemic spread.
  • Existing animal models effectively study S. aureus osteomyelitis, but models for GBS osteomyelitis are lacking.

Purpose of the Study:

  • To establish and characterize the first quantitative animal model for S. agalactiae osteomyelitis.
  • To compare the pathogenic mechanisms and tissue tropism of S. aureus and S. agalactiae in implant-associated osteomyelitis.
  • To elucidate the distinct modes of bone colonization by these two bacterial species.

Main Methods:

  • Comparison of S. aureus and S. agalactiae in a murine model of implant-associated osteomyelitis.
  • In vitro analysis using scanning electron microscopy and CFU quantification for bacterial inocula.
  • In vivo assessment including body weight, CFU counts, X-ray, micro-CT, histology, and transmission electron microscopy.

Main Results:

  • S. aureus exhibited greater virulence than S. agalactiae, with more severe osteolysis and implant loosening.
  • S. agalactiae infections resulted in less bone destruction and fewer osteoclasts compared to S. aureus.
  • Transmission electron microscopy revealed S. agalactiae colonizes blood vessels (vasculotropic), while S. aureus colonizes the osteocyte network (osteotropic).

Conclusions:

  • This study successfully established the first quantitative animal model for S. agalactiae osteomyelitis.
  • S. agalactiae demonstrates a vasculotropic infection strategy in bone, distinct from the osteotropic strategy of S. aureus.
  • Understanding these distinct pathogenic behaviors is crucial for developing targeted treatments for different types of osteomyelitis.

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