A novel mouse model of soft-tissue infection using bioluminescence imaging allows noninvasive, real-time monitoring of bacterial growth

PLoS One. 2014 Sep 3;9(9):e106367. doi: 10.1371/journal.pone.0106367. eCollection 2014.

Abstract

Musculoskeletal infections, including surgical-site and implant-associated infections, often cause progressive inflammation and destroy areas of the soft tissue. Treating infections, especially those caused by multi-antibiotic resistant bacteria such as methicillin-resistant Staphylococcus aureus (MRSA) remains a challenge. Although there are a few animal models that enable the quantitative evaluation of infection in soft tissues, these models are not always reproducible or sustainable. Here, we successfully established a real-time, in vivo, quantitative mouse model of soft-tissue infection in the superficial gluteus muscle (SGM) using bioluminescence imaging. A bioluminescent strain of MRSA was inoculated into the SGM of BALB/c adult male mice, followed by sequential measurement of bacterial photon intensity and serological and histological analyses of the mice. The mean photon intensity in the mice peaked immediately after inoculation and remained stable until day 28. The serum levels of interleukin-6, interleukin-1 and C-reactive protein at 12 hours after inoculation were significantly higher than those prior to inoculation, and the C-reactive protein remained significantly elevated until day 21. Histological analyses showed marked neutrophil infiltration and abscesses containing necrotic and fibrous tissues in the SGM. With this SGM mouse model, we successfully visualized and quantified stable bacterial growth over an extended period of time with bioluminescence imaging, which allowed us to monitor the process of infection without euthanizing the experimental animals. This model is applicable to in vivo evaluations of the long-term efficacy of novel antibiotics or antibacterial implants.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Diagnostic Imaging
  • Disease Models, Animal
  • Luminescent Measurements
  • Methicillin-Resistant Staphylococcus aureus / growth & development
  • Methicillin-Resistant Staphylococcus aureus / isolation & purification*
  • Methicillin-Resistant Staphylococcus aureus / pathogenicity
  • Mice
  • Mice, Inbred BALB C
  • Soft Tissue Infections / diagnosis*
  • Soft Tissue Infections / microbiology
  • Soft Tissue Infections / pathology
  • Staphylococcal Infections / diagnosis*
  • Staphylococcal Infections / microbiology
  • Staphylococcal Infections / pathology
  • Staphylococcus aureus / growth & development
  • Staphylococcus aureus / isolation & purification*
  • Staphylococcus aureus / pathogenicity

Grants and funding

This work was supported by scientific research fund of Ministry of Education and Science, Kanagawa Academy of Science and Technology (KAST), a medical research grant on traffic accident from The General Insurance Association of Japan, Private Universities Foundation for the Development of Fundamental Research Strategies, Development of Next-generation Regenerative Medicine Process Using Biomaterials with Life Function on the Basis of Vertical Integration System, Keio Gijuku Academic Development Funds, and Research for Promoting Technological Seeds. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.