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DOI 10.1242/dmm.045385

Медицинская библиотека · Disease models & mechanisms · 2020

Rabbit model of Staphylococcus aureus implant-associated spinal infection.

Gordon Oren, Miller Robert J, Thompson John M, Ordonez Alvaro A, Klunk Mariah H, Dikeman Dustin A, Joyce Daniel P, Ruiz-Bedoya Camilo A, Miller Lloyd S, Jain Sanjay K

СтатьяПоддержка NIH: внешняя программаПеревод в очереди

Аннотация

Post-surgical implant-associated spinal infection is a devastating complication commonly caused by Staphylococcus aureus Biofilm formation is thought to reduce penetration of antibiotics and immune cells, contributing to chronic and difficult-to-treat infections. A rabbit model of a posterior-approach spinal surgery was created, in which bilateral titanium pedicle screws were interconnected by a plate at the level of lumbar vertebra L6 and inoculated with a methicillin-resistant S.aureus (MRSA) bioluminescent strain. In vivo whole-animal bioluminescence imaging (BLI) and ex vivo bacterial cultures demonstrated a peak in bacterial burden by day 14, when wound dehiscence occurred. Structures suggestive of biofilm, visualized by scanning electron microscopy, were evident up to 56 days following infection. Infection-induced inflammation and bone remodeling were also monitored using 18F-fluorodeoxyglucose (18F-FDG) positron emission tomography (PET) and computed tomography (CT). PET imaging signals were noted in the soft tissue and bone surrounding the implanted materials. CT imaging demonstrated marked bone remodeling and a decrease in dense bone at the infection sites. This rabbit model of implant-associated spinal infection provides a valuable preclinical in vivo approach to investigate the pathogenesis of implant-associated spinal infections and to evaluate novel therapeutics.

Для цитирования: Gordon Oren, Miller Robert J, Thompson John M, Ordonez Alvaro A, Klunk Mariah H, Dikeman Dustin A, Joyce Daniel P, Ruiz-Bedoya Camilo A, Miller Lloyd S, Jain Sanjay K. Rabbit model of Staphylococcus aureus implant-associated spinal infection.. Disease models & mechanisms. 2020. DOI: 10.1242/dmm.045385.

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