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Rat Burn Model to Study Full-Thickness Cutaneous Thermal Burn and Infection
Published on: August 23, 2022
Development of Pseudomonas aeruginosa Biofilms in Partial-Thickness Burn Wounds Using a Sprague-Dawley Rat Model
Kenneth S Brandenburg1, Alan J Weaver1, Liwu Qian1
1Dental and Craniofacial Trauma Research and Tissue Regeneration Directorate (DCTRTRD), U.S. Army Institute of Surgical Research (USAISR), JBSA-Fort Sam Houston, San Antonio, Texas.
Abstract:
We used a modified Walker-Mason scald burn rat model to demonstrate that Pseudomonas aeruginosa, a common opportunistic pathogen in the burn ward and notable biofilm former, establishes biofilms within deep partial-thickness burn wounds in rats.Deep partial-thickness burn wounds, ~10% of the TBSA, were created in anesthetized male Sprague-Dawley rats (350-450 g; n = 84). Immediately post-burn, 100 µl of P. aeruginosa in phosphate-buffered saline at 1 × 103, 1 × 104, or 1 × 105 cells/wound was spread over the burn surface . At 1, 3, 7, and 11 days post-burn, animals were euthanized and blood and tissue were collected for complete blood counts, colony-forming unit (CFU) counts, biofilm gene expression, histology, scanning electron microscopy (SEM), and myeloperoxidase activity in the burn eschar.P. aeruginosa developed robust biofilm wound infections, plateauing at ~1 × 109 CFU/g burn tissue within 7 days regardless of inoculum size. Expression of Pseudomonas alginate genes and other virulence factors in the infected wound indicated formation of mature P. aeruginosa biofilm within the burn eschar. Compared to un-inoculated wounds, P. aeruginosa infection caused both local and systemic immune responses demonstrated by changes in systemic neutrophil counts, histology, and myeloperoxidase activity within the burn wound. Additionally, SEM showed P. aeruginosa enmeshed within an extracellular matrix on the burn surface as well as penetrating 500-600 µm deep into the eschar.P. aeruginosa establishes biofilms within deep partial-thickness burn wounds and invades deep into the burned tissue. This new in vivo biofilm infection model is valuable for testing novel anti-biofilm agents to advance burn care.
Insights
Pseudomonas aeruginosa forms robust biofilms in deep burn wounds, invading tissue and triggering immune responses. This new rat model aids in developing anti-biofilm treatments for burn care.
Area of Science:
- Microbiology
- Infectious Diseases
- Wound Healing
Background:
- Pseudomonas aeruginosa is a common opportunistic pathogen in burn units.
- Biofilm formation by P. aeruginosa complicates wound healing and treatment.
- Deep partial-thickness burn wounds provide a suitable environment for biofilm development.
Purpose of the Study:
- To establish and characterize a rat model of Pseudomonas aeruginosa biofilm infection in deep partial-thickness burn wounds.
- To investigate the development, gene expression, and host immune response to P. aeruginosa biofilms in vivo.
- To assess the depth of biofilm invasion within burn eschar.
Main Methods:
- A modified Walker-Mason scald burn model was used in Sprague-Dawley rats.
- Burn wounds were inoculated with varying concentrations of P. aeruginosa.
- Analysis included CFU counts, gene expression, histology, SEM, and myeloperoxidase activity.
Main Results:
- P. aeruginosa rapidly formed mature biofilms in burn wounds, reaching ~1 × 109 CFU/g tissue within 7 days.
- Biofilm formation was confirmed by alginate gene expression and SEM visualization of bacteria within the eschar.
- Infection induced local and systemic immune responses, including changes in neutrophil counts and myeloperoxidase activity.
Conclusions:
- Pseudomonas aeruginosa establishes robust biofilms within deep partial-thickness burn wounds in this in vivo model.
- The bacteria invade deeply into the burn eschar, forming a mature biofilm.
- This model is valuable for evaluating novel anti-biofilm therapies to improve burn wound management.
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