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Contamination of wounds with fecal bacteria in immuno-suppressed mice. | LitMetric

AI Article Synopsis

  • Immunocompromised patients often get chronic wounds, especially ulcers, which can become infected by multiple types of bacteria.
  • This study created a new mouse model that uses bacteria from fecal matter to better mimic real-life infections in people who are sick and can't move.
  • Researchers found that when the mice were treated to weaken their immune systems and infected with diluted fecal bacteria, their wound healing was significantly slower, helping to test new ideas for treating these infections.

Article Abstract

Immunocompromised patients are predisposed to chronically infected wounds. Especially ulcers in the dorsal region often experience secondary polymicrobial infections. However, current wound infection models mostly use single-strain bacteria. To mimic clinically occurring infections caused by fecal contamination in immunocompromised/immobile patients, which differ significantly from single-strain infections, the present study aimed at the establishment of a new mouse model using infection by fecal bacteria. Dorsal circular excision wounds in immunosuppressed mice were infected with fecal slurry solution in several dilutions up to 1:8,000. Impact of immunosuppressor, bacterial load and timing on development of wound infections was investigated. Wounds were analyzed by scoring, 3D imaging and swab analyses. Autofluorescence imaging was not successful. Dose-finding of cyclophosphamide-induced immunosuppression was necessary for establishment of bacterial wound infections. Infection with fecal slurry diluted 1:166 to 1:400 induced significantly delayed wound healing (p < 0.05) without systemic reactions. Swab analyses post-infection matched the initial polymicrobial suspension. The customized wound score confirmed significant differences between the groups (p < 0.05). Here we report the establishment of a simple, new mouse model for clinically occurring wound infections by fecal bacteria and the evaluation of appropriate wound analysis methods. In the future, this model will provide a suitable tool for the investigation of complex microbiological interactions and evaluation of new therapeutic approaches.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7359036PMC
http://dx.doi.org/10.1038/s41598-020-68323-5DOI Listing

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