Swine Model of Biofilm Infection and Invisible Wounds

dc.contributor.authorEl Masry, Mohamed
dc.contributor.authorBhasme, Pramod
dc.contributor.authorMathew-Steiner, Shomita S.
dc.contributor.authorSmith, Jessica
dc.contributor.authorSmeenge, Thomas
dc.contributor.authorRoy, Sashwati
dc.contributor.authorSen, Chandan K.
dc.contributor.departmentSurgery, School of Medicine
dc.date.accessioned2024-09-05T11:06:14Z
dc.date.available2024-09-05T11:06:14Z
dc.date.issued2023-06-16
dc.description.abstractBiofilm infection is a major contributor to wound chronicity. The establishment of clinically relevant experimental wound biofilm infection requires the involvement of the host immune system. Iterative changes in the host and pathogen during the formation of such clinically relevant biofilm can only occur in vivo. The swine wound model is recognized for its advantages as a powerful pre-clinical model. There are several reported approaches for studying wound biofilms. In vitro and ex vivo systems are deficient in terms of the host immune response. Short-term in vivo studies involve acute responses and, thus, do not allow for biofilm maturation, as is known to occur clinically. The first long-term swine wound biofilm study was reported in 2014. The study recognized that biofilm-infected wounds may close as determined by planimetry, but the skin barrier function of the affected site may fail to be restored. Later, this observation was validated clinically. The concept of functional wound closure was thus born. Wounds closed but deficient in skin barrier function may be viewed as invisible wounds. In this work, we seek to report the methodological details necessary to reproduce the long-term swine model of biofilm-infected severe burn injury, which is clinically relevant and has translational value. This protocol provides detailed guidance on establishing an 8 week wound biofilm infection using P. aeruginosa (PA01). Eight full-thickness burn wounds were created symmetrically on the dorsum of domestic white pigs, which were inoculated with (PA01) at day 3 post-burn; subsequently, noninvasive assessments of the wound healing were conducted at different time points using laser speckle imaging (LSI), high-resolution ultrasound (HUSD), and transepidermal water loss (TEWL). The inoculated burn wounds were covered with a four-layer dressing. Biofilms, as established and confirmed structurally by SEM at day 7 post-inoculation, compromised the functional wound closure. Such an adverse outcome is subject to reversal in response to appropriate interventions.
dc.eprint.versionAuthor's manuscript
dc.identifier.citationEl Masry M, Bhasme P, Mathew-Steiner SS, et al. Swine Model of Biofilm Infection and Invisible Wounds. J Vis Exp. 2023;(196):10.3791/65301. Published 2023 Jun 16. doi:10.3791/65301
dc.identifier.urihttps://hdl.handle.net/1805/43150
dc.language.isoen_US
dc.publisherMyJove Corporation
dc.relation.isversionof10.3791/65301
dc.relation.journalJournal of Visualized Experiments
dc.rightsPublisher Policy
dc.sourcePMC
dc.subjectBandages
dc.subjectBiofilms
dc.subjectPseudomonas aeruginosa
dc.subjectSwine
dc.subjectWound healing
dc.subjectWound infection
dc.titleSwine Model of Biofilm Infection and Invisible Wounds
dc.typeArticle
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