| Literature DB >> 29178668 |
Hannah Trøstrup1, Christian J Lerche1, Lars J Christophersen1, Kim Thomsen1, Peter Ø Jensen1, Hans Petter Hougen2, Niels Høiby1,3, Claus Moser1.
Abstract
Biofilm-infected wounds are clinically challenging. Vascular endothelial growth factor and host defence S100A8/A9 are crucial for wound healing but may be suppressed by biofilms. The natural course of Pseudomonas aeruginosa biofilm infection was compared in central and peripheral zones of burn-wounded, infection-susceptible BALB/c mice, which display delayed wound closure compared to C3H/HeN mice. Wounds were evaluated histopathologically 4, 7 or 10 days post-infection. Photoplanimetry evaluated necrotic areas. P. aeruginosa biofilm suppressed vascular endothelial growth factor levels centrally in BALB/c wounds but increased peripheral levels 4-7 days post-infection. Central zones of the burn wound displayed lower levels of central vascular endothelial growth factor as observed 4 and 7 days post-infection in BALB/c mice compared to their C3H/HeN counterparts. Biofilm suppressed early, centrally located S100A8/A9 in BALB/c and centrally and peripherally later on in C3H/HeN wounds as compared to uninfected mice. Peripheral polymorphonuclear-dominated inflammation and larger necrosis were observed in BALB/c wounds. In conclusion, P. aeruginosa biofilm modulates wounds by suppressing central, but inducing peripheral, vascular endothelial growth factor levels and reducing host response in wounds of BALB/c mice. This suppression is detrimental to the resolution of biofilm-infected necrosis.Entities:
Keywords: Chronic wounds; Pseudomonas aeruginosa biofilm infection; S100A8/A9; Vascular endothelial growth factor; Wound necrosis
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Year: 2017 PMID: 29178668 PMCID: PMC7949748 DOI: 10.1111/iwj.12846
Source DB: PubMed Journal: Int Wound J ISSN: 1742-4801 Impact factor: 3.315