Department of Clinical Microbiology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.
Department of Forensic Medicine, University of Copenhagen, Copenhagen, Denmark.
Int Wound J. 2018 Feb;15(1):123-132. doi: 10.1111/iwj.12846. Epub 2017 Nov 27.
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.
生物膜感染的伤口具有临床挑战性。血管内皮生长因子和宿主防御 S100A8/A9 对伤口愈合至关重要,但可能被生物膜抑制。本研究比较了易感染烧伤的 BALB/c 小鼠和 C3H/HeN 小鼠烧伤创面中心区和周边区铜绿假单胞菌生物膜感染的自然病程,与 C3H/HeN 小鼠相比,BALB/c 小鼠的创面愈合延迟。感染后 4、7 或 10 天对创面进行组织病理学评估。光测法评估坏死面积。铜绿假单胞菌生物膜在 BALB/c 创面中心区抑制血管内皮生长因子水平,但在感染后 4-7 天增加外周水平。与 C3H/HeN 相比,感染后 4 和 7 天 BALB/c 创面中央区血管内皮生长因子水平较低。与未感染小鼠相比,生物膜抑制了 BALB/c 创面中早期、中央 S100A8/A9,而在 C3H/HeN 创面中晚期抑制中央和外周 S100A8/A9。BALB/c 创面中观察到外周多形核粒细胞为主的炎症和更大的坏死。结论:铜绿假单胞菌生物膜通过抑制中央、诱导外周血管内皮生长因子水平,并降低 BALB/c 小鼠创面的宿主反应来调节创面。这种抑制不利于生物膜感染性坏死的消退。