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铜绿假单胞菌生物膜通过抑制血管上皮生长因子阻碍小鼠中央伤口愈合。

Pseudomonas aeruginosa biofilm hampers murine central wound healing by suppression of vascular epithelial growth factor.

机构信息

Department of Clinical Microbiology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.

Department of Forensic Medicine, University of Copenhagen, Copenhagen, Denmark.

出版信息

Int Wound J. 2018 Feb;15(1):123-132. doi: 10.1111/iwj.12846. Epub 2017 Nov 27.

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.

摘要

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。

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