Department of Surgery-Otorhinolaryngology Head and Neck Surgery, The Queen Elizabeth Hospital, University of Adelaide, Adelaide, SA, Australia.
Int Forum Allergy Rhinol. 2020 Jul;10(7):871-883. doi: 10.1002/alr.22566. Epub 2020 Jun 7.
Chronic rhinosinusitis patients (CRS) suffer from chronic inflammation of the sinus mucosa associated with chronic relapsing infections. Mucosal biofilms, associated with Staphylococcus aureus, have been implicated as a cause. We compared the effect of exoproteins secreted from clinical isolates of S aureus from CRS patients in planktonic and biofilm form on the nasal epithelial barrier.
Clinical S aureus isolates from 39 CRS patients were grown in planktonic and biofilm forms and their exoproteins concentrated. These were applied to primary human nasal epithelial cells grown at the air-liquid interface. Transepithelial electrical resistance, permeability of flourescein isothiocyanate-dextrans, and cytotoxicity were measured. Structure and expression of tight junctions zona occludens-1, and claudin-1 proteins were assessed by electron microscopy and immunofluorescence. The Wilcoxon signed rank test was used for statistical analyses.
S aureus biofilm exoproteins showed dose- and time-dependent reduction of transepithelial electrical resistance, increased cell toxicity, and increased permeability (p < 0.001) compared with equal concentrations of planktonic cultures. Discontinuity in zona occludens-1 and claudin-1 immunofluorescence was confirmed as disrupted tight junctions on electron microscopy.
S aureus biofilm exoproteins disrupt the mucosal barrier structure in a time- and dose-dependent manner and are toxic. Damage to the mucosal barrier by S aureus biofilm exoproteins may play a major role in CRS etiopathogenesis.
慢性鼻-鼻窦炎(CRS)患者的鼻窦黏膜存在慢性炎症,且与慢性复发性感染有关。金黄色葡萄球菌(S aureus)相关的黏膜生物膜被认为是其病因之一。我们比较了来自 CRS 患者的浮游和生物膜形式的临床分离 S aureus 分泌的外蛋白对鼻上皮屏障的影响。
将 39 例 CRS 患者的临床 S aureus 分离株在浮游和生物膜形式下培养,并浓缩其外蛋白。将这些外蛋白应用于在气液界面培养的原代人鼻上皮细胞。测量跨上皮电阻、荧光素异硫氰酸酯-葡聚糖的通透性和细胞毒性。通过电子显微镜和免疫荧光评估紧密连接蛋白封闭蛋白-1(zona occludens-1,ZO-1)和闭合蛋白-1(claudin-1)的结构和表达。使用 Wilcoxon 符号秩检验进行统计分析。
与等浓度的浮游培养物相比,S aureus 生物膜外蛋白表现出剂量和时间依赖性的跨上皮电阻降低、细胞毒性增加和通透性增加(p<0.001)。电子显微镜证实 ZO-1 和闭合蛋白-1 免疫荧光的不连续性为紧密连接的破坏。
S aureus 生物膜外蛋白以时间和剂量依赖的方式破坏黏膜屏障结构,并具有毒性。S aureus 生物膜外蛋白对黏膜屏障的损伤可能在 CRS 的发病机制中起主要作用。