Departamento de Bioquímica y Biología Molecular, Facultad de Ciencias Químicas y Farmacéuticas, Universidad de Chile, Correo 1, Santiago, Chile.
Microb Pathog. 2011 Nov;51(5):373-7. doi: 10.1016/j.micpath.2011.07.005. Epub 2011 Jul 18.
The cystic fibrosis transmembrane conductance regulator (CFTR) has been proposed as an epithelial cell receptor for the entry of Salmonella Typhi but not Salmonella Typhimurium. The bacterial ligand recognized by CFTR is thought to reside either in the S. Typhi lipopolysaccharide core region or in the type IV pili. Here, we assessed the ability of virulent strains of S. Typhi and S. Typhimurium to adhere to and invade BHK epithelial cells expressing either the wild-type CFTR protein or the ∆F508 CFTR mutant. Both S. Typhi and S. Typhimurium invaded the epithelial cells in a CFTR-independent fashion. Furthermore and also in a CFTR-independent manner, a S. Typhi pilS mutant adhered normally to BHK cells but displayed a 50% reduction in invasion as compared to wild-type bacteria. Immunofluorescence microscopy revealed that bacteria and CFTR do not colocalize at the epithelial cell surface. Together, our results strongly argue against the established dogma that CFTR is a receptor for entry of Salmonella to epithelial cells.
囊性纤维化跨膜电导调节因子 (CFTR) 被认为是肠上皮细胞摄取伤寒沙门氏菌而不是鼠伤寒沙门氏菌的受体。CFTR 识别的细菌配体被认为存在于伤寒沙门氏菌脂多糖核心区域或 IV 型菌毛中。在这里,我们评估了毒力菌株伤寒沙门氏菌和鼠伤寒沙门氏菌与表达野生型 CFTR 蛋白或 ∆F508 CFTR 突变体的 BHK 上皮细胞粘附和入侵的能力。伤寒沙门氏菌和鼠伤寒沙门氏菌均以 CFTR 非依赖性方式侵入上皮细胞。此外,以 CFTR 非依赖性方式,伤寒沙门氏菌 pilS 突变体正常粘附于 BHK 细胞,但与野生型细菌相比,入侵减少了 50%。免疫荧光显微镜显示细菌和 CFTR 不会在上皮细胞表面共定位。总之,我们的结果强烈反对 CFTR 是沙门氏菌进入上皮细胞的受体这一既定观点。