Kreisberg Roderick B, Harper Jill, Strauman Maura C, Marohn Mark, Clements John D, Nataro James P
Division of Gastroenterology and Hepatology, Department of Medicine, University of Maryland School of Medicine, Baltimore, MD, USA.
Am J Trop Med Hyg. 2011 Mar;84(3):451-5. doi: 10.4269/ajtmh.2011.10-0445.
Enterotoxigenic Escherichia coli (ETEC) is a common cause of acute diarrhea in resource-poor settings. We report that some ETEC strains elicit a reduction in trans-epithelial electrical resistance (TER) in polarized T84 epithelial cell monolayers. The effect was irreversible up to 48 hours after a three-hour infection and was observed with heat-labile enterotoxin (LT)-producing strains, but not with heat-stable enterotoxin (ST)-producing strains. Using purified LT, a mutant with reduced ADP-ribosylating activity, and the LT-B subunit alone, we demonstrate that TER reduction requires a functional enterotoxin. Treatment of monolayers with LT or LT-producing strains of ETEC increases paracellular permeability to fluorescein isothiocyanate-dextran. Our data suggest that LT-producing ETEC strains may induce intestinal barrier dysfunction.
产肠毒素大肠杆菌(ETEC)是资源匮乏地区急性腹泻的常见病因。我们报告称,一些ETEC菌株会导致极化的T84上皮细胞单层的跨上皮电阻(TER)降低。在三小时感染后的48小时内,这种影响是不可逆的,并且在产不耐热肠毒素(LT)的菌株中观察到了这种现象,但在产耐热肠毒素(ST)的菌株中未观察到。使用纯化的LT、具有降低的ADP - 核糖基化活性的突变体以及单独的LT - B亚基,我们证明TER降低需要功能性肠毒素。用LT或产LT的ETEC菌株处理单层细胞会增加细胞旁对异硫氰酸荧光素 - 葡聚糖的通透性。我们的数据表明,产LT的ETEC菌株可能会诱导肠道屏障功能障碍。