Departments of Medicine and Physiology/Biophysics, University of California, School of Medicine, Irvine, California and Medical Research Service, Veterans Affairs Medical Center, Long Beach, California; and.
Am J Physiol Cell Physiol. 2013 Dec 1;305(11):C1185-91. doi: 10.1152/ajpcell.00276.2013. Epub 2013 Oct 16.
Infections with enteric pathogens like enterotoxigenic Escherichia coli (ETEC) is a major health issue worldwide and while diarrhea is the major problem, prolonged, severe, and dual infections with multiple pathogens may also compromise the nutritional status of the infected individuals. There is almost nothing currently known about the effect of ETEC infection on intestinal absorptions of water-soluble vitamins including thiamin. We examined the effect of ETEC infection on intestinal uptake of the thiamin using as a model the human-derived intestinal epithelial Caco-2 cells. The results showed that infecting confluent Caco-2 monolayers with live ETEC (but not with boiled/killed ETEC or nonpathogenic E. coli) or treatment with bacterial culture supernatant led to a significant inhibition in thiamin uptake. This inhibition appears to be caused by a heat-labile and -secreted ETEC component and is mediated via activation of the epithelial adenylate cyclase system. The inhibition in thiamin uptake by ETEC was associated with a significant reduction in expression of human thiamin transporter-1 and -2 (hTHTR1 and hTHTR2) at the protein and mRNA levels as well as in the activity of the SLC19A2 and SLC19A3 promoters. Dual infection of Caco-2 cells with ETEC and EPEC (enteropathogenic E. coli) led to compounded inhibition in intestinal thiamin uptake. These results show for the first time that infection of human intestinal epithelial cells with ETEC causes a significant inhibition in intestinal thiamin uptake. This inhibition is mediated by a secreted heat-labile toxin and is associated with a decrease in the expression of intestinal thiamin transporters.
肠致病性病原体(如肠毒素性大肠杆菌,ETEC)感染是一个全球性的重大健康问题,虽然腹泻是主要问题,但长期、严重和多重病原体的双重感染也可能损害受感染个体的营养状况。目前几乎没有关于 ETEC 感染对包括硫胺素在内的水溶性维生素肠道吸收的影响的任何信息。我们使用人源肠上皮 Caco-2 细胞作为模型,研究了 ETEC 感染对肠道摄取硫胺素的影响。结果表明,用活 ETEC(而非煮沸/灭活 ETEC 或非致病性大肠杆菌)感染融合的 Caco-2 单层细胞,或用细菌培养上清液处理,均可显著抑制硫胺素摄取。这种抑制似乎是由一种不耐热和分泌的 ETEC 成分引起的,通过激活上皮细胞环腺苷酸系统来介导。ETEC 对硫胺素摄取的抑制与人类硫胺素转运蛋白-1 和 -2(hTHTR1 和 hTHTR2)在蛋白质和 mRNA 水平以及 SLC19A2 和 SLC19A3 启动子活性的显著减少有关。Caco-2 细胞与 ETEC 和 EPEC(肠致病性大肠杆菌)的双重感染导致肠道硫胺素摄取的抑制作用进一步加剧。这些结果首次表明,人肠上皮细胞感染 ETEC 会导致肠道硫胺素摄取显著抑制。这种抑制是由一种分泌的热不稳定毒素介导的,并与肠道硫胺素转运蛋白表达减少有关。