Read Lisa T, Hahn Rachel W, Thompson Carli C, Bauer David L, Norton Elizabeth B, Clements John D
Department of Microbiology and Immunology, Tulane University School of Medicine, New Orleans, Louisiana, USA.
Department of Microbiology and Immunology, Tulane University School of Medicine, New Orleans, Louisiana, USA
Infect Immun. 2014 Dec;82(12):5308-16. doi: 10.1128/IAI.02496-14. Epub 2014 Oct 6.
Enterotoxigenic Escherichia coli (ETEC) is a significant cause of diarrheal disease and death, especially in children in developing countries. ETEC causes disease by colonizing the small intestine and producing heat-labile toxin (LT), heat-stable toxin (ST), or both LT and ST (LT+ST). The majority of ETEC strains produce both ST and LT. Despite the prevalence of LT+ST-producing organisms, few studies have examined the physiologic or immunologic consequences of simultaneous exposure to these two potent enterotoxins. In the current report, we demonstrate that when LT and ST are both present, they increase water movement into the intestinal lumen over and above the levels observed with either toxin alone. As expected, cultured intestinal epithelial cells increased their expression of intracellular cyclic GMP (cGMP) when treated with ST and their expression of intracellular cyclic AMP (cAMP) when treated with LT. When both toxins were present, cGMP levels but not cAMP levels were synergistically elevated compared with the levels of expression caused by the corresponding single-toxin treatment. Our data also demonstrate that the levels of inflammatory cytokines produced by intestinal epithelial cells in response to LT are significantly reduced in animals exposed to both enterotoxins. These findings suggest that there may be complex differences between the epithelial cell intoxication and, potentially, secretory outcomes induced by ETEC strains expressing LT+ST compared with strains that express LT or ST only. Our results also reveal a novel mechanism wherein ST production may reduce the hosts' ability to mount an effective innate or adaptive immune response to infecting organisms.
产肠毒素大肠杆菌(ETEC)是导致腹泻病和死亡的一个重要原因,尤其是在发展中国家的儿童中。ETEC通过定殖于小肠并产生不耐热毒素(LT)、耐热毒素(ST)或同时产生LT和ST(LT+ST)来引发疾病。大多数ETEC菌株同时产生ST和LT。尽管产生LT+ST的菌株很普遍,但很少有研究探讨同时暴露于这两种强效肠毒素的生理或免疫后果。在本报告中,我们证明当LT和ST同时存在时,它们会使进入肠腔的水分移动比单独使用任何一种毒素时观察到的水平更高。正如预期的那样,培养的肠上皮细胞在用ST处理时细胞内环磷酸鸟苷(cGMP)的表达增加,在用LT处理时细胞内环磷酸腺苷(cAMP)的表达增加。当两种毒素都存在时,与相应单一毒素处理引起的表达水平相比,cGMP水平而非cAMP水平协同升高。我们的数据还表明,在同时暴露于两种肠毒素的动物中,肠上皮细胞对LT产生的炎性细胞因子水平显著降低。这些发现表明,与仅表达LT或ST的菌株相比,表达LT+ST的ETEC菌株在上皮细胞中毒以及潜在的分泌结果方面可能存在复杂差异。我们的结果还揭示了一种新机制,即ST的产生可能会降低宿主对感染生物体产生有效先天性或适应性免疫反应的能力。