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首页> 外文期刊>Infection and immunity >Simultaneous Exposure to Escherichia coli Heat-Labile and Heat-Stable Enterotoxins Increases Fluid Secretion and Alters Cyclic Nucleotide and Cytokine Production by Intestinal Epithelial Cells
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Simultaneous Exposure to Escherichia coli Heat-Labile and Heat-Stable Enterotoxins Increases Fluid Secretion and Alters Cyclic Nucleotide and Cytokine Production by Intestinal Epithelial Cells

机译:同时暴露于大肠杆菌的热不稳定和热稳定肠毒素会增加液体分泌,并改变肠道上皮细胞产生的环核苷酸和细胞因子

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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.
机译:肠毒素性大肠杆菌(ETEC)是腹泻病和死亡的重要原因,尤其是在发展中国家的儿童中。 ETEC通过在小肠中定殖并产生热不稳定毒素(LT),热稳定毒素(ST)或LT和ST(LT + ST)两者而引起疾病。大多数ETEC菌株均产生ST和LT。尽管生产LT + ST的生物很普遍,但很少有研究检查同时暴露于这两种有效肠毒素的生理或免疫后果。在本报告中,我们证明当同时存在LT和ST时,它们会增加水向肠道内腔的运动速度,超过单独使用任何一种毒素所观察到的水平。如所期望的,当用ST处理时,培养的肠上皮细胞增加其细胞内环GMP(cGMP)的表达,而当用LT处理时,其细胞内环AMP(cAMP)的表达增加。当两种毒素都存在时,与相应的单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着降低。这些发现表明,与仅表达LT或ST的菌株相比,表达LT + ST的ETEC菌株诱导的上皮细胞中毒与分泌结果可能存在复杂的差异。我们的研究结果还揭示了一种新的机制,其中ST产生可能会降低宿主对感染生物体发起有效的先天或适应性免疫应答的能力。

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