Deciphering the mechanism of action of Escherichia coli STb toxin using intestinal epithelial cells

利用肠上皮细胞破译大肠杆菌 STb 毒素的作用机制

• 批准号: 139070-2013
• 负责人: Dubreuil, Daniel
• 金额: $ 1.82万
• 依托单位: Université de Montréal
• 依托单位国家: 加拿大
• 项目类别: Discovery Grants Program - Individual
• 财政年份: 2013
• 资助国家: 加拿大
• 起止时间: 2013-01-01 至 2014-12-31
• 项目状态: 已结题
• 来源: https://www.nserc-crsng.gc.ca/ase-oro/Details-Detailles_eng.asp?id=522486
• 关键词: Deciphering; mechanism; action; Escherichia; coli

Enterotoxigenic Escherichia coli (ETEC) is responsible for major economic losses in animal production resulting from diarrhea. ETEC strains produce disease through attachment to host cells via colonization factors and then elaborate one or more type of enterotoxins that can act on the intestinal tissue. STb is one of the small molecular weight heat-stable toxins produced by ETEC. This virulence factor is now recognized as a major player in neonatal and post-weaning diarrhea in pigs. Although there have been many studies on STb, little comprehensive information is available on its mechanism of action compared to other enterotoxins produced by ETEC (such as LT and STa). It was shown that STb has to be internalized into a target cell to express toxicity. However, the internalization route of STb remains unknown. STb is classified as a cytotonic toxin; currently the accepted dogma to explain the secretion observed is that ion channels, in particular chloride, are stimulated together with an inhibition of sodium ions leading to an osmotic loss of water. Also, ion and water fluxes between epithelial cells are regulated by structures called tight junctions that seal the space between them. Preliminary data demonstrated that STb, as was shown also for other bacterial toxins, could act on TJs by opening these structures and permitting a loss of fluid. The goal of the research program is to study further the STb internalization pathway and TJ opening. We aim to decipher the mechanism of action of STb toxin. Fundamental understanding of the mechanism of action of this clinically important enterotoxin has potential for the development of preventive and/or therapeutic strategies to control STb-induced diarrheal disease.

产肠毒素大肠杆菌(ETEC)是腹泻给畜牧业生产造成的重大经济损失之一。ETEC菌株通过定植因子附着到宿主细胞上而产生疾病，然后阐述一种或多种可作用于肠道组织的肠毒素。STB是ETEC生产的一种小分子热稳定性毒素。这种毒力因子现在被认为是导致猪新生儿和断奶后腹泻的主要因素。虽然已经有很多关于STB的研究，但与ETEC产生的其他肠毒素(如LT和STA)相比，关于其作用机制的全面信息很少。研究表明，STB必须内化到靶细胞中才能表达毒性。然而，STB的内化途径仍不清楚。STB被归类为一种细胞毒性毒素；目前公认的解释所观察到的分泌的教义是离子通道，特别是氯化物，与钠离子的抑制一起被刺激，导致水分的渗透损失。此外，上皮细胞之间的离子和水的流动受到称为紧密连接的结构的调节，紧密连接封闭了它们之间的空间。初步数据表明，与其他细菌毒素一样，STB可以通过打开这些结构并允许液体损失来作用于TJ。该研究计划的目标是进一步研究STB的内化途径和TJ开放。我们的目标是破译STB毒素的作用机制。对这种临床上重要的肠毒素作用机制的基本了解对于制定预防和/或治疗策略以控制STB引起的腹泻疾病具有潜在的意义。