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首页> 外文期刊>Brazilian Journal of Medical and Biological Research >The Shiga toxin 2 B subunit inhibits net fluid absorption in human colon and elicits fluid accumulation in rat colon loops
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The Shiga toxin 2 B subunit inhibits net fluid absorption in human colon and elicits fluid accumulation in rat colon loops

机译:志贺毒素2 B亚基抑制人类结肠中的净液体吸收并引起大鼠结肠环中的液体蓄积

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Shiga toxin (Stx)-producing Escherichia coli (STEC) colonizes the large intestine causing a spectrum of disorders, including watery diarrhea, bloody diarrhea (hemorrhagic colitis), and hemolytic-uremic syndrome. It is estimated that hemolytic-uremic syndrome is the most common cause of acute renal failure in infants in Argentina. Stx is a multimeric toxin composed of one A subunit and five B subunits. In this study we demonstrate that the Stx2 B subunit inhibits the water absorption (Jw) across the human and rat colonic mucosa without altering the electrical parameters measured as transepithelial potential difference and short circuit current. The time-course Jw inhibition by 400 ng/ml purified Stx2 B subunit was similar to that obtained using 12 ng/ml Stx2 holotoxin suggesting that both, A and B subunits of Stx2 contributed to inhibit the Jw. Moreover, non-hemorrhagic fluid accumulation was observed in rat colon loops after 16 h of treatment with 3 and 30 ng/ml Stx2 B subunit. These changes indicate that Stx2 B subunit induces fluid accumulation independently of A subunit activity by altering the usual balance of intestinal absorption and secretion toward net secretion. In conclusion, our results suggest that the Stx2 B subunit, which is non-toxic for Vero cells, may contribute to the watery diarrhea observed in STEC infection. Further studies will be necessary to determine whether the toxicity of Stx2 B subunit may have pathogenic consequences when it is used as a component in an acellular STEC vaccine or as a vector in cancer vaccines.
机译:产生志贺毒素(Stx)的大肠杆菌(STEC)移居大肠,引起一系列疾病,包括水样腹泻,血性腹泻(出血性结肠炎)和溶血尿毒症候群。据估计,溶血尿毒综合征是阿根廷婴儿急性肾衰竭的最常见原因。 Stx是由一个A亚基和五个B亚基组成的多聚体毒素。在这项研究中,我们证明了Stx2 B亚基抑制了人类和大鼠结肠粘膜的吸水率(Jw),而没有改变经上皮电位差和短路电流所测得的电参数。 400 ng / ml纯化的Stx2 B亚基对时程Jw的抑制作用类似于使用12 ng / ml Stx2全息毒素获得的Jw抑制作用,表明Stx2的A和B亚基均有助于抑制Jw。此外,在用3 ng / ml和30 ng / ml Stx2 B亚单位处理16小时后,在大鼠结肠环中观察到了非出血性液体积聚。这些变化表明,Stx2 B亚基通过改变肠道吸收和向净分泌的分泌的通常平衡而独立于A亚基活性诱导液体蓄积。总之,我们的结果表明,对Vero细胞无毒的Stx2 B亚基可能会导致STEC感染中出现的水样腹泻。当Stx2 B亚基用作无细胞STEC疫苗的组成部分或用作癌症疫苗的载体时,有必要进行进一步的研究以确定Stx2 B亚基的毒性是否具有致病性。

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