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Injury and mechanism of recombinant E. coli expressing STaon piglets colon

机译:表达STa的重组大肠杆菌的损伤及其机制在仔猪结肠上

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摘要

Enterotoxigenic Escherichia coli (ETEC) is primary pathogenic bacteria of piglet diarrhea, over two thirds of piglets diarrhea caused by ETEC are resulted from STa-producing ETEC strains. This experiment was conducted to construct the recombinant E. coli expressing STa and study the injury and mechanism of recombinant E. coli expressing STa on 7 days old piglets colon. Twenty-four 7 days old piglets were allotted to four treatments: control group, STa group (2 × 109 CFU E. coli LMG194-STa), LMG194 group (2 × 109 CFU E. coli LMG194) and K88 group (2 × 109 CFU E. coli K88). The result showed that E. coli infection significantly increased diarrhea rates; changed DAO activity in plasma and colon; damaged colonic mucosal morphology including crypt depth, number of globet cells, density of lymphocytes and lamina propria cell density; substantially reduced antioxidant capacity by altering activities of GSH-Px, SOD, and TNOS and productions of MDA and H2O2; obviously decreased AQP3, AQP4 and KCNJ13 protein expression levels; substantially altered the gene expression levels of inflammatory cytokines. Conclusively, STa group had the biggest effect on these indices in four treatment groups. These results suggested that the recombinant strain expressed STa can induce pigletsdiarrhea and colonic morphological and funtional damage by altering expression of proteinsconnect to transportation function and genes associated with intestinal injury andinflammatory cytokines.
机译:肠毒素性大肠杆菌(ETEC)是仔猪腹泻的主要致病菌,由ETEC引起的仔猪腹泻的三分之二以上是由产生STa的ETEC菌株引起的。进行了该实验以构建表达STa的重组大肠杆菌,并研究了表达STa的重组大肠杆菌对7日龄仔猪结肠的损伤及其机制。将24只7天大的仔猪分配给四种治疗方法:对照组,STa组(2×10 9 CFU大肠杆菌LMG194-STa),LMG194组(2×10 9 < / sup> CFU大肠杆菌LMG194)和K88组(2×10 9 CFU大肠杆菌K88)。结果表明,大肠杆菌感染显着增加了腹泻率。改变血浆和结肠中的DAO活性;受损的结肠粘膜形态,包括隐窝深度,地球细胞数量,淋巴细胞密度和固有层细胞密度;通过改变GSH-Px,SOD和TNOS的活性以及MDA和H2O2的产生,大大降低了抗氧化能力; AQP3,AQP4和KCNJ13蛋白表达水平明显降低;实质上改变了炎症细胞因子的基因表达水平。结论是,在四个治疗组中,STa组对这些指标的影响最大。这些结果表明,表达STa的重组菌株可以诱导仔猪腹泻和结肠形态和功能损伤,通过改变蛋白质表达与运输功能和与肠损伤相关的基因有关炎性细胞因子。

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