Sha Jian, Kozlova E V, Chopra A K
Department of Microbiology and Immunology, The University of Texas Medical Branch, Galveston, Texas 77555-1070, USA.
Infect Immun. 2002 Apr;70(4):1924-35. doi: 10.1128/IAI.70.4.1924-1935.2002.
Three enterotoxins from the Aeromonas hydrophila diarrheal isolate SSU have been molecularly characterized in our laboratory. One of these enterotoxins is cytotoxic in nature, whereas the other two are cytotonic enterotoxins, one of them heat labile and the other heat stable. Earlier, by developing an isogenic mutant, we demonstrated the role of a cytotoxic enterotoxin in causing systemic infection in mice. In the present study, we evaluated the role of these three enterotoxins in evoking diarrhea in a murine model by developing various combinations of enterotoxin gene-deficient mutants by marker-exchange mutagenesis. A total of six isogenic mutants were prepared in a cytotoxic enterotoxin gene (act)-positive or -negative background strain of A. hydrophila. We developed two single knockouts with truncation in either the heat-labile (alt) or the heat-stable (ast) cytotonic enterotoxin gene; three double knockouts with truncations of genes encoding (i) alt and ast, (ii) act and alt, and (iii) act and ast genes; and a triple-knockout mutant with truncation in all three genes, act, alt, and ast. The identity of these isogenic mutants developed by double-crossover homologous recombination was confirmed by Southern blot analysis. Northern and Western blot analyses revealed that the expression of different enterotoxin genes in the mutants was correspondingly abrogated. We tested the biological activity of these mutants in a diet-restricted and antibiotic-treated mouse model with a ligated ileal loop assay. Our data indicated that all of these mutants had significantly reduced capacity to evoke fluid secretion compared to that of wild-type A. hydrophila; the triple-knockout mutant failed to induce any detectable level of fluid secretion. The biological activity of selected A. hydrophila mutants was restored after complementation. Taken together, we have established a role for three enterotoxins in A. hydrophila-induced gastroenteritis in a mouse model with the greatest contribution from the cytotoxic enterotoxin Act, followed by the Alt and Ast cytotonic enterotoxins.
我们实验室已对嗜水气单胞菌腹泻分离株SSU的三种肠毒素进行了分子特征分析。其中一种肠毒素本质上具有细胞毒性,而另外两种是细胞紧张性肠毒素,一种对热不稳定,另一种对热稳定。此前,通过构建同基因突变体,我们证明了一种细胞毒性肠毒素在小鼠全身感染中的作用。在本研究中,我们通过标记交换诱变构建了多种肠毒素基因缺陷突变体组合,以评估这三种肠毒素在小鼠模型中引发腹泻的作用。在嗜水气单胞菌细胞毒性肠毒素基因(act)阳性或阴性背景菌株中总共制备了六个同基因突变体。我们构建了两个单基因敲除突变体,分别是热不稳定(alt)或热稳定(ast)细胞紧张性肠毒素基因发生截断;三个双基因敲除突变体,其编码基因的截断情况分别为:(i)alt和ast,(ii)act和alt,以及(iii)act和ast基因;还有一个三基因敲除突变体,act、alt和ast这三个基因均发生截断。通过Southern印迹分析证实了通过双交换同源重组构建的这些同基因突变体的身份。Northern和Western印迹分析表明,突变体中不同肠毒素基因的表达相应地被消除。我们在饮食受限且经抗生素处理的小鼠模型中采用结扎回肠袢试验测试了这些突变体的生物学活性。我们的数据表明,与野生型嗜水气单胞菌相比,所有这些突变体诱发液体分泌的能力均显著降低;三基因敲除突变体未能诱导出任何可检测到的液体分泌水平。所选嗜水气单胞菌突变体在互补后恢复了生物学活性。综上所述,我们在小鼠模型中确定了三种肠毒素在嗜水气单胞菌诱导的胃肠炎中的作用,其中细胞毒性肠毒素Act的贡献最大,其次是Alt和Ast细胞紧张性肠毒素。