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小鼠肠袢对肉毒杆菌C2毒素的反应:非连接蛋白成分协同诱导的肠毒素活性

Response of mouse intestinal loop to botulinum C2 toxin: enterotoxic activity induced by cooperation of nonlinked protein components.

作者信息

Ohishi I

出版信息

Infect Immun. 1983 May;40(2):691-5. doi: 10.1128/iai.40.2.691-695.1983.

Abstract

Botulinum C2 toxin, which is composed of two nonlinked protein components, components I and II, induced fluid accumulation in mouse intestinal loops. The secretory response to C2 toxin was initiated after a lag period of 1 to 2 h and increased gradually for at least 10 h. The activity of C2 toxin was enhanced by treatment with trypsin and abolished by neutralization with anti-component I or anti-component II sera. Neither component I nor component II alone induced the fluid accumulation in intestinal loops. The intestinal loop activity was demonstrated with the culture supernatants of strains of Clostridium botulinum types C and D that produced C2 toxin, but not with culture supernatants of strains that did not. None of the botulinum type A through F neurotoxins induced fluid accumulation in mouse intestinal loops. The results indicate that, in addition to lethal and vascular permeability activities, C2 toxin has an enterotoxic activity for which the cooperation of components I and II is necessary. The fluid accumulation in intestinal loops inoculated with C2 toxin was not diminished by removal of the toxin from the loops. Moreover, the secretory response was positive when intestinal lumina were exposed to component II followed by the removal of the component and inoculation with component I, but it was negative when the intestinal lumina were exposed to component I followed by the removal of the component and inoculation with component II. These results suggest that the secretory response of mouse intestinal loops to C2 toxin is induced by the binding of component II to the epithelial cell surfaces of the intestines and the consequent binding or penetration of component I into the cells.

摘要

肉毒杆菌C2毒素由两种非连接的蛋白质成分,即成分I和成分II组成,可在小鼠肠袢中诱导液体蓄积。对C2毒素的分泌反应在1至2小时的延迟期后开始,并至少持续10小时逐渐增加。用胰蛋白酶处理可增强C2毒素的活性,而用抗成分I或抗成分II血清中和则可消除其活性。单独的成分I或成分II均未诱导肠袢中的液体蓄积。用产生C2毒素的C型和D型肉毒杆菌菌株的培养上清液可证明肠袢活性,而未产生C2毒素的菌株的培养上清液则不能证明。A至F型肉毒杆菌神经毒素均未在小鼠肠袢中诱导液体蓄积。结果表明,除了致死和血管通透性活性外,C2毒素还具有肠毒素活性,其成分I和成分II的协同作用是必需的。接种C2毒素的肠袢中的液体蓄积不会因从肠袢中去除毒素而减少。此外,当肠腔暴露于成分II后再去除该成分并接种成分I时,分泌反应为阳性,但当肠腔暴露于成分I后再去除该成分并接种成分II时,分泌反应为阴性。这些结果表明,小鼠肠袢对C2毒素的分泌反应是由成分II与肠上皮细胞表面结合以及随后成分I与细胞的结合或渗透所诱导的。

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