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产气荚膜梭菌洛塔毒素的致死和皮肤坏死活性:由两个非连锁成分协同诱导的生物学活性。

Lethal and dermonecrotic activities of Clostridium perfringens lota toxin: biological activities induced by cooperation of two nonlinked components.

作者信息

Sakurai J, Kobayashi K

机构信息

Department of Microbiology, Faculty of Pharmaceutical Sciences, Tokushima Bunri University, Japan.

出版信息

Microbiol Immunol. 1995;39(4):249-53. doi: 10.1111/j.1348-0421.1995.tb02197.x.

Abstract

The effect of separate injections of two components of Clostridium perfringens iota toxin, designated Ia and Ib components, on the biological activities of the toxin was investigated. The intravenous injection of one component within 120 min after the injection of the other component killed mice. The activity of iota toxin was abolished by anti-Ia or anti-Ib antiserum. On the other hand, when Ib component was intravenously administered to mice given anti-Ia antiserum within 120 min after the intravenous injection of Ia component, the lethal activity was completely neutralized, but when Ia component was injected into mice that were given anti-Ib antiserum over 5 min after the injection of Ib component, the activity was not neutralized. The separate injections of Ia and Ib components in skin of guinea pigs indicated dermonecrosis at the injection site of Ib components, but not at the site of Ia components. Furthermore, when one component was intradermally injected in guinea pigs and then the other intraperitoneally, the dermonecrotic activity of the toxin was observed at the intradermal injection site of Ib component, but not at that of Ia component. From the data, it appears that the lethal and dermonecrotic activities of iota toxin are initiated by the binding of Ib component to specific sites on tissues.

摘要

研究了产气荚膜梭菌iota毒素的两种成分(分别称为Ia和Ib成分)单独注射对毒素生物活性的影响。在注射另一种成分后120分钟内静脉注射其中一种成分可致小鼠死亡。抗Ia或抗Ib抗血清可消除iota毒素的活性。另一方面,在静脉注射Ia成分后120分钟内给小鼠静脉注射抗Ia抗血清,再静脉注射Ib成分,致死活性可被完全中和,但在注射Ib成分5分钟后给小鼠注射抗Ib抗血清,再注射Ia成分,其活性未被中和。在豚鼠皮肤中分别注射Ia和Ib成分,结果显示Ib成分注射部位出现皮肤坏死,而Ia成分注射部位未出现。此外,当在豚鼠皮内注射一种成分,然后腹腔注射另一种成分时,在Ib成分皮内注射部位观察到毒素的皮肤坏死活性,而在Ia成分注射部位未观察到。根据这些数据,看来iota毒素的致死和皮肤坏死活性是由Ib成分与组织上的特定部位结合引发的。

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