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在小鼠模型中,产气荚膜梭菌ε毒素的致死作用被α毒素和穿孔毒素增强。

Lethal effects of Clostridium perfringens epsilon toxin are potentiated by alpha and perfringolysin-O toxins in a mouse model.

作者信息

Fernandez-Miyakawa Mariano E, Jost B Helen, Billington Stephen J, Uzal Francisco A

机构信息

California Animal Health and Food Safety Laboratory System, San Bernardino Branch, School of Veterinary Medicine, University of California, Davis, 105 W Central Avenue, San Bernardino, CA 92408, USA.

出版信息

Vet Microbiol. 2008 Mar 18;127(3-4):379-85. doi: 10.1016/j.vetmic.2007.09.013. Epub 2007 Oct 2.

Abstract

Epsilon toxin (ETX) is the most important virulence factor of Clostridium perfringens type D. Two other important toxins, alpha toxin (CPA) and perfringolysin-O (PFO), are encoded and potentially produced by most C. perfringens type D isolates. The biological effects of these toxins are dissimilar although they are all lethal. Since the possible interaction of these toxins during infection is unknown, the effects of CPA and PFO on the lethal activity of ETX were studied in a mouse model. Mice were injected intravenously or intragastrically with CPA or PFO with or without ETX. Sublethal doses of CPA or PFO did not affect the lethality of ETX when either was injected together with the latter intravenously. However, sublethal or lethal doses of CPA or PFO resulted in reduction of the survival time of mice injected simultaneously with ETX when compared with the intravenous effect of ETX injected alone. When PFO was inoculated intragastrically with ETX, a reduction of the survival time was observed. CPA did not alter the survival time when inoculated intragastrically with ETX. The results of the present study suggest that both CPA and PFO have the potential to enhance the ETX lethal effects during enterotoxemia in natural hosts such as sheep and goats.

摘要

ε毒素(ETX)是产气荚膜梭菌D型最重要的毒力因子。另外两种重要毒素,α毒素(CPA)和穿孔素-O(PFO),大多数产气荚膜梭菌D型分离株都能编码并可能产生。尽管这些毒素都具有致死性,但其生物学效应并不相同。由于这些毒素在感染过程中可能的相互作用尚不清楚,因此在小鼠模型中研究了CPA和PFO对ETX致死活性的影响。给小鼠静脉内或胃内注射CPA或PFO,同时或不注射ETX。当与ETX一起静脉内注射时,亚致死剂量的CPA或PFO不会影响ETX的致死性。然而,与单独静脉注射ETX的效果相比,亚致死或致死剂量的CPA或PFO会导致与ETX同时注射的小鼠存活时间缩短。当PFO与ETX一起胃内接种时,观察到存活时间缩短。当CPA与ETX一起胃内接种时,不会改变存活时间。本研究结果表明,CPA和PFO都有可能在绵羊和山羊等天然宿主的肠毒血症期间增强ETX的致死作用。

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