Clostridium Perfringens Toxins Involved in Mammalian Veterinary Diseases

F. Uzal, J. Vidal, B. McClane, A. Gurjar
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引用次数: 127

Abstract

Clostridium perfringens is a gram-positive anaerobic rod that is classified into 5 toxinotypes (A, B, C, D, and E) according to the production of 4 major toxins, namely alpha (CPA), beta (CPB), epsilon (ETX) and iota (ITX). However, this microorganism can produce up to 16 toxins in various combinations, including lethal toxins such as perfringolysin O (PFO), enterotoxin (CPE), and beta2 toxin (CPB2). Most diseases caused by this microorganism are mediated by one or more of these toxins. The role of CPA in intestinal disease of mammals is controversial and poorly documented, but there is no doubt that this toxin is essential in the production of gas gangrene of humans and several animal species. CPB produced by C. perfringens types B and C is responsible for necrotizing enteritis and enterotoxemia mainly in neonatal individuals of several animal species. ETX produced by C. perfringens type D is responsible for clinical signs and lesions of enterotoxemia, a predominantly neurological disease of sheep and goats. The role of ITX in disease of animals is poorly understood, although it is usually assumed that the pathogenesis of intestinal diseases produced by C. perfringens type E is mediated by this toxin. CPB2, a necrotizing and lethal toxin that can be produced by all types of C. perfringens, has been blamed for disease in many animal species, but little information is currently available to sustain or rule out this claim. CPE is an important virulence factor for C. perfringens type A gastrointestinal disease in humans and dogs; however, the data implicating CPE in other animal diseases remains ambiguous. PFO does not seem to play a direct role as the main virulence factor for animal diseases, but it may have a synergistic role with CPA-mediated gangrene and ETX-mediated enterotoxemia. The recent improvement of animal models for C. perfringens infection and the use of toxin gene knock-out mutants have demonstrated the specific pathogenic role of several toxins of C. perfringens in animal disease. These research tools are helping us to establish the role of each C. perfringens toxin in animal disease, to investigate the in vivo mechanism of action of these toxins, and to develop more effective vaccines against diseases produced by these microorganisms.
与哺乳动物兽医疾病有关的产气荚膜梭菌毒素
产气荚膜梭菌是革兰氏阳性厌氧棒,根据产生α (CPA)、β (CPB)、epsilon (ETX)、iota (ITX) 4种主要毒素,将其分为a、B、C、D、E 5种毒素型。然而,这种微生物可以产生多达16种不同组合的毒素,包括致命毒素,如perfringolysin O (PFO),肠毒素(CPE)和β 2毒素(CPB2)。这种微生物引起的大多数疾病都是由一种或多种毒素介导的。CPA在哺乳动物肠道疾病中的作用是有争议的,文献也很少,但毫无疑问,这种毒素在人类和一些动物物种的气性坏疽的产生中是必不可少的。产气荚膜荚膜杆菌B型和C型产生的CPB主要在几种动物的新生儿个体中引起坏死性肠炎和肠毒血症。产气荚膜梭菌D型产生的ETX可导致肠毒血症的临床症状和病变,肠毒血症是绵羊和山羊的一种主要神经系统疾病。ITX在动物疾病中的作用尚不清楚,尽管通常认为E型产气荚膜原梭菌产生的肠道疾病的发病机制是由这种毒素介导的。CPB2是一种坏死性和致命的毒素,所有类型的产气荚膜梭菌都能产生这种毒素,它被认为是许多动物疾病的罪魁祸首,但目前几乎没有信息支持或排除这种说法。CPE是人犬A型产气荚膜荚膜梭菌胃肠道疾病的重要毒力因子;然而,CPE与其他动物疾病相关的数据仍然不明确。PFO似乎并不直接作为动物疾病的主要毒力因子,但它可能与cpa介导的坏疽和etx介导的肠毒血症有协同作用。最近改进的产气荚膜梭菌感染动物模型和毒素基因敲除突变体的使用已经证明了产气荚膜梭菌的几种毒素在动物疾病中的特定致病作用。这些研究工具正在帮助我们确定每种产气荚膜荚膜原细菌毒素在动物疾病中的作用,研究这些毒素的体内作用机制,并开发针对这些微生物产生的疾病的更有效的疫苗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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