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The role of toxin A and toxin B in Clostridium difficile-associated disease

机译:毒素A和毒素B在艰难梭菌相关疾病中的作用

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摘要

Recently, we constructed and characterized isogenic tcdA and tcdB mutants of a virulent Clostridium difficile strain and used a hamster model of disease to demonstrate that toxin B, not toxin A, is essential for virulence of this emerging pathogen. Earlier studies had shown that purified toxin A alone was able to induce C. difficile disease pathology and that purified toxin B was not effective unless it was co-administered with toxin A, suggesting that the toxins act synergistically. In this addendum we discuss this paradigm-shifting conclusion in the context of current strain epidemiology, particularly with respect to naturally occurring toxin A-negative, toxin B-positive isolates and the NAP1/027 epidemic isolates. The role of toxin receptors and how variant toxins might exert their effects is also discussed in relation to the published data. We conclude that it is critical to use the natural infection process to dissect the role of toxins in disease, and that future studies are contingent on such work. The impact and importance of animal models of C. difficile virulence are therefore considered within this frame of reference.
机译:最近,我们构建并鉴定了艰难梭状芽胞杆菌毒性菌株的等基因tcdA和tcdB突变体,并使用疾病的仓鼠模型证明毒素B(而非毒素A)对于这种新兴病原体的毒力至关重要。较早的研究表明,纯化的毒素A单独能够诱导艰难梭菌疾病病理,并且纯化的毒素B除非与毒素A共同施用,否则是无效的,这表明该毒素具有协同作用。在此附录中,我们在当前菌株流行病学的背景下,特别是在自然产生的毒素A阴性,毒素B阳性分离株和NAP1 / 027流行分离株方面,讨论了这种模式转变的结论。还针对已发表的数据讨论了毒素受体的作用以及变异毒素如何发挥作用。我们得出结论,至关重要的是利用自然感染过程来剖析毒素在疾病中的作用,并且未来的研究取决于这种工作。因此,在该参考框架内考虑了艰难梭菌毒力动物模型的影响和重要性。

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