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Typing of Clostridium Perfringens by in Vitro Amplification of Toxin Genes

机译:通过体外毒素基因扩增对产气荚膜梭菌的分型

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摘要

The strains of Clostridium perfringens are classified according to major toxins produced. Classically, this determination involves the seroneutralization of their lethal effect in mice. However, this method requires specific antisera and a large number of mice. In this work, a new typing method was developed based on the amplification of toxin genes by polymerase chain reaction (PCR). By combination of several pairs of primers, the toxinotype of a Cl. perfringens strain was determined by looking at the pattern of bands on an agarose gel electrophoresis. This mixture contained primers amplifying simultaneously a part of alpha-toxin, beta-toxin, epsilon-toxin and enterotoxin genes. In order to distinguish between toxinotype A and E, the l-toxin gene fragment must be amplified in a separate PCR reaction. Moreover, with the primers combination, in most cases, a PCR product corresponding to the alpha-toxin gene was obtained from direct enrichments of animal intestinal contents.
机译:产气荚膜梭菌菌株根据产生的主要毒素分类。经典地,这种确定涉及它们在小鼠中的致死作用的血清素化。但是,该方法需要特异性抗血清和大量小鼠。在这项工作中,基于通过聚合酶链反应(PCR)扩增毒素基因的方法,开发了一种新的分型方法。通过几对引物的组合,Cl的毒素型。通过在琼脂糖凝胶电泳上观察条带的模式来确定产气荚膜炎菌株。该混合物含有同时扩增部分α-毒素,β-毒素,ε-毒素和肠毒素基因的引物。为了区分A型和E型,必须在单独的PCR反应中扩增l-毒素基因片段。而且,通过引物组合,在大多数情况下,从动物肠内容物的直接富集获得对应于α-毒素基因的PCR产物。

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