产气荚膜梭菌
毒力
生物
微生物学
毒素
毒力因子
突变体
艰难梭菌毒素B
野生型
病毒学
基因
艰难梭菌毒素A
遗传学
艰难梭菌
细菌
抗生素
作者
Anthony L. Keyburn,John D. Boyce,Paola K. Vaz,Trudi L. Bannam,Mark Ford,Dane Parker,Antonio Di Rubbo,Julian I. Rood,Robert J. Moore
出处
期刊:PLOS Pathogens
[Public Library of Science]
日期:2008-02-05
卷期号:4 (2): e26-e26
被引量:619
标识
DOI:10.1371/journal.ppat.0040026
摘要
For over 30 years a phospholipase C enzyme called alpha-toxin was thought to be the key virulence factor in necrotic enteritis caused by Clostridium perfringens. However, using a gene knockout mutant we have recently shown that alpha-toxin is not essential for pathogenesis. We have now discovered a key virulence determinant. A novel toxin (NetB) was identified in a C. perfringens strain isolated from a chicken suffering from necrotic enteritis (NE). The toxin displayed limited amino acid sequence similarity to several pore forming toxins including beta-toxin from C. perfringens (38% identity) and alpha-toxin from Staphylococcus aureus (31% identity). NetB was only identified in C. perfringens type A strains isolated from chickens suffering NE. Both purified native NetB and recombinant NetB displayed cytotoxic activity against the chicken leghorn male hepatoma cell line LMH; inducing cell rounding and lysis. To determine the role of NetB in NE a netB mutant of a virulent C. perfringens chicken isolate was constructed by homologous recombination, and its virulence assessed in a chicken disease model. The netB mutant was unable to cause disease whereas the wild-type parent strain and the netB mutant complemented with a wild-type netB gene caused significant levels of NE. These data show unequivocally that in this isolate a functional NetB toxin is critical for the ability of C. perfringens to cause NE in chickens. This novel toxin is the first definitive virulence factor to be identified in avian C. perfringens strains capable of causing NE. Furthermore, the netB mutant is the first rationally attenuated strain obtained in an NE-causing isolate of C. perfringens; as such it has considerable vaccine potential.
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