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炭疽

Anthrax.

作者信息

Mock M, Fouet A

机构信息

Toxines et Pathogénie Bactérienne, (CNRS URA 2172), Institut Pasteur, Paris Cedex 15, France.

出版信息

Annu Rev Microbiol. 2001;55:647-71. doi: 10.1146/annurev.micro.55.1.647.

Abstract

Bacillus anthracis was shown to be the etiological agent of anthrax by R. Koch and L. Pasteur at the end of the nineteenth century. The concepts on which medical microbiology are based arose from their work on this bacterium. The link between plasmids and major virulence factors of B. anthracis was not discovered until the 1980s. The three toxin components are organized in two A-B type toxins, and the bacilli are covered by an antiphagocytic polyglutamic capsule. Structure-function analysis of the toxins indicated that the common B-domain binds to a ubiquitous cell receptor and forms a heptamer after proteolytic activation. One enzyme moiety is an adenylate cyclase and the other is a Zn(2+) metalloprotease, which is able to cleave MAPKKs. The capsule covers an S-layer sequentially composed of two distinct proteins. Knowledge of the toxins facilitates the design of safer veterinary vaccines. Spore-structure analysis could contribute to the improvement of human nonliving vaccines. The phylogeny of B. anthracis within the Bacillus cereus group is also reviewed.

摘要

19世纪末,R. 科赫和L. 巴斯德证明炭疽芽孢杆菌是炭疽病的病原体。医学微生物学所基于的概念就源于他们对这种细菌的研究。直到20世纪80年代,人们才发现炭疽芽孢杆菌的质粒与主要毒力因子之间的联系。三种毒素成分被组织成两种A-B型毒素,杆菌被一种抗吞噬的聚谷氨酸荚膜所覆盖。毒素的结构-功能分析表明,共同的B结构域与一种普遍存在的细胞受体结合,并在蛋白水解激活后形成七聚体。一种酶部分是腺苷酸环化酶,另一种是能够切割丝裂原活化蛋白激酶激酶(MAPKKs)的锌(2+)金属蛋白酶。荚膜覆盖着一个依次由两种不同蛋白质组成的S层。对毒素的了解有助于设计更安全的兽用疫苗。芽孢结构分析可能有助于改进人类非活性疫苗。本文还综述了炭疽芽孢杆菌在蜡样芽孢杆菌群中的系统发育。

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