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绵羊腐蹄病的发病机制。

The pathogenesis of ovine footrot.

机构信息

ARC Centre of Excellence in Structural and Functional Microbial Genomics, Department of Microbiology, Monash University, Clayton, Victoria 3800, Australia.

出版信息

Vet Microbiol. 2011 Nov 21;153(1-2):59-66. doi: 10.1016/j.vetmic.2011.04.005. Epub 2011 Apr 14.

Abstract

Ovine footrot is a contagious and debilitating disease that is of major economic significance to the sheep meat and wool industries. The causative bacterium is the gram negative anaerobe Dichelobacter nodosus. Research that has used a classical molecular genetics approach has led to major advances in our understanding of the role of the key virulence factors of D. nodosus in the disease process. D. nodosus strains produce polar type IV fimbriae and extracellular serine proteases. Mutagenesis of the fimbrial subunit gene fimA and the pilT gene, which is required for fimbrial retraction, and subsequent testing of these mutants in sheep virulence trials has shown that type IV fimbriae-mediated twitching motility is essential for virulence. The extracellular protease genes aprV2, aprV5 and bprV have also been mutated. Analysis of these mutants has shown that ArpV5 is the major extracellular protease and that AprV2 is the thermostable protease that is responsible for the extracellular elastase activity. Structural analysis of AprV2 has revealed that it contains several novel loops, one of which appears to act as an exosite that may modulate substrate accessibility. Finally, virulence experiments in sheep have shown that the AprV2 protease is required for virulence.

摘要

绵羊腐蹄病是一种传染性和衰弱性疾病,对羊肉和羊毛产业具有重大的经济意义。致病细菌是革兰氏阴性厌氧菌坏死梭杆菌。使用经典分子遗传学方法的研究使我们对坏死梭杆菌关键毒力因子在疾病过程中的作用有了重大的认识。坏死梭杆菌菌株产生极性 IV 型菌毛和细胞外丝氨酸蛋白酶。对菌毛亚基基因 fimA 和 pilT 进行诱变,pilT 基因是菌毛缩回所必需的,随后在绵羊毒力试验中对这些突变体进行测试,表明 IV 型菌毛介导的扭动运动对于毒力是必需的。细胞外蛋白酶基因 aprV2、aprV5 和 bprV 也已发生突变。对这些突变体的分析表明,ArpV5 是主要的细胞外蛋白酶,而 AprV2 是负责细胞外弹性蛋白酶活性的耐热蛋白酶。AprV2 的结构分析表明,它含有几个新的环,其中一个似乎作为一个变构部位,可能调节底物的可及性。最后,绵羊的毒力实验表明,AprV2 蛋白酶是毒力所必需的。

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