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首页> 外文期刊>Journal of bacteriology >The AsaP1 Peptidase of Aeromonas salmonicida subsp. achromogenes Is a Highly Conserved Deuterolysin Metalloprotease (Family M35) and a Major Virulence Factor
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The AsaP1 Peptidase of Aeromonas salmonicida subsp. achromogenes Is a Highly Conserved Deuterolysin Metalloprotease (Family M35) and a Major Virulence Factor

机译:鲑鱼气单胞菌亚种的AsaP1肽酶。色原是高度保守的氘代溶血素金属蛋白酶(家族M35)和主要毒力因子

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Infections by the bacterium Aeromonas salmonicida subsp. achromogenes cause significant disease in a number of fish species. In this study, we showed that AsaP1, a toxic 19-kDa metallopeptidase produced by A. salmonicida subsp. achromogenes, belongs to the group of extracellular peptidases (Aeromonas type) (MEROPS ID M35.003) of the deuterolysin family of zinc-dependent aspzincin endopeptidases. The structural gene of AsaP1 was sequenced and found to be highly conserved among gram-negative bacteria. An isogenic ΔasaP1 A. salmonicida subsp. achromogenes strain was constructed, and its ability to infect fish was compared with that of the wild-type (wt) strain. The ΔasaP1 strain was found to infect Arctic charr, Atlantic salmon, and Atlantic cod, but its virulence was decreased relative to that of the wt strain. The 50% lethal dose of the AsaP1 mutant was 10-fold higher in charr and 5-fold higher in salmon than that of the wt strain. The pathology induced by the AsaP1-deficient strain was also different from that of the wt strain. Furthermore, the mutant established significant bacterial colonization in all observed organs without any signs of a host response in the infected tissue. AsaP1 is therefore the first member of the M35 family that has been shown to be a bacterial virulence factor.
机译:细菌沙门气单胞菌亚种的感染。生色团在许多鱼类中引起重大疾病。在这项研究中,我们表明AsaP1是 A产生的一种有毒的19 kDa金属肽酶。鲑科亚种 achromogenes ,属于锌依赖性天冬氨酸锌内肽酶的氘申溶素家族的细胞外肽酶( Aeromonas 型)(MEROPS ID M35.003)。对AsaP1的结构基因进行了测序,发现在革兰氏阴性细菌中高度保守。等位基因Δ asaP1 A.salicicida 构建了无色系菌株,并将其感染鱼类的能力与野生型(wt)菌株进行了比较。发现Δ asaP1 菌株可感染北极鲑,大西洋鲑和大西洋鳕鱼,但其毒力相对于wt菌株有所降低。与wt菌株相比,AsaP1突变体的50%致死剂量在charr中高10倍,在鲑鱼中高5倍。由AsaP1缺陷型菌株引起的病理也与wt菌株不同。此外,该突变体在所有观察到的器官中均建立了明显的细菌定植,而在感染组织中没有任何宿主应答的迹象。因此,AsaP1是M35家族的第一个成员,已被证明是细菌毒力因子。

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