Rakin A, Saken E, Harmsen D, Heesemann J
Institut für Hygiene und Mikrobiologie, Universität Würzburg, Germany.
Mol Microbiol. 1994 Jul;13(2):253-63. doi: 10.1111/j.1365-2958.1994.tb00420.x.
The iron-repressible outer membrane protein FyuA of Yersinia enterocolitica operates as a receptor with dual function: (i) as a receptor for the Y. pestis bacteriocin pesticin, and (ii) as a receptor for yersiniabactin, a siderophore that is produced by mouse-virulent Y. enterocolitica strains of biogroup IB. Cloning of the FyuA-encoding gene was achieved by mobilization of a genomic cosmid library of the pesticin-sensitive and mouse-virulent Y. enterocolitica O:8 strain WA into the pesticin-resistant WA fyuA mutant and subsequent in vivo selection of transconjugants for the ability to survive and multiply in mice (phenotype mouse virulence). The reisolated transconjugants which survived in mice for 3 d harboured a unique cosmid and phenotypically were pesticin sensitive. From this cosmid a 2650 bp SalI-PstI fragment conferring pesticin sensitivity was subcloned. Sequencing of this DNA fragment revealed a single open reading frame of 2022 bp, which encodes a deduced polypeptide of 673 amino acids with a predicted molecular mass of 73,677 Da. Cleavage of a putative signal sequence composed of 22 amino acids should lead to a mature protein of 651 amino acids with a molecular mass of 71,368 Da. The open reading frame is preceded by a sequence which shares homology with the postulated consensus Fur iron-repressor protein-binding site. FyuA shows homology to other iron-regulated TonB-dependent outer membrane proteins with receptor functions (e.g. BtuB, CirA, FepA, IutA, FhuA, FoxA, FcuA). On the basis of multiple alignment of amino acid sequences of FyuA and other TonB-dependent receptors, a phylogenetic tree was constructed, demonstrating that FyuA probably belongs to the citrate subfamily or represents a new subfamily of TonB-dependent receptors. Moreover, by complementation of the WA fyuA mutant by the cloned fyuA gene, yersiniabactin uptake and mouse virulence were restored. These studies demonstrate that the cloned pesticin/yersiniabactin receptor FyuA of Y. enterocolitica has the typical features of iron-regulated TonB-dependent outer membrane receptors for siderophores and bacteriocins and is required for mouse virulence.
小肠结肠炎耶尔森菌的铁抑制性外膜蛋白FyuA具有双重功能:(i)作为鼠疫耶尔森菌细菌素鼠疫菌素的受体;(ii)作为yersiniabactin的受体,yersiniabactin是由生物群IB的小鼠毒力小肠结肠炎耶尔森菌菌株产生的一种铁载体。通过将对鼠疫菌素敏感且对小鼠有毒力的小肠结肠炎耶尔森菌O:8菌株WA的基因组黏粒文库转移至抗鼠疫菌素的WA fyuA突变体中,并随后在体内选择能够在小鼠中存活和繁殖的接合子(表型为小鼠毒力),实现了编码FyuA基因的克隆。重新分离出的在小鼠中存活3天的接合子携带一个独特的黏粒,且表型上对鼠疫菌素敏感。从该黏粒中,亚克隆出一个赋予鼠疫菌素敏感性的2650 bp SalI - PstI片段。对该DNA片段进行测序,揭示了一个2022 bp的单一开放阅读框,其编码一个推导的由673个氨基酸组成的多肽,预测分子量为73,677 Da。由22个氨基酸组成的假定信号序列的切割应导致产生一个由651个氨基酸组成、分子量为71,368 Da的成熟蛋白。该开放阅读框之前有一段与假定的Fur铁抑制蛋白结合位点共有序列具有同源性的序列。FyuA与其他具有受体功能的铁调节TonB依赖性外膜蛋白(如BtuB、CirA、FepA、IutA、FhuA、FoxA、FcuA)具有同源性。基于FyuA和其他TonB依赖性受体的氨基酸序列多重比对,构建了系统发育树,表明FyuA可能属于柠檬酸盐亚家族或代表TonB依赖性受体的一个新亚家族。此外,通过克隆的fyuA基因对WA fyuA突变体进行互补,恢复了yersiniabactin摄取和小鼠毒力。这些研究表明,克隆的小肠结肠炎耶尔森菌鼠疫菌素/yersiniabactin受体FyuA具有铁调节TonB依赖性外膜受体对铁载体和细菌素的典型特征,并且是小鼠毒力所必需的。