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纤连蛋白结合蛋白在马链球菌兽疫亚种发病机制中的作用。

Contribution of fibronectin-binding protein to pathogenesis of Streptococcus equi ssp. zooepidemicus.

机构信息

Key Lab of Animal Bacteriology, Ministry of Agriculture, Nanjing Agricultural University, Nanjing, China.

出版信息

Pathog Dis. 2013 Apr;67(3):174-83. doi: 10.1111/2049-632X.12029. Epub 2013 Mar 18.

DOI:10.1111/2049-632X.12029
PMID:23620180
Abstract

Streptococcus equi ssp. zooepidemicus (S. zooepidemicus) is responsible for a wide variety of infections in many species. Fibronectin-binding protein is a bacterial cell surface protein, which specifically binds fibronectin (FN). Considering the specific role of FN-binding protein in host-pathogen interactions, we investigated the function of a novel FN-binding domain in the FN-binding protein (FNZ) of S. zooepidemicus. Five recombinant FNZ gene fragments [N1 (amino acids, 38-197), N2 (amino acids, 38-603), N3 (amino acids, 41-315), N4 (amino acids, 192-370), and N5 (amino acids, 38-225)] were expressed in Escherichia coli, and their FN-binding activities were tested. The results showed that amino acids 192-225 in the NH2 -terminal region of FNZ could be responsible for binding fibronectin. The FNZ knockout mutant was constructed in S. zooepidemicus, which results in the reduced capacity to adhere to HEp-2 cell, defective virulence in vivo, decreased biofilm formation, and decreased colonization capacity in blood, liver, lung, and spleen tissues of mice as compared to the wild type. These results suggest that FNZ participates in biofilm formation, FN binding, cell adhesion, and pathogenesis of S. zooepidemicus. Furthermore, this work offers a novel FN-binding domain within FNZ, which will help in further characterization of S. zooepidemicus FN-binding properties.

摘要

马链球菌兽疫亚种(S. zooepidemicus)可引起多种物种的广泛感染。纤连蛋白结合蛋白是一种细菌表面蛋白,可特异性结合纤连蛋白(FN)。鉴于 FN 结合蛋白在宿主-病原体相互作用中的特定作用,我们研究了马链球菌兽疫亚种 FN 结合蛋白(FNZ)中新型 FN 结合结构域的功能。我们在大肠杆菌中表达了 5 个重组 FNZ 基因片段[N1(氨基酸,38-197)、N2(氨基酸,38-603)、N3(氨基酸,41-315)、N4(氨基酸,192-370)和 N5(氨基酸,38-225)],并测试了它们与纤连蛋白的结合活性。结果表明,FNZ NH2-末端区域的氨基酸 192-225 可能负责结合纤连蛋白。我们构建了马链球菌兽疫亚种 FNZ 敲除突变体,与野生型相比,该突变体黏附 HEp-2 细胞的能力降低,体内毒力下降,生物膜形成减少,在血液、肝脏、肺部和脾脏组织中的定植能力降低。这些结果表明 FNZ 参与了生物膜形成、FN 结合、细胞黏附和马链球菌兽疫亚种的发病机制。此外,本研究发现了 FNZ 内的新型 FN 结合结构域,这将有助于进一步研究马链球菌兽疫亚种的 FN 结合特性。

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