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鼠伤寒沙门氏菌血清型 Typhi 的 TonB 依赖性转运蛋白 YncD 具有疫苗潜力。

A TonB dependent transporter YncD of Salmonella enterica Serovar Typhi possesses vaccine potential.

机构信息

Department of Clinical Laboratory, The First Dongguan Affiliated Hospital of Guangdong Medical University, Dongguan, Guangdong province, 523710, China.

Dongguan Key Laboratory of Pathogenesis and Experimental Diagnosis of Infectious Diseases, The First Dongguan Affiliated Hospital of Guangdong Medical University, Dongguan, Guangdong province, 523710, China.

出版信息

World J Microbiol Biotechnol. 2024 Mar 12;40(4):131. doi: 10.1007/s11274-024-03937-9.

Abstract

Multiple TonB dependent transporters (TBDTs) contribute to bacterial virulence due to the importance roles that their substrates play in bacterial growth, and possess vaccine potential. A putative TBDT, YncD, had been identified as one of in vivo induced antigens during human infection of typhoid fever, and is required for the pathogenicity of Salmonella enterica Serovar Typhi. The present study was aimed to determine the function and immunogenicity of YncD. Homologous recombination method was used to construct an yncD-deletion mutant and cirA-iroN-fepA-deletion mutant from the wild-type S. Typhi Ty2. The growth of mutants and the wild-type strain were assessed in iron-deficient medium, as well as in human macrophage cells. Recombinant YncD protein was expressed and purified using Ni-NTA affinity chromatography and anion exchange. A mouse model was then used to evaluate the immunogenicity and protection efficacy of the recombinant YncD. Antibody levels, serum bactericidal efficiency, passive immune protection, opsonophagocysis were assayed to analyse the immunoprotection mechanism of the recombinant YncD. Our results showed that YncD is associated with the iron-uptake of S. Typhi. The yncD-deletion mutant displayed impaired growth in iron-deficient medium, comparable to that the cirA-iroN-fepA-deletion mutant did. The mutation of yncD markedly decreased bacterial growth within human macrophage cells. Moreover, subcutaneous immunization of mice with recombinant YncD elicited high levels of specific anti-YncD IgG, IgG1 and IgG2a, which protected the immunized mice against the intraperitoneal challenge of S. Typhi, and decreased bacterial burdens in the livers and spleens of the infected mice. Passive immunization using the immunized sera also efficiently protected the mice from the challenge of S. Typhi. Moreover, the immunized sera enhanced in vitro bactericidal activity of complement, and opsonophagocytosis. Our results showed that YncD displays a role in the iron-uptake of S. Typhi and possesses immunogenicity.

摘要

多种 TonB 依赖转运蛋白(TBDT)因其底物在细菌生长中的重要作用而有助于细菌的毒力,并且具有疫苗潜力。一种假定的 TBDT,YncD,已被鉴定为伤寒人体感染过程中体内诱导的抗原之一,并且是沙门氏菌肠炎血清型 Typhi 致病性所必需的。本研究旨在确定 YncD 的功能和免疫原性。同源重组方法用于从野生型 S. Typhi Ty2 中构建 yncD 缺失突变体和 cirA-iroN-fepA 缺失突变体。在缺铁培养基中以及人巨噬细胞中评估突变体和野生型菌株的生长情况。使用 Ni-NTA 亲和层析和阴离子交换表达和纯化重组 YncD 蛋白。然后使用小鼠模型评估重组 YncD 的免疫原性和保护效力。测定抗体水平、血清杀菌效率、被动免疫保护、调理吞噬作用,以分析重组 YncD 的免疫保护机制。我们的结果表明,YncD 与 S. Typhi 的铁摄取有关。与 cirA-iroN-fepA 缺失突变体相比,yncD 缺失突变体在缺铁培养基中的生长受到损害。突变 yncD 显着降低了人巨噬细胞内细菌的生长。此外,用重组 YncD 皮下免疫小鼠可引起高水平的特异性抗-YncD IgG、IgG1 和 IgG2a,可保护免疫小鼠免受 S. Typhi 的腹腔挑战,并降低感染小鼠肝脏和脾脏中的细菌负荷。使用免疫血清进行被动免疫也有效地保护了小鼠免受 S. Typhi 的挑战。此外,免疫血清增强了补体的体外杀菌活性和调理吞噬作用。我们的结果表明,YncD 在 S. Typhi 的铁摄取中发挥作用,并且具有免疫原性。

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