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The fbpABC Operon Is Required for Ton-Independent Utilization of Xenosiderophores by Neisseria gonorrhoeae Strain FA19

机译:淋病奈瑟氏球菌FA19依赖吨非依赖性利用异铁载体需要fbpABC操纵子

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摘要

Neisseria gonorrhoeae produces no known siderophores but can employ host-derived, iron-binding proteins, including transferrin and lactoferrin, as iron sources. Given the propensity of this pathogen to hijack rather than synthesize iron-sequestering molecules, we hypothesized that the ability to use siderophores produced by other bacteria, or xenosiderophores, may also play a role in the survival of the gonococcus. Among a panel of diverse siderophores, only the catecholate xenosiderophores enterobactin and salmochelin promoted growth of gonococcal strain FA19. Surprisingly, the internalization pathway was independent of TonB or any of the TonB-dependent transporters. Xenosiderophore-mediated growth was similarly independent of the pilin-extruding secretin formed by PilQ and of the hydrophobic-agent efflux system composed of MtrCDE. The fbpABC operon encodes a periplasmic-binding-protein-dependent ABC transport system that enables the gonococcus to transport iron into the cell subsequent to outer membrane translocation. We hypothesized that the FbpABC proteins, required for ferric iron transport from transferrin and lactoferrin, might also contribute to the utilization of xenosiderophores as iron sources. We created mutants that conditionally expressed FbpABC from an IPTG-inducible promoter. We determined that expression of FbpABC was required for growth of gonococcal strain FA19 in the presence of enterobactin and salmochelin. The monomeric component of enterobactin, dihydroxybenzoylserine (DHBS), and the S2 form of salmochelin specifically promoted FbpABC-dependent growth of FA19. This study demonstrated that the gonococcal FbpABC transport system is required for utilization of some xenosiderophores as iron sources and that growth promotion by these ferric siderophores can occur in the absence of TonB or individual TonB-dependent transporters.
机译:淋病奈瑟氏球菌不产生已知的铁载体,但可以使用宿主来源的铁结合蛋白(包括转铁蛋白和乳铁蛋白)作为铁源。考虑到这种病原体倾向于劫持而不是合成铁螯合分子,我们假设使用其他细菌产生的铁载体或异铁载体的能力也可能在淋球菌的存活中起作用。在一组不同的铁载体中,只有儿茶酚型异铁载体Enterobactin和salmochelin促进淋球菌FA19的生长。出人意料的是,内化途径独立于TonB或任何依赖TonB的转运蛋白。异种铁载体介导的生长类似地独立于由PilQ形成的菌毛素挤出分泌素和由MtrCDE组成的疏水剂外排系统。 fbpABC操纵子编码一种依赖周质结合蛋白的ABC转运系统,该系统可使淋球菌在外膜易位后将铁转运到细胞中。我们假设从运铁蛋白和乳铁蛋白转运三价铁所需的FbpABC蛋白也可能有助于利用异铁载体作为铁源。我们创建了从IPTG诱导型启动子有条件表达FbpABC的突变体。我们确定在肠杆菌素和沙门氏菌素存在下,淋巴球菌菌株FA19的生长需要FbpABC的表达。肠杆菌素,二羟基苯甲酰丝氨酸(DHBS)和salmochelin的S2形式的单体成分特异性地促进了F19ABC依赖的FA19的生长。这项研究表明,淋球菌的FbpABC转运系统是利用某些异铁载体作为铁源所必需的,这些三价铁载体的生长促进作用可以在没有TonB或单个TonB依赖性转运子的情况下发生。

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