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解析SPD_0739的全面影响:铁稳态中的关键效应器

Unraveling the full impact of SPD_0739: a key effector in iron homeostasis.

作者信息

Womack Edroyal, Antone Melina, Eichenbaum Zehava

机构信息

Department of Biology, Georgia State University, Atlanta, Georgia, USA.

出版信息

Microbiol Spectr. 2024 Oct 29;12(12):e0133124. doi: 10.1128/spectrum.01331-24.

Abstract

UNLABELLED

is a common member of the nasopharynx commensal microflora and the leading etiological agent of bacterial pneumonia in young children and aging adults. SPD_0739, a highly expressed lipoprotein, is the predicted substrate-binding component of an ABC transporter linked to the uptake of nucleosides and heme by independent studies (named PnrA or Spbhp-37, respectively). Here, we demonstrate that SPD_0739 binds heme and contributes to the bacterial binding to hemoglobin. A ∆ strain exhibited growth attenuation that was relieved by the inactivation of the transporter. Knocking out in the wild type, or the Δ strain resulted in heme accumulation, higher sensitivity to heme toxicity, and a small growth reduction compared to medium supplemented with a nucleoside mixture. In addition, loss results in higher iron- and heme-related gene expression and lower HO production. Altogether, the data are consistent with a role in nucleoside import and show that SPD_0739 does not import heme. Instead, it indirectly influences iron and heme metabolism, linking nucleosides and iron status in e.

IMPORTANCE

obtains growth essential iron from hemoglobin and other host hemoproteins. Still, the bacterial mechanisms involved are only partially understood, and there are inconsistent reports regarding the function of several transporters implicated in iron uptake. In this study, we clarified the role of PnrA/Spbhp-37, a ligand-binding protein previously linked to nucleoside or heme by different studies. We present data supporting a role in nucleoside scavenging rather than heme import and reveal that PnrA/Spbhp-37 modulates iron and heme uptake, likely by influencing the nucleoside cellular pool. Hence, this work provides a new understanding of a process critical to the pathophysiology of a significant human pathogen. Moreover, PnrA/Spbhp-37 is an abundant and immunogenic surface protein that is highly conserved. Hence, this study also clarifies the function of a promising vaccine target.

摘要

未标记

是鼻咽部共生微生物群的常见成员,也是幼儿和老年人细菌性肺炎的主要病原体。SPD_0739是一种高表达脂蛋白,经独立研究预测它是一种ABC转运蛋白的底物结合成分,与核苷和血红素的摄取有关(分别命名为PnrA或Spbhp - 37)。在此,我们证明SPD_0739结合血红素并有助于细菌与血红蛋白结合。一个∆菌株表现出生长衰减,而转运蛋白的失活可缓解这种衰减。在野生型或∆菌株中敲除会导致血红素积累、对血红素毒性的更高敏感性,并且与补充核苷混合物的培养基相比生长略有降低。此外,缺失会导致与铁和血红素相关的基因表达升高以及HO产生降低。总体而言,这些数据与在核苷导入中的作用一致,并表明SPD_0739不导入血红素。相反,它间接影响铁和血红素代谢,将核苷与大肠杆菌中的铁状态联系起来。

重要性

从血红蛋白和其他宿主血红素蛋白中获取生长必需的铁。然而,所涉及的细菌机制仅被部分理解,并且关于几种参与铁摄取的转运蛋白的功能存在不一致的报道。在本研究中,我们阐明了PnrA/Spbhp - 37的作用,一种先前在不同研究中与核苷或血红素相关的配体结合蛋白。我们提供的数据支持其在核苷清除而非血红素导入中的作用,并揭示PnrA/Spbhp - 37调节铁和血红素摄取,可能是通过影响核苷细胞池。因此,这项工作为对一种重要人类病原体病理生理学至关重要的过程提供了新的理解。此外,PnrA/Spbhp - 37是一种丰富且具有免疫原性的表面蛋白,高度保守。因此,本研究也阐明了一个有前景的疫苗靶点的功能。

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