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铜感应转录因子 ArsR2 调节 VjbR 以维持毒力。

Copper sensing transcription factor ArsR2 regulates VjbR to sustain virulence in .

机构信息

State Key Laboratory for Animal Disease Control and Prevention, College of Veterinary Medicine, Lanzhou Veterinary Research Institute, Lanzhou University, Chinese Academy of Agricultural Sciences, Lanzhou, People's Republic of China.

Gansu Province Research Center for Basic Disciplines of Pathogen Biology, Lanzhou, People's Republic of China.

出版信息

Emerg Microbes Infect. 2024 Dec;13(1):2406274. doi: 10.1080/22221751.2024.2406274. Epub 2024 Sep 25.

Abstract

Brucellosis, caused by the intracellular pathogen , is a major zoonotic infection that promotes reproductive disease in domestic animals and chronic debilitating conditions in humans. The ArsR family of transcriptional regulators plays key roles in diverse cellular processes, including metal ion homeostasis, responding to adverse conditions, and virulence. However, little is known about the function of ArsR family members in . Here, we identified ArsR2 as a nonclassical member of the family that lacks autoregulatory function, but which nevertheless plays a vital role in maintaining copper homeostasis in . ArsR2 is a global regulator of 241 genes, including those involved in the VirB type IV secretion system (T4SS). Significantly, ArsR2 regulates T4SS production in by targeting VjbR which encodes a LuxR-type family transcriptional regulator. Moreover, copper modulates transcriptional activity of ArsR2, but not of VjbR. Furthermore, deletion of attenuated virulence in a mouse model. Collectively, these findings enhance understanding of the mechanism by which ArsR proteins regulate virulence gene expression in pathogenic species.

摘要

布鲁氏菌病是由胞内病原体引起的一种主要人畜共患病,可导致家畜生殖疾病和人类慢性虚弱。转录调节因子 ArsR 家族在多种细胞过程中发挥关键作用,包括金属离子稳态、应对不利条件和毒力。然而,人们对 ArsR 家族成员在 中的功能知之甚少。在这里,我们鉴定出 ArsR2 是该家族的一个非经典成员,它缺乏自身调节功能,但在维持 中的铜稳态中起着至关重要的作用。ArsR2 是 241 个基因的全局调节剂,包括参与 VirB 型 IV 型分泌系统 (T4SS) 的基因。重要的是,ArsR2 通过靶向编码 LuxR 型家族转录调节剂的 VjbR 来调节 T4SS 在 中的产生。此外,铜调节 ArsR2 的转录活性,但不调节 VjbR 的转录活性。此外, 缺失削弱了在小鼠模型中的毒力。总之,这些发现增强了对 ArsR 蛋白在致病性 物种中调节毒力基因表达的机制的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfcb/11425708/12971e35b025/TEMI_A_2406274_F0001_OC.jpg

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