College of Veterinary Medicine, Yangzhou University, Yangzhou, 225009, China.
Jiangsu Co-Innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Joint International Research Laboratory of Agriculture and Agri-Product Safety of Ministry of Education of China, Yangzhou, 225009, China.
Vet Res. 2021 Mar 10;52(1):44. doi: 10.1186/s13567-021-00915-z.
Small non-coding RNA RyhB is a key regulator of iron homeostasis in bacteria by sensing iron availability in the environment. Although RyhB is known to influence bacterial virulence by interacting with iron metabolism related regulators, its interaction with virulence genes, especially the Type III secretion system (T3SS), has not been reported. Here, we demonstrate that two RyhB paralogs of Salmonella enterica serovar Enteritidis upregulate Type III secretion system (T3SS) effectors, and consequently affect Salmonella invasion into intestinal epithelial cells. Specifically, we found that RyhB-1 modulate Salmonella response to stress condition of iron deficiency and hypoxia, and stress in simulated intestinal environment (SIE). Under SIE culture conditions, both RyhB-1 and RyhB-2 are drastically induced and directly upregulate the expression of T3SS effector gene sipA by interacting with its 5' untranslated region (5' UTR) via an incomplete base-pairing mechanism. In addition, the RyhB paralogs upregulate the expression of T3SS effector gene sopE. By regulating the invasion-related genes, RyhBs in turn affect the ability of S. Enteritidis to adhere to and invade into intestinal epithelial cells. Our findings provide evidence that RyhBs function as critical virulence factors by directly regulating virulence-related gene expression. Thus, inhibition of RyhBs may be a potential strategy to attenuate Salmonella.
小分子非编码 RNA RyhB 通过感应环境中的铁可用性来调节细菌的铁稳态,是细菌铁稳态的关键调节剂。虽然 RyhB 通过与铁代谢相关的调节剂相互作用来影响细菌的毒力,但其与毒力基因,特别是 III 型分泌系统(T3SS)的相互作用尚未报道。在这里,我们证明了肠炎沙门氏菌血清型肠炎亚种的两个 RyhB 同源物上调了 III 型分泌系统(T3SS)效应物,从而影响了沙门氏菌对肠道上皮细胞的侵袭。具体来说,我们发现 RyhB-1 调节沙门氏菌对缺铁和缺氧以及模拟肠道环境(SIE)应激条件的反应。在 SIE 培养条件下,RyhB-1 和 RyhB-2 均被强烈诱导,并通过与 SipA 基因 5'非翻译区(5'UTR)的不完全碱基配对机制直接上调其表达,从而直接上调 T3SS 效应基因 sipA 的表达。此外,RyhB 同源物上调了 T3SS 效应基因 sopE 的表达。通过调节侵袭相关基因,RyhBs 反过来影响肠炎沙门氏菌黏附和侵袭肠道上皮细胞的能力。我们的研究结果为 RyhB 作为关键毒力因子通过直接调节与毒力相关的基因表达来发挥作用提供了证据。因此,抑制 RyhB 可能是减轻沙门氏菌的一种潜在策略。