Institute of Preventive Veterinary Medicine, College of Veterinary Medicine of Sichuan Agricultural University, Chengdu, 611130, Sichuan, China.
Research Centre of Avian Disease, College of Veterinary Medicine of Sichuan Agricultural University, Chengdu, 611130, Sichuan, China.
Vet Res. 2021 Mar 19;52(1):48. doi: 10.1186/s13567-021-00919-9.
Iron is essential for most bacteria to survive, but excessive iron leads to damage by the Fenton reaction. Therefore, the concentration of intracellular free iron must be strictly controlled in bacteria. Riemerella anatipestifer (R. anatipestifer), a Gram-negative bacterium, encodes the iron uptake system. However, the iron homeostasis mechanism remains largely unknown. In this study, it was shown that compared with the wild type R. anatipestifer CH-1, R. anatipestifer CH-1Δfur was more sensitive to streptonigrin, and this effect was alleviated when the bacteria were cultured in iron-depleted medium, suggesting that the fur mutant led to excess iron accumulation inside cells. Similarly, compared with R. anatipestifer CH-1∆recA, R. anatipestifer CH-1∆recAΔfur was more sensitive to HO-induced oxidative stress when the bacteria were grown in iron-rich medium rather than iron-depleted medium. Accordingly, it was shown that R. anatipestifer CH-1∆recAΔfur produced more intracellular ROS than R. anatipestifer CH-1∆recA in iron-rich medium. Electrophoretic mobility shift assays showed that R. anatipestifer CH-1 Fur suppressed the transcription of putative iron uptake genes through binding to their promoter regions. Finally, it was shown that compared with the wild type, R. anatipestifer CH-1Δfur was significantly attenuated in ducklings and that the colonization ability of R. anatipestifer CH-1Δfur in various tissues or organs was decreased. All these results suggested that Fur is important for iron homeostasis in R. anatipestifer and its pathogenic mechanism.
铁对于大多数细菌的生存都是必不可少的,但过量的铁会导致 Fenton 反应造成损伤。因此,细菌必须严格控制细胞内游离铁的浓度。鸭疫里默氏杆菌(Riemerella anatipestifer,R. anatipestifer)是一种革兰氏阴性菌,编码铁摄取系统。然而,其铁稳态机制在很大程度上仍不清楚。在本研究中,与野生型 R. anatipestifer CH-1 相比,R. anatipestifer CH-1Δfur 对链黑菌素更为敏感,而当细菌在缺铁培养基中培养时,这种作用得到缓解,表明 fur 突变导致细胞内铁过量积累。同样,与 R. anatipestifer CH-1∆recA 相比,当细菌在富含铁的培养基中而不是在缺铁的培养基中生长时,R. anatipestifer CH-1∆recAΔfur 对 HO 诱导的氧化应激更为敏感。因此,结果表明,与 R. anatipestifer CH-1∆recA 相比,在富含铁的培养基中,R. anatipestifer CH-1∆recAΔfur 产生了更多的细胞内 ROS。电泳迁移率变动分析表明,R. anatipestifer CH-1 Fur 通过与启动子区域结合来抑制推定的铁摄取基因的转录。最后,与野生型相比,鸭 R. anatipestifer CH-1Δfur 在雏鸭中的毒力明显减弱,并且 R. anatipestifer CH-1Δfur 在各种组织或器官中的定植能力降低。所有这些结果表明,Fur 对于 R. anatipestifer 的铁稳态及其致病机制非常重要。