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长链不饱和脂肪酸传感器控制 III/VI 型分泌系统对于爱德华氏菌感染是必不可少的。

Long-chain unsaturated fatty acids sensor controlling the type III/VI secretion system is essential for Edwardsiella piscicida infection.

机构信息

State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai 200237, China.

State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai 200237, China; Shanghai Engineering Research Center of Maricultured Animal Vaccines, Shanghai, China; Laboratory of Aquatic Animal Diseases of MOA, Shanghai 200237, China.

出版信息

Microbiol Res. 2024 Aug;285:127770. doi: 10.1016/j.micres.2024.127770. Epub 2024 May 18.

Abstract

Edwardsiella piscicida is an acute marine pathogen that causes severe damage to the aquaculture industry worldwide. The pathogenesis of E. piscicida is dependent mainly on the type III secretion system (T3SS) and type VI secretion system (T6SS), both of which are critically regulated by EsrB and EsrC. In this study, we revealed that fatty acids influence T3SS expression. Unsaturated fatty acids (UFAs), but not saturated fatty acids (SFAs), directly interact with EsrC, which abolishes the function of EsrC and results in the turn-off of T3/T6SS. Moreover, during the in vivo colonization of E. piscicida, host fatty acids were observed to be transported into E. piscicida through FadL and to modulate the expression of T3/T6SS. Furthermore, the esrC mutant blocked the interaction between EsrC and UFAs, leading to dramatic growth defects in DMEM and impaired colonization in HeLa cells and zebrafish. In conclusion, this study revealed that the interaction between UFAs and EsrC to turn off T3/T6SS expression is essential for E. piscicida infection.

摘要

杀鲑爱德华氏菌是一种急性海洋病原体,可对全球水产养殖业造成严重损害。杀鲑爱德华氏菌的发病机制主要依赖于 III 型分泌系统(T3SS)和 VI 型分泌系统(T6SS),这两个系统都受到 EsrB 和 EsrC 的严格调控。在这项研究中,我们揭示了脂肪酸会影响 T3SS 的表达。不饱和脂肪酸(UFAs)而非饱和脂肪酸(SFAs)可直接与 EsrC 相互作用,从而使 EsrC 失活,导致 T3/T6SS 关闭。此外,在杀鲑爱德华氏菌的体内定植过程中,观察到宿主脂肪酸通过 FadL 被转运到杀鲑爱德华氏菌中,并调节 T3/T6SS 的表达。此外,esrC 突变体阻断了 EsrC 与 UFAs 之间的相互作用,导致 DMEM 中的生长缺陷明显,并损害了 HeLa 细胞和斑马鱼中的定植能力。总之,本研究揭示了 UFAs 与 EsrC 相互作用以关闭 T3/T6SS 表达对杀鲑爱德华氏菌感染至关重要。

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