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一氧化氮通过一氧化氮传感器 HnoX 抑制发光弧菌生物膜的形成。

Nitric oxide inhibits biofilm formation by Vibrio fischeri via the nitric oxide sensor HnoX.

机构信息

Department of Microbiology and Immunology, Health Sciences Division, Loyola University Chicago, Maywood, IL, USA.

Department of Microbiology-Immunology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.

出版信息

Mol Microbiol. 2019 Jan;111(1):187-203. doi: 10.1111/mmi.14147. Epub 2018 Nov 11.

Abstract

Nitric oxide (NO) is an important defense molecule secreted by the squid Euprymna scolopes and sensed by the bacterial symbiont, Vibrio fischeri, via the NO sensor HnoX. HnoX inhibits colonization through an unknown mechanism. The genomic location of hnoX adjacent to hahK, a recently identified positive regulator of biofilm formation, suggested that HnoX may inhibit colonization by controlling biofilm formation, a key early step in colonization. Indeed, the deletion of hnoX resulted in early biofilm formation in vitro, an effect that was dependent on HahK and its putative phosphotransfer residues. An allele of hnoX that encodes a protein with increased activity severely delayed wrinkled colony formation. Control occurred at the level of transcription of the syp genes, which produce the polysaccharide matrix component. The addition of NO abrogated biofilm formation and diminished syp transcription, effects that required HnoX. Finally, an hnoX mutant formed larger symbiotic biofilms. This work has thus uncovered a host-relevant signal controlling biofilm and a mechanism for the inhibition of biofilm formation by V. fischeri. The study of V. fischeri HnoX permits us to understand not only host-associated biofilm mechanisms, but also the function of HnoX domain proteins as regulators of important bacterial processes.

摘要

一氧化氮(NO)是鱿鱼 Euprymna scolopes 分泌的一种重要防御分子,通过 NO 传感器 HnoX 被细菌共生体 Vibrio fischeri 感知。HnoX 通过未知机制抑制定植。hnoX 位于 hahK 附近,hahK 是最近鉴定的生物膜形成的正调控因子,这表明 HnoX 可能通过控制生物膜形成来抑制定植,生物膜形成是定植的关键早期步骤。事实上,hnoX 的缺失导致体外早期生物膜形成,这一效应依赖于 HahK 及其假定的磷酸转移残基。编码具有更高活性的蛋白质的 hnoX 等位基因严重延迟了皱缩菌落的形成。控制发生在产生多糖基质成分的 syp 基因的转录水平。NO 的添加消除了生物膜的形成并减少了 syp 转录,这些效应需要 HnoX。最后,hnoX 突变体形成了更大的共生生物膜。这项工作揭示了一种宿主相关信号控制生物膜形成的机制,以及 V. fischeri 抑制生物膜形成的机制。对 V. fischeri HnoX 的研究不仅使我们能够理解与宿主相关的生物膜机制,还使我们能够理解 HnoX 结构域蛋白作为重要细菌过程调节剂的功能。

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