Center for Natural Science, Goucher College, Baltimore, MD, USA.
Clear Springs Foods, Inc., Research Division, Buhl, ID, USA.
Fish Shellfish Immunol. 2019 Aug;91:306-314. doi: 10.1016/j.fsi.2019.05.036. Epub 2019 May 20.
The flagellum is a complex surface structure necessary for a number of activities including motility, chemotaxis, biofilm formation and host attachment. Flagellin, the primary structural protein making up the flagellum, is an abundant and potent activator of innate and adaptive immunity and therefore expression of flagellin during infection could be deleterious to the infection process due to flagellin-mediated host recognition. Here, we use quantitative RT-PCR to demonstrate that expression of the flagellin locus fliC is repressed during the course of infection and subsequently up-regulated upon host mortality in a motile strain of Yersinia ruckeri. The kinetics of fliC repression during the infection process is relatively slow as full repression occurs 7-days after the initiation of infection and after approximately 3-logs of bacterial growth in vivo. These results suggests that Y. ruckeri possesses a regulatory system capable of sensing host and modulating the expression of motility in response. Examination of the master flagellar operon (flhDC) promoter region for evidence of transcriptional regulation and regulatory binding sites revealed potential interaction with the Rcs pathway through an Rcs(A)B Box. Deletion of rcsB (ΔrcsB) by marker-exchange mutagenesis resulted in overproduction of flagellin and unregulated motility, showing that the Rcs pathway negatively regulates biosynthesis of the flagellar apparatus. Experimental challenge with ΔrcsB and ΔrcsBΔfliC1ΔfliC2 mutants revealed that mutation of the Rcs pathway results in virulence attenuation which is dependent on presence of the flagellin gene. These results suggest that the inappropriate expression of flagellin during infection triggers host recognition and thus immune stimulation resulting in attenuation of virulence. In addition, RNAseq analyses of the ΔrcsB mutant strain verified the role of this gene as a negative regulator of the flagellar motility system and identified several additional genes regulated by the Rcs pathway.
鞭毛是一种复杂的表面结构,对于包括运动、趋化性、生物膜形成和宿主附着在内的多种活动是必需的。鞭毛蛋白是构成鞭毛的主要结构蛋白,它是先天和适应性免疫的丰富而有效的激活剂,因此,在感染过程中表达鞭毛蛋白可能会因鞭毛介导的宿主识别而对感染过程有害。在这里,我们使用定量 RT-PCR 来证明,在运动型鲁克氏耶尔森氏菌的感染过程中,鞭毛基因 flic 的表达受到抑制,随后在宿主死亡时上调。在感染过程中 flic 抑制的动力学相对较慢,因为完全抑制发生在感染开始后 7 天,并且在体内大约 3 个对数的细菌生长后。这些结果表明,鲁克氏耶尔森氏菌具有一种能够感知宿主并响应调节运动表达的调节系统。对主要鞭毛操纵子(flhDC)启动子区域进行转录调节和调节结合位点的检查表明,通过 Rcs(A)B 盒,可能与 Rcs 途径相互作用。通过标记交换诱变缺失 rcsB(ΔrcsB)导致鞭毛蛋白过度产生和不受调节的运动性,表明 Rcs 途径负调节鞭毛器的生物合成。用ΔrcsB 和ΔrcsBΔfliC1ΔfliC2 突变体进行实验性挑战表明,Rcs 途径的突变导致毒力衰减,这取决于鞭毛基因的存在。这些结果表明,在感染过程中不适当的鞭毛表达会触发宿主识别,从而引发免疫刺激,导致毒力衰减。此外,对ΔrcsB 突变株的 RNAseq 分析验证了该基因作为鞭毛运动系统负调节剂的作用,并鉴定了几个受 Rcs 途径调节的其他基因。