Department of Biosciences, University of Oslo, 0316, Oslo, Norway.
Department of Molecular Microbiology and Institute of Biomembranes, Utrecht University, Utrecht, The Netherlands.
Environ Microbiol. 2020 Jul;22(7):2939-2955. doi: 10.1111/1462-2920.15051. Epub 2020 May 17.
Yersinia ruckeri causes enteric redmouth disease (ERM) that mainly affects salmonid fishes and leads to significant economic losses in the aquaculture industry. An increasing number of outbreaks and the lack of effective vaccines against some serotypes necessitates novel measures to control ERM. Importantly, Y. ruckeri survives in the environment for long periods, presumably by forming biofilms. How the pathogen forms biofilms and which molecular factors are involved in this process, remains unclear. Yersinia ruckeri produces two surface-exposed adhesins, belonging to the inverse autotransporters (IATs), called Y. ruckeri invasin (YrInv) and Y. ruckeri invasin-like molecule (YrIlm). Here, we investigated whether YrInv and YrIlm play a role in biofilm formation and virulence. Functional assays revealed that YrInv and YrIlm promote biofilm formation on different abiotic substrates. Confocal microscopy revealed that they are involved in microcolony interaction and formation, respectively. The effect of both IATs on biofilm formation correlated with the presence of different biopolymers in the biofilm matrix, including extracellular DNA, RNA and proteins. Moreover, YrInv and YrIlm contributed to virulence in the Galleria mellonella infection model. Taken together, we propose that both IATs are possible targets for the development of novel diagnostic and preventative strategies to control ERM.
鲁氏耶尔森菌引起的肠型红嘴病(ERM)主要影响鲑鱼科鱼类,并导致水产养殖业的重大经济损失。越来越多的疫情爆发和某些血清型缺乏有效的疫苗,需要采取新的措施来控制 ERM。重要的是,鲁氏耶尔森菌在环境中能长时间存活,可能是通过形成生物膜。该病原体如何形成生物膜以及该过程涉及哪些分子因素尚不清楚。鲁氏耶尔森菌产生两种表面暴露的黏附素,属于反向自转运体(IAT),分别称为鲁氏耶尔森菌侵袭素(YrInv)和鲁氏耶尔森菌侵袭素样分子(YrIlm)。在这里,我们研究了 YrInv 和 YrIlm 是否在生物膜形成和毒力中发挥作用。功能分析显示,YrInv 和 YrIlm 促进了不同非生物基质上生物膜的形成。共聚焦显微镜显示,它们分别参与了微菌落的相互作用和形成。两种 IAT 对生物膜形成的影响与生物膜基质中不同生物聚合物的存在相关,包括胞外 DNA、RNA 和蛋白质。此外,YrInv 和 YrIlm 有助于在大蜡螟感染模型中的毒力。综上所述,我们提出这两种 IAT 可能是开发新型诊断和预防策略来控制 ERM 的潜在靶点。