Martin Taylor, Diaz Ignacia, Kilbourne Jacquelyn, Almarza Oscar, Segovia Cristopher, Curtiss Roy, Santander Javier
Center for Infectious Diseases and Vaccinology, The Biodesign Institute, Arizona State University, Tempe, AZ 85287, USA; School of Life and Sciences, Arizona State University, Tempe, AZ 85287, USA.
Center for Infectious Diseases and Vaccinology, The Biodesign Institute, Arizona State University, Tempe, AZ 85287, USA; Microbial Pathogenesis and Vaccinology Research Group, Faculty of Sciences, Universidad Mayor, Huechuraba 8580745, Chile.
Microb Pathog. 2016 Apr;93:204-12. doi: 10.1016/j.micpath.2016.02.020. Epub 2016 Mar 2.
The genus Edwardsiella consists of bacteria with an intrinsic resistance to cyclic cationic antimicrobial peptides (CAMPs). Edwardsiella ictaluri, a pathogen of the catfish (Ictalurus punctatus) and the causative agent of a systemic infection, is highly resistant to CAMPs. Previously, we determined that the oligo-polysaccharide (O-PS) of the lipopolysaccharide (LPS) does not play a role in the E. ictaluri CAMP resistance and an intact core-lipid A structure is necessary for CAMPs resistance. Here, we evaluated the influence of the outer-core in the CAMPs resistance and fish virulence. E. ictaluri wabG, a gene that encodes for the UDP-glucuronic acid transferase that links the lipid A-inner-core to the outer-core-oligopolysaccharides, was deleted. Deletion of ΔwabG caused a pleiotropic effect, influencing LPS synthesis, CAMPs resistance, growth, and biofilm formation. E. ictaluri ΔwabG was attenuated in zebrafish indicating the important role of LPS during fish pathogenesis. Also, we evaluated the inflammatory effects of wabG LPS in catfish ligated loop model, showing a decreased inflammatory effect at the gut level respects to the E. ictaluri wild type. We conclude that E. ictaluri CAMPs resistance is related to the molecules present in the LPS outer-core and that fish gut inflammation triggered by E. ictaluri is LPS dependent, reinforcing the hypothesis that fish gut recognizes LPS in an O-PS dependent fashion.
爱德华氏菌属的细菌对环状阳离子抗菌肽(CAMP)具有内在抗性。斑点叉尾鮰爱德华氏菌是鲶鱼(斑点叉尾鮰)的病原体和一种全身性感染的病原体,对CAMP具有高度抗性。此前,我们确定脂多糖(LPS)的寡聚多糖(O-PS)在斑点叉尾鮰爱德华氏菌对CAMP的抗性中不起作用,而完整的核心脂质A结构是对CAMP产生抗性所必需的。在此,我们评估了外核心在CAMP抗性和鱼类毒力中的影响。编码将脂质A-内核心与外核心寡聚糖连接起来的UDP-葡萄糖醛酸转移酶的斑点叉尾鮰爱德华氏菌wabG基因被删除。ΔwabG的缺失产生了多效性作用,影响LPS合成、CAMP抗性、生长和生物膜形成。斑点叉尾鮰爱德华氏菌ΔwabG在斑马鱼中减毒,表明LPS在鱼类发病机制中起重要作用。此外,我们在鲶鱼结扎肠袢模型中评估了wabG LPS的炎症效应,结果显示与斑点叉尾鮰爱德华氏菌野生型相比,其在肠道水平的炎症效应降低。我们得出结论,斑点叉尾鮰爱德华氏菌对CAMP的抗性与LPS外核心中存在的分子有关,并且斑点叉尾鮰爱德华氏菌引发的鱼类肠道炎症是LPS依赖性的,这强化了鱼类肠道以O-PS依赖性方式识别LPS的假说。