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The role of flagella and chemotaxis genes in host pathogen interaction of the host adapted Salmonella enterica serovar Dublin compared to the broad host range serovar S. Typhimurium

机译:与宿主范围广泛的鼠伤寒沙门氏菌相比,鞭毛和趋化性基因在宿主适应性沙门氏菌血清都柏林的宿主病原体相互作用中的作用

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摘要

BackgroundThe importance of flagella and chemotaxis genes in host pathogen interaction in Salmonella enterica is mainly based on studies of the broad host range serovar, S. Typhimurium, while little is known on the importance in host specific and host adapted serovars, such as S. Dublin. In the current study we have used previously characterized insertion mutants in flagella and chemotaxis genes to investigate this and possible differences in the importance between the two serovars.ResultsfliC (encoding the structural protein of the flagella) was essential for adhesion and fliC and cheB (CheB restores the chemotaxis system to pre-stimulus conformation) were essential for invasion of S. Dublin into epithelial Int407 cells. In S. Typhimurium, both lack of flagella (fliC/fljB double mutant) and cheB influenced adhesion, and invasion was influenced by lack of both cheA (the histidine-kinase of the chemotaxis system), fliC/fljB and cheB mutation. Uptake in J774A.1 macrophage cells was significantly reduced in cheA, cheB and fliC mutants of S. Dublin, while cheA was dispensable in S. Typhimurium. Removal of flagella in both serotypes caused an increased ability to propagate intracellular in J774 macrophage cells and decreased cytotoxicity toward these cells. Flagella and chemotaxis genes were found not to influence the oxidative response. The induction of IL-6 from J774A-1 cells depended on the presence of flagella in S. Typhimurium, whilst this was not the case following challenge with S. Dublin. Addition of fliC from S. Typhimurium in trans to a fliC mutant of S. Dublin increased cytotoxicity but it did not increase the IL-6 production. Flagella were demonstrated to contribute to the outcome of infection following oral challenge of mice in S. Dublin, while an S. Typhimurium fliC/fljB mutant showed increased virulence following intra peritoneal challenge.ConclusionsThe results showed that flagella and chemotaxis genes differed in their role in host pathogen interaction between S. Dublin and S. Typhimurium. Notably, lack of flagella conferred a more virulent phenotype in S. Typhimurium at systemic sites, while this was not the case in S. Dublin. In vitro assays suggested that this could be related to flagella-induced induction of the IL-6 pro-inflammatory response, but further in vivo studies are needed to confirm this.
机译:背景鞭毛和趋化基因在肠沙门氏菌宿主病原体相互作用中的重要性主要是基于对广泛的宿主血清型鼠伤寒沙门氏菌的研究,而对于宿主特异性和适应宿主的血清型(如都柏林沙门氏菌)的重要性了解甚少。 。在当前的研究中,我们使用了先前表征的鞭毛和趋化性基因的插入突变体来研究这种情况以及两种血清型之间重要性的可能差异。结果fliC(编码鞭毛的结构蛋白)对于黏附以及fliC和cheB(CheB)是必不可少的恢复趋化系统至刺激前的构象)对于都柏林链球菌侵入上皮Int407细胞至关重要。在鼠伤寒沙门氏菌中,鞭毛(fliC / fljB双突变体)和cheB的缺乏都会影响粘连,而cheA(化学趋化系统的组氨酸激酶),fliC / fljB和cheB突变均会影响侵袭。在CheA,cheB和fliC突变体的都柏林链球菌中,J774A.1巨噬细胞的摄取显着降低,而在鼠伤寒沙门氏菌中,cheA是可有可无的。去除两种血清型中的鞭毛均导致J774巨噬细胞在细胞内繁殖的能力增强,并且对这些细胞的细胞毒性降低。发现鞭毛和趋化性基因不影响氧化反应。来自J774A-1细胞的IL-6的诱导取决于鼠伤寒沙门氏菌中鞭毛的存在,而用都柏林链球菌攻击却并非如此。将来自鼠伤寒沙门氏菌的fliC反式添加到都柏林沙门氏菌的fliC突变体中,增加了细胞毒性,但并未增加IL-6的产生。鞭毛被证明对都柏林沙门氏菌小鼠口服攻击后的感染结果有贡献,而鼠伤寒沙门氏菌fliC / fljB突变体在腹膜内攻击后显示出更高的毒力。结论结果表明,鞭毛和趋化性基因的作用不同病原菌在都柏林链霉菌和鼠伤寒沙门氏菌之间的相互作用。值得注意的是,鞭毛的缺乏使系统性部位的鼠伤寒沙门氏菌具有更强的表型,而都柏林沙门氏菌则并非如此。体外试验表明,这可能与鞭毛诱导的IL-6促炎反应有关,但需要进一步的体内研究来证实这一点。

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