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Cyclic di-GMP-dependent Signaling Pathways in the Pathogenic Firmicute Listeria monocytogenes

机译:致病性单核细胞增生性李斯特菌中依赖循环di-GMP的信号通路

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摘要

We characterized key components and major targets of the c-di-GMP signaling pathways in the foodborne pathogen Listeria monocytogenes, identified a new c-di-GMP-inducible exopolysaccharide responsible for motility inhibition, cell aggregation, and enhanced tolerance to disinfectants and desiccation, and provided first insights into the role of c-di-GMP signaling in listerial virulence. Genome-wide genetic and biochemical analyses of c-di-GMP signaling pathways revealed that L. monocytogenes has three GGDEF domain proteins, DgcA (Lmo1911), DgcB (Lmo1912) and DgcC (Lmo2174), that possess diguanylate cyclase activity, and three EAL domain proteins, PdeB (Lmo0131), PdeC (Lmo1914) and PdeD (Lmo0111), that possess c-di-GMP phosphodiesterase activity. Deletion of all phosphodiesterase genes (ΔpdeB/C/D) or expression of a heterologous diguanylate cyclase stimulated production of a previously unknown exopolysaccharide. The synthesis of this exopolysaccharide was attributed to the pssA-E (lmo0527-0531) gene cluster. The last gene of the cluster encodes the fourth listerial GGDEF domain protein, PssE, that functions as an I-site c-di-GMP receptor essential for exopolysaccharide synthesis. The c-di-GMP-inducible exopolysaccharide causes cell aggregation in minimal medium and impairs bacterial migration in semi-solid agar, however, it does not promote biofilm formation on abiotic surfaces. The exopolysaccharide also greatly enhances bacterial tolerance to commonly used disinfectants as well as desiccation, which may contribute to survival of L. monocytogenes on contaminated food products and in food-processing facilities. The exopolysaccharide and another, as yet unknown c-di-GMP-dependent target, drastically decrease listerial invasiveness in enterocytes in vitro, and lower pathogen load in the liver and gallbladder of mice infected via an oral route, which suggests that elevated c-di-GMP levels play an overall negative role in listerial virulence.
机译:我们表征了食源性单核细胞增生李斯特氏菌李斯特菌中c-di-GMP信号通路的关键成分和主要靶标,确定了一种新的c-di-GMP诱导型胞外多糖,其可抑制运动性,细胞聚集并增强对消毒剂和干燥剂的耐受性,并提供了有关c-di-GMP信号在李斯特菌毒性中的作用的初步见解。全基因组的c-di-GMP信号通路遗传和生化分析表明,单核细胞增生李斯特氏菌具有三种GGDEF域蛋白DgcA(Lmo1911),DgcB(Lmo1912)和DgcC(Lmo2174),它们具有双鸟苷酸环化酶活性和三种EAL结构蛋白PdeB(Lmo0131),PdeC(Lmo1914)和PdeD(Lmo0111)具有c-di-GMP磷酸二酯酶活性。删除所有磷酸二酯酶基因(ΔpdeB/ C / D)或异源二鸟苷酸环化酶的表达刺激了先前未知的胞外多糖的产生。该胞外多糖的合成归因于pssA-E(lmo0527-0531)基因簇。该簇的最后一个基因编码第四个李斯特氏菌GGDEF域蛋白PssE,其功能是胞外多糖合成必不可少的I位c-di-GMP受体。 c-di-GMP诱导的胞外多糖在最小培养基中引起细胞聚集,并损害半固体琼脂中的细菌迁移,但是,它不会促进非生物表面上生物膜的形成。胞外多糖还大大提高了细菌对常用消毒剂的耐受性以及干燥能力,这可能有助于单核细胞增生李斯特菌在受污染的食品和食品加工设施中的存活。胞外多糖和另一个未知的c-di-GMP依赖性靶标,在体外显着降低了肠上皮细胞的利斯特氏菌侵袭性,并降低了经口服途径感染的小鼠肝脏和胆囊中的病原体负荷,这表明c-di升高-GMP水平在李斯特菌毒性中总体上起负面作用。

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