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Extracellular vesicle proteomes reflect developmental phases of Bacillus subtilis

机译:细胞外囊泡蛋白质体反映枯草芽孢杆菌的发育阶段

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Background: Extracellular vesicles (EV) are spherical membrane-bound vesicles with nano-scale diameters, which are shed to the extracellular region by most eukaryotic and prokaryotic cells. Bacterial EV are proposed to contribute to intercellular communication, bacterial survival and human pathogenesis as a novel secretion system. EV have been characterized from many Gram-negative species and, more recently, from several vegetative Gram-positive bacteria. Further characterization of EVand their molecular cargos will contribute to understanding bacterial physiology and to developing therapeutic approaches. Results: Bacillus subtilis were observed to release EVto a similar extent during sporulation as during the vegetative growth phase. However, the two vesicular cargos show qualitatively and quantitatively different proteomes. Among 193 total proteins identified across both samples, 61 were shown to be significantly more abundant in EV shed by sporulating cells, with (log) ratio of spectral counts Rsc > 1 and Fisher-exact test FDR < 5 %. Sixty-two proteins were found to be significantly more abundant in EVshed by vegetative cells. Membrane fusion was shown to take place between these EVs and Gram-positive cells. Conclusion: Biogenesis of EVisa continuous process over the entire life cycle of this sporulating bacterium. The formation of EV during sporulation is strongly supported by the delineation of protein content that differs from the proteome of EV formed by vegetative spores. Extracellular vesicles (EV) are universally produced from diverse eukaryotes and prokaryotes [1, 2]. They are spherical and membranous vesicles shed to the extracellular region, and enclosed by a lipid bilayer with a nano-scale diameter between 20 and 1000 nm depending on the organism [3, 4]. As in the case with EV shed by multicellular organisms, Gram-negative bacterial EV carry diverse cell-derived components, including numerous proteins, lipids, genetic materials, toxins, communication signals, and immunomodulatory compounds [4-6]. EV have been proposed to contribute to intercellular communication, bacterial survival, and human pathogenesis as a novel secretion system [1, 4-6]. Initially, Gram-positive bacteria were thought not to produce EV because they lack outer membranes. However, Gram-positive bacterial EV were microscopically observed in 1990 [7], and now EV have been characterized from several infectious Gram-positive bacteria, including S. aureus [8], B. anthracis [9], Listeria monocytogenes [10], Bacillus subtilis [11], and Clostridium perfringens [12].
机译:背景:细胞外囊泡(EV)是具有纳米级直径的球形膜结合囊泡,其通过大多数真核和原核细胞脱落到细胞外区域。提出了细菌EV,有助于细胞间通信,细菌存活和人发病,作为新的分泌系统。 EV已经从许多革兰氏阴性物质的特征,并且最近,来自几种植物革兰氏阳性细菌。 Evand的进一步表征它们的分子尸体将有助于了解细菌生理学和发展治疗方法。结果:观察枯草芽孢杆菌在培训期间释放EV至相似程度,如营养生长期。然而,两种囊泡尸体显示定性和定量不同的蛋白质素。在两个样品中鉴定的193种蛋白质中,61在孢子状细胞中显示出在EV脱落中明显更丰富,(Log)的光谱计数RSC> 1和Fisher精确测试FDR <5%。发现六十两种蛋白质被植物细胞的EVSHED显着更丰富。显示膜融合在这些EVS和革兰氏阳性细胞之间进行。结论:EVISA的生物发生在该孢子菌细菌的整个生命周期中的连续过程。通过蛋白质含量的描绘强烈地支持孢子期间EV的形成,其与由植物孢子形成的EV蛋白质组不同。细胞外囊泡(EV)普遍生产各种真核生物和原核生物[1,2]。它们是球形和膜质囊泡脱落到细胞外区域,并且由脂质双层包围,纳米级直径在20至1000nm之间,取决于生物[3,4]。如在通过多细胞生物的EV脱落的情况下,革兰氏阴性细菌EV携带不同的细胞衍生成分,包括许多蛋白质,脂质,遗传物质,毒素,通信信号和免疫调节化合物[4-6]。已经提出了导致细胞间通信,细菌存活和人性发病机构作为新的分泌系统[1,4-6]。最初,认为革兰氏阳性细菌不会产生EV,因为它们缺乏外膜。然而,1990年的革兰氏阳性细菌EV在1990年进行显微镜观察,现在EV已经表征了几种传染性革兰氏阳性细菌,包括金黄色葡萄球菌[8],B.Nethracis [9],Histeria单核细胞原[10] ,枯草芽孢杆菌[11]和梭菌性perfringens [12]。

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