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Mycoplasmas are no exception to extracellular vesicles release: Revisiting old concepts

机译:支原体对细胞外囊泡的释放也不例外:重温旧观念

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摘要

Release of extracellular vesicles (EV) by Gram-negative and positive bacteria is being frequently reported. EV are nano-sized, membrane-derived, non-self-replicating, spherical structures shed into the extracellular environment that could play a role in bacteria-host interactions. Evidence of EV production in bacteria belonging to the class Mollicutes, which are wall-less, is mainly restricted to the genus Acholeplasma and is scanty for the Mycoplasma genus that comprises major human and animal pathogens. Here EV release by six Mycoplasma (sub)species of clinical importance was investigated. EV were obtained under nutritional stress conditions, purified by ultracentrifugation and observed by electron microscopy. The membrane proteins of EV from three different species were further identified by mass spectrometry as a preliminary approach to determining their potential role in host-pathogen interactions. EV were shown to be released by all six (sub)species although their quantities and sizes (30–220 nm) were very variable. EV purification was complicated by the minute size of viable mycoplasmal cells. The proteins of EV-membranes from three (sub)species included major components of host-pathogen interactions, suggesting that EV could contribute to make the host-pathogen interplay more complex. The process behind EV release has yet to be deciphered, although several observations demonstrated their active release from the plasma membrane of living cells. This work shed new light on old concepts of “elementary bodies” and “not-cell bound antigens”.
机译:革兰氏阴性和阳性细菌释放胞外囊泡(EV)的报道很多。 EV是落入细胞外环境的纳米级,膜源性,非自我复制的球形结构,可在细菌与宿主的相互作用中发挥作用。属于Mollicutes类且无壁的细菌中EV产生的证据主要限于Acholeplasma属,而对支原体属却缺乏,该支原体属主要的人类和动物病原体。在这里,对具有临床重要性的六个支原体(亚种)释放的EV进行了研究。 EV是在营养胁迫条件下获得的,通过超速离心纯化并通过电子显微镜观察。质谱进一步鉴定了来自三个不同物种的EV膜蛋白,作为确定其在宿主与病原体相互作用中潜在作用的初步方法。尽管所有六个(亚)物种的数量和大小(30-220 nm)变化很大,但它们均显示出EV释放。微小的活体支原体细胞使EV纯化变得复杂。来自三个亚亚种的EV膜蛋白包括宿主与病原体相互作用的主要成分,这表明EV可能有助于使宿主与病原体之间的相互作用更加复杂。 EV释放背后的过程尚未破译,尽管有几项观察表明它们是从活细胞的质膜中主动释放的。这项工作为“元素体”和“非细胞结合抗原”的旧概念提供了新的思路。

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