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Control of a Salmonella virulence locus by an ATP-sensing leader messenger RNA

机译:ATP传感前导信使RNA控制沙门氏菌毒力基因座。

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摘要

The facultative intracellular pathogen Salmonella enterica resides within a membrane-bound compartment inside macrophages. This compartment must be acidified for Salmonella to survive within macrophages, possibly because acidic pH promotes expression of Salmonella virulence proteins. We reasoned that Salmonella might sense its surroundings have turned acidic not only upon protonation of the extracytoplasmic domain of a protein sensor5 but also by an increase in cytosolic ATP levels, because conditions that enhance the proton gradient across the bacterial inner membrane stimulate ATP synthesis. Here we report that an increase in cytosolic ATP promotes transcription of the coding region for the virulence gene mgtC, which is the most highly induced horizontally acquired gene when Salmonella is inside macrophages. This transcript is induced both upon media acidification and by physiological conditions that increase ATP levels independently of acidification. ATP is sensed by the coupling/uncoupling of transcription of the unusually long mgtC leader messenger RNA and translation of a short open reading frame located in this region. A mutation in the mgtC leader messenger RNA that eliminates the response to ATP hinders mgtC expression inside macrophages and attenuates Salmonella virulence in mice. Our results define a singular example of an ATP-sensing leader messenger RNA. Moreover, they indicate that pathogens can interpret extracellular cues by the impact they have on cellular metabolites.
机译:兼性细胞内病原体小肠沙门氏菌位于巨噬细胞内的膜结合腔室内。为了使沙门氏菌能够在巨噬细胞中存活,必须对该隔室进行酸化处理,这可能是因为酸性pH值会促进沙门氏菌毒力蛋白的表达。我们认为沙门氏菌可能不仅感觉到蛋白质传感器胞质外域的质子化,而且还感觉到胞质ATP水平的增加,从而使周围环境变成了酸性,因为增强细菌内膜质子梯度的条件会刺激ATP的合成。在这里我们报告说,胞质ATP的增加促进了毒力基因mgtC的编码区的转录,该基因是沙门氏菌在巨噬细胞内部时诱导水平最高的基因。该转录物在培养基酸化时以及由独立于酸化而增加ATP水平的生理条件诱导。 ATP通过异常长的mgtC前导信使RNA的转录和位于该区域的短开放阅读框的翻译的偶联/解偶联来感知。 mgtC前导信使RNA中的突变消除了对ATP的反应,从而阻碍了巨噬细胞内mgtC的表达并减弱了小鼠沙门氏菌的毒力。我们的结果定义了一个ATP传感前导信使RNA的单一例子。而且,它们表明病原体可以通过它们对细胞代谢产物的影响来解释细胞外提示。

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  • 来源
    《Nature》 |2012年第7402期|p.271-275|共5页
  • 作者单位

    Howard Hughes Medical Institute, Yale School of Medicine, Section of Microbial Pathogenesis, Boyer Center for Molecular Medicine, 295 Congress Avenue, New Haven, Connecticut 06536-0812, USA,Yale Microbial Diversity Institute, P0 Box 27389, West Haven, Connecticut 06516, USA;

    Howard Hughes Medical Institute, Yale School of Medicine, Section of Microbial Pathogenesis, Boyer Center for Molecular Medicine, 295 Congress Avenue, New Haven, Connecticut 06536-0812, USA.,Yale Microbial Diversity Institute, P0 Box 27389, West Haven, Connecticut 06516, USA;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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