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Transcriptome and proteome dynamics in chemostat culture reveal how Campylobacter jejuni modulates metabolism, stress responses and virulence factors upon changes in oxygen availability

机译:恒化器培养中的转录组和蛋白质组动态揭示了空肠弯曲杆菌如何在氧气可用性变化时调节代谢,应激反应和毒力因子

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摘要

Campylobacter jejuni, the most frequent cause of food-borne bacterial gastroenteritis worldwide, is a microaerophile that has to survive high environmental oxygen tensions, adapt to oxygen limitation in the intestine and resist host oxidative attack. Here, oxygen-dependent changes in C. jejuni physiology were studied at constant growth rate using carbon (serine)-limited continuous chemostat cultures. We show that a perceived aerobiosis scale can be calibrated by the acetate excretion flux, which becomes zero when metabolism is fully aerobic (100% aerobiosis). Transcriptome changes in a downshift experiment from 150% to 40% aerobiosis revealed many novel oxygen-regulated genes and highlighted re-modelling of the electron transport chains. A label-free proteomic analysis showed that at 40% aerobiosis, many proteins involved in host colonisation (e.g. PorA, CadF, FlpA, CjkT) became more abundant. PorA abundance increased steeply below 100% aerobiosis. In contrast, several citric-acid cycle enzymes, the peptide transporter CstA, PEB1 aspartate/glutamate transporter, LutABC lactate dehydrogenase and PutA proline dehydrogenase became more abundant with increasing aerobiosis. We also observed a co-ordinated response of oxidative stress protection enzymes and Fe-S cluster biogenesis proteins above 100% aerobiosis. Our approaches reveal key virulence factors that respond to restricted oxygen availability and specific transporters and catabolic pathways activated with increasing aerobiosis. This article is protected by copyright. All rights reserved.
机译:空肠弯曲杆菌是全世界食源性细菌性肠胃炎的最常见原因,它是一种微需氧菌,必须在高环境氧张力下生存,适应肠道中的氧气限制并抵抗宿主的氧化攻击。在这里,使用碳(丝氨酸)限制的连续化学恒温培养以恒定的生长速率研究了空肠弯曲杆菌生理中氧依赖性的变化。我们显示,可以通过乙酸排泄通量来校准感知的需氧量规模,当代谢完全有氧(100%需氧量)时,该值将为零。在从150%到40%的好氧运动降档实验中,转录组变化揭示了许多新的氧调节基因,并着重强调了电子传输链的重塑。无标记蛋白质组学分析表明,在40%的需氧量下,参与宿主定殖的许多蛋白质(例如PorA,CadF,FlpA,CjkT)变得更加丰富。在100%的需氧量以下,PorA的丰度急剧增加。相反,随着柠檬酸循环酶的增加,好氧菌增多,肽转运蛋白CstA,PEB1天冬氨酸/谷氨酸转运蛋白,LutABC乳酸脱氢酶和PutA脯氨酸脱氢酶变得更加丰富。我们还观察到氧化应激保护酶和Fe-S簇生物发生蛋白在100%需氧量以上的协调反应。我们的方法揭示了关键的毒力因子,这些因子可对有限的氧气供应以及特定的转运蛋白和分解代谢途径(随需氧量增加而激活)作出反应。本文受版权保护。版权所有。

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