恙虫病原虫感染会减少宿主的葡萄糖生成底物,但不会减少糖酵解底物。

IF 2.9 3区 医学 Q3 IMMUNOLOGY
Infection and Immunity Pub Date : 2024-11-12 Epub Date: 2024-09-26 DOI:10.1128/iai.00284-24
Savannah E Sanchez, Travis J Chiarelli, Margaret A Park, Jason A Carlyon
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引用次数: 0

摘要

恙虫病的病原体 O. tsutsugamushi 是一种强制性细胞内细菌,它与其他立克次体一样,依赖宿主细胞中的营养物质生存,因此也依赖宿主的致病机理。根据有限的实验证据和基于基因组的硅学预测,假设恙虫病菌寄生于宿主的碳代谢中枢(CCM)。在这里,我们(重新)评估了恙虫卵对宿主细胞由葡萄糖和谷氨酰胺启动的 CCM 的依赖性。Orientia感染对宿主的葡萄糖和谷氨酰胺消耗或乳酸盐积累没有影响,这表明通过CCM的总体通量没有变化。不过,宿主细胞线粒体活性和 ATP 水平在感染期间有所降低,这与细胞内谷氨酰胺和谷氨酸池较低有关。为了进一步探究宿主 CCM 在恙虫增殖过程中的重要性,我们开发了一种用于宿主细胞培养的最小培养基,并将其与化学抑制剂搭配使用,以限制与葡萄糖和谷氨酰胺代谢相关的中间产物和过程。这些条件未能对O. tsutsugamushi的细胞内生长产生负面影响,这表明该细菌善于从宿主CCM中进行清除。因此,利用非靶向代谢组学评估了恙虫病菌感染宿主 CCM 代谢中间产物的微小变化,结果发现病原体的增殖与关键 CCM 构建模块(包括氨基酸和 TCA 循环中间产物)的减少以及脂质分解代谢的增加相对应。这项研究将恙虫病菌的增殖与宿主 CCM 的改变直接联系起来,并确定了可能对病原体健康至关重要的代谢中间产物。寄生的关键在于宿主和病原体代谢需求之间的平衡。恙虫病依赖哺乳动物宿主的生理基础仍未确定。通过评估O. tsutsugamushi增殖过程中宿主新陈代谢的变化,我们发现细菌的生长与宿主的营养环境无关,但似乎依赖于宿主的葡萄糖底物,包括氨基酸。鉴于恙虫病菌的复制对其毒力至关重要,本研究首次在后基因组时代提供了恙虫病菌可能寄生的代谢中间产物的实验证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Orientia tsutsugamushi infection reduces host gluconeogenic but not glycolytic substrates.

Orientia tsutsugamushi a causal agent of scrub typhus, is an obligate intracellular bacterium that, akin to other rickettsiae, is dependent on host cell-derived nutrients for survival and thus pathogenesis. Based on limited experimental evidence and genome-based in silico predictions, O. tsutsugamushi is hypothesized to parasitize host central carbon metabolism (CCM). Here, we (re-)evaluated O. tsutsugamushi dependency on host cell CCM as initiated by glucose and glutamine. Orientia infection had no effect on host glucose and glutamine consumption or lactate accumulation, indicating no change in overall flux through CCM. However, host cell mitochondrial activity and ATP levels were reduced during infection and correspond with lower intracellular glutamine and glutamate pools. To further probe the essentiality of host CCM in O. tsutsugamushi proliferation, we developed a minimal medium for host cell cultivation and paired it with chemical inhibitors to restrict the intermediates and processes related to glucose and glutamine metabolism. These conditions failed to negatively impact O. tsutsugamushi intracellular growth, suggesting the bacterium is adept at scavenging from host CCM. Accordingly, untargeted metabolomics was utilized to evaluate minor changes in host CCM metabolic intermediates across O. tsutsugamushi infection and revealed that pathogen proliferation corresponds with reductions in critical CCM building blocks, including amino acids and TCA cycle intermediates, as well as increases in lipid catabolism. This study directly correlates O. tsutsugamushi proliferation to alterations in host CCM and identifies metabolic intermediates that are likely critical for pathogen fitness.IMPORTANCEObligate intracellular bacterial pathogens have evolved strategies to reside and proliferate within the eukaryotic intracellular environment. At the crux of this parasitism is the balance between host and pathogen metabolic requirements. The physiological basis driving O. tsutsugamushi dependency on its mammalian host remains undefined. By evaluating alterations in host metabolism during O. tsutsugamushi proliferation, we discovered that bacterial growth is independent of the host's nutritional environment but appears dependent on host gluconeogenic substrates, including amino acids. Given that O. tsutsugamushi replication is essential for its virulence, this study provides experimental evidence for the first time in the post-genomic era of metabolic intermediates potentially parasitized by a scrub typhus agent.

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来源期刊
Infection and Immunity
Infection and Immunity 医学-传染病学
CiteScore
6.00
自引率
6.50%
发文量
268
审稿时长
3 months
期刊介绍: Infection and Immunity (IAI) provides new insights into the interactions between bacterial, fungal and parasitic pathogens and their hosts. Specific areas of interest include mechanisms of molecular pathogenesis, virulence factors, cellular microbiology, experimental models of infection, host resistance or susceptibility, and the generation of innate and adaptive immune responses. IAI also welcomes studies of the microbiome relating to host-pathogen interactions.
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