The role of l-serine and l-threonine in the energy metabolism and nutritional stress response of Trypanosoma cruzi.

IF 3.7 2区 生物学 Q2 MICROBIOLOGY
mSphere Pub Date : 2025-03-25 Epub Date: 2025-03-05 DOI:10.1128/msphere.00983-24
Mayke Bezerra Alencar, Richard Marcel Bruno Moreira Girard, Marcell Crispim, Carlos Gustavo Baptista, Marc Biran, Frederic Bringaud, Ariel Mariano Silber
{"title":"The role of l-serine and l-threonine in the energy metabolism and nutritional stress response of <i>Trypanosoma cruzi</i>.","authors":"Mayke Bezerra Alencar, Richard Marcel Bruno Moreira Girard, Marcell Crispim, Carlos Gustavo Baptista, Marc Biran, Frederic Bringaud, Ariel Mariano Silber","doi":"10.1128/msphere.00983-24","DOIUrl":null,"url":null,"abstract":"<p><p>l-Serine and l-threonine have versatile roles in metabolism. In addition to their use in protein synthesis, these amino acids participate in the biosynthesis pathways of other amino acids and even phospholipids. Furthermore, l-serine and l-threonine can be substrates for a serine/threonine dehydratase (Ser/ThrDH), resulting in pyruvate and 2-oxobutyrate, respectively, thus being amino acids with anaplerotic potential. <i>Trypanosoma cruzi</i>, the etiological agent of Chagas disease, uses amino acids in several biological processes: metacyclogenesis, infection, resistance to nutritional and oxidative stress, osmotic control, etc. This study investigated the import and metabolism of l-serine, l-threonine, and glycine in <i>T. cruzi</i>. Our results demonstrate that these amino acids are transported from the extracellular environment into <i>T. cruzi</i> cells through a saturable transport system that fits the Michaelis-Menten model. Our results show that l-serine and l-threonine can sustain epimastigote cell viability under nutritional stress conditions and stimulate oxygen consumption, maintaining intracellular ATP levels. Additionally, our findings indicate that serine plays a role in establishing the mitochondrial membrane potential in <i>T. cruzi</i>. Serine is also involved in energy metabolism via the serine-pyruvate pathway, which stimulates the production and subsequent excretion of acetate and alanine. Our results demonstrate the importance of l-serine and l-threonine in the energy metabolism of <i>T. cruzi</i> and provide new insights into the metabolic adaptations of this parasite during its life cycle.IMPORTANCE<i>Trypanosoma cruzi</i>, the parasite responsible for Chagas disease, impacts 5-6 million individuals in the Americas and is rapidly spreading globally due to significant human migration. This parasitic organism undergoes a complex life cycle involving triatomine insects and mammalian hosts, thriving in diverse environments, such as various regions within the insect's digestive tract and mammalian cell cytoplasm. Crucially, its transmission hinges on its adaptive capabilities to varying environments. One of the most challenging environments is the insect's digestive tract, marked by nutrient scarcity between blood meals, redox imbalance, and osmotic stresses induced by the triatomine's metabolism. To endure these conditions, <i>T. cruzi</i> has developed a remarkably versatile metabolic network enabling it to metabolize sugars, lipids, and amino acids efficiently. However, the full extent of metabolites this parasite can thrive on remains incompletely understood. This study reveals that, beyond conventional carbon and energy sources (glucose, palmitic acids, proline, histidine, glutamine, and alanine), three additional metabolites (serine, threonine, and glycine) play vital roles in the parasite's survival during starvation. Remarkably, serine and threonine directly contribute to ATP production through a serine/threonine dehydratase enzyme not previously described in <i>T. cruzi</i>. The significance of this metabolic pathway for the parasite's survival sheds light on how metabolic networks aid in its endurance under extreme conditions and its ability to thrive in diverse metabolic settings.</p>","PeriodicalId":19052,"journal":{"name":"mSphere","volume":" ","pages":"e0098324"},"PeriodicalIF":3.7000,"publicationDate":"2025-03-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11934319/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"mSphere","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1128/msphere.00983-24","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/3/5 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

l-Serine and l-threonine have versatile roles in metabolism. In addition to their use in protein synthesis, these amino acids participate in the biosynthesis pathways of other amino acids and even phospholipids. Furthermore, l-serine and l-threonine can be substrates for a serine/threonine dehydratase (Ser/ThrDH), resulting in pyruvate and 2-oxobutyrate, respectively, thus being amino acids with anaplerotic potential. Trypanosoma cruzi, the etiological agent of Chagas disease, uses amino acids in several biological processes: metacyclogenesis, infection, resistance to nutritional and oxidative stress, osmotic control, etc. This study investigated the import and metabolism of l-serine, l-threonine, and glycine in T. cruzi. Our results demonstrate that these amino acids are transported from the extracellular environment into T. cruzi cells through a saturable transport system that fits the Michaelis-Menten model. Our results show that l-serine and l-threonine can sustain epimastigote cell viability under nutritional stress conditions and stimulate oxygen consumption, maintaining intracellular ATP levels. Additionally, our findings indicate that serine plays a role in establishing the mitochondrial membrane potential in T. cruzi. Serine is also involved in energy metabolism via the serine-pyruvate pathway, which stimulates the production and subsequent excretion of acetate and alanine. Our results demonstrate the importance of l-serine and l-threonine in the energy metabolism of T. cruzi and provide new insights into the metabolic adaptations of this parasite during its life cycle.IMPORTANCETrypanosoma cruzi, the parasite responsible for Chagas disease, impacts 5-6 million individuals in the Americas and is rapidly spreading globally due to significant human migration. This parasitic organism undergoes a complex life cycle involving triatomine insects and mammalian hosts, thriving in diverse environments, such as various regions within the insect's digestive tract and mammalian cell cytoplasm. Crucially, its transmission hinges on its adaptive capabilities to varying environments. One of the most challenging environments is the insect's digestive tract, marked by nutrient scarcity between blood meals, redox imbalance, and osmotic stresses induced by the triatomine's metabolism. To endure these conditions, T. cruzi has developed a remarkably versatile metabolic network enabling it to metabolize sugars, lipids, and amino acids efficiently. However, the full extent of metabolites this parasite can thrive on remains incompletely understood. This study reveals that, beyond conventional carbon and energy sources (glucose, palmitic acids, proline, histidine, glutamine, and alanine), three additional metabolites (serine, threonine, and glycine) play vital roles in the parasite's survival during starvation. Remarkably, serine and threonine directly contribute to ATP production through a serine/threonine dehydratase enzyme not previously described in T. cruzi. The significance of this metabolic pathway for the parasite's survival sheds light on how metabolic networks aid in its endurance under extreme conditions and its ability to thrive in diverse metabolic settings.

l-丝氨酸和l-苏氨酸在克氏锥虫能量代谢和营养应激反应中的作用。
l-丝氨酸和l-苏氨酸在新陈代谢中有多种作用。除了用于蛋白质合成外,这些氨基酸还参与其他氨基酸甚至磷脂的生物合成途径。此外,l-丝氨酸和l-苏氨酸可以作为丝氨酸/苏氨酸脱水酶(Ser/ThrDH)的底物,分别产生丙酮酸和2-氧丁酸,因此是具有复变潜力的氨基酸。恰加斯病的病原克氏锥虫在几个生物过程中使用氨基酸:元胞形成、感染、抵抗营养和氧化应激、渗透控制等。本研究研究了克氏体中l-丝氨酸、l-苏氨酸和甘氨酸的输入和代谢。我们的研究结果表明,这些氨基酸通过符合Michaelis-Menten模型的饱和运输系统从细胞外环境运输到T. cruzi细胞。我们的研究结果表明,l-丝氨酸和l-苏氨酸可以在营养胁迫条件下维持嗜马鞭毛细胞的活力,刺激氧气消耗,维持细胞内ATP水平。此外,我们的研究结果表明丝氨酸在克氏体线粒体膜电位的建立中起作用。丝氨酸还通过丝氨酸-丙酮酸途径参与能量代谢,刺激乙酸和丙氨酸的产生和随后的排泄。我们的研究结果证明了l-丝氨酸和l-苏氨酸在克氏锥虫能量代谢中的重要性,并为克氏锥虫在其生命周期中的代谢适应提供了新的见解。克氏斑虫是导致恰加斯病的寄生虫,在美洲影响着500万至600万人,由于大量人类迁徙,克氏斑虫正在全球迅速蔓延。这种寄生生物经历了一个复杂的生命周期,涉及triatomine昆虫和哺乳动物宿主,在不同的环境中茁壮成长,例如昆虫消化道和哺乳动物细胞质的不同区域。至关重要的是,它的传播取决于它对不同环境的适应能力。最具挑战性的环境之一是昆虫的消化道,其特征是血餐之间的营养缺乏,氧化还原失衡,以及由triatomine代谢引起的渗透应激。为了忍受这些条件,克氏T. cruzi发展了一个非常通用的代谢网络,使它能够有效地代谢糖、脂质和氨基酸。然而,这种寄生虫赖以生存的代谢物的全部范围仍不完全清楚。这项研究表明,除了传统的碳和能量来源(葡萄糖、棕榈酸、脯氨酸、组氨酸、谷氨酰胺和丙氨酸)外,另外三种代谢物(丝氨酸、苏氨酸和甘氨酸)在寄生虫饥饿期间的生存中起着至关重要的作用。值得注意的是,丝氨酸和苏氨酸通过一种丝氨酸/苏氨酸脱水酶直接促进ATP的产生,这种酶在克氏锥虫中没有被描述过。这种代谢途径对寄生虫生存的重要性揭示了代谢网络如何帮助其在极端条件下的耐力和在各种代谢环境中茁壮成长的能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
mSphere
mSphere Immunology and Microbiology-Microbiology
CiteScore
8.50
自引率
2.10%
发文量
192
审稿时长
11 weeks
期刊介绍: mSphere™ is a multi-disciplinary open-access journal that will focus on rapid publication of fundamental contributions to our understanding of microbiology. Its scope will reflect the immense range of fields within the microbial sciences, creating new opportunities for researchers to share findings that are transforming our understanding of human health and disease, ecosystems, neuroscience, agriculture, energy production, climate change, evolution, biogeochemical cycling, and food and drug production. Submissions will be encouraged of all high-quality work that makes fundamental contributions to our understanding of microbiology. mSphere™ will provide streamlined decisions, while carrying on ASM''s tradition for rigorous peer review.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信