miRNA调控巴西副球孢子虫在铜匮乏期间的代谢适应。

IF 2.6 4区 医学 Q3 IMMUNOLOGY Microbes and Infection Pub Date : 2024-11-09 DOI:10.1016/j.micinf.2024.105435
Dener Lucas Araújo Dos Santos, Juliana Santana de Curcio, Evandro Novaes, Célia Maria de Almeida Soares
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引用次数: 0

摘要

铜是活性氧解毒、氧化磷酸化和铁吸收等细胞过程所必需的金属。然而,在感染期间,宿主会限制病原体对这种微量元素的生物利用率,以此作为一种抗感染策略。最近,我们发现在铁和锌等金属匮乏的情况下,miRNAs 参与了 P. brasiliensis 的适应性策略。然而,它们在铜限制中的作用仍有待阐明。我们的目的是描述铜缺乏时巴西蘑菇中受调控的 miRNAs 的表达谱及其可能的改变过程。通过 RNAseq 分析和生物信息学研究,我们发现了 14 个表达不同的 miRNA,其中两个可能调控氧化应激反应、β-氧化、乙醛酸循环和细胞壁重塑。我们的研究结果表明,巴西鹅膏菌在铜缺乏条件下的代谢适应受 miRNAs 的调控。
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miRNAs Regulate the Metabolic Adaptation of Paracoccidioides brasiliensis during Copper Deprivation.

Copper is an essential metal for cellular processes such as detoxification of reactive oxygen species, oxidative phosphorylation, and iron uptake. However, during infection, the host restricts the bioavailability of this micronutrient to the pathogen as a strategy to combat infection. Recently, we have shown the involvement of miRNAs as an adaptive strategy of P. brasiliensis upon metal deprivation such as iron and zinc. However, their role in copper limitation still needs to be elucidated. Our objective was to characterize the expression profile of miRNAs regulated during copper deprivation in P. brasiliensis and the putative altered processes. Through RNAseq analysis and bioinformatics, we identified 14 differentially expressed miRNAs, two of which putatively regulated oxidative stress response, beta-oxidation, glyoxylate cycle, and cell wall remodeling. Our results suggest that metabolic adaptations carried out by P. brasiliensis in copper deprivation are regulated by miRNAs.

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来源期刊
Microbes and Infection
Microbes and Infection 医学-病毒学
CiteScore
12.60
自引率
1.70%
发文量
90
审稿时长
40 days
期刊介绍: Microbes and Infection publishes 10 peer-reviewed issues per year in all fields of infection and immunity, covering the different levels of host-microbe interactions, and in particular: the molecular biology and cell biology of the crosstalk between hosts (human and model organisms) and microbes (viruses, bacteria, parasites and fungi), including molecular virulence and evasion mechanisms. the immune response to infection, including pathogenesis and host susceptibility. emerging human infectious diseases. systems immunology. molecular epidemiology/genetics of host pathogen interactions. microbiota and host "interactions". vaccine development, including novel strategies and adjuvants. Clinical studies, accounts of clinical trials and biomarker studies in infectious diseases are within the scope of the journal. Microbes and Infection publishes articles on human pathogens or pathogens of model systems. However, articles on other microbes can be published if they contribute to our understanding of basic mechanisms of host-pathogen interactions. Purely descriptive and preliminary studies are discouraged.
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