Metformin exerts a dual effect on Mucorales virulence by altering oxidative metabolism through the regulation of rhizoferrin levels.

IF 3.5 3区 医学 Q3 INFECTIOUS DISEASES
J Alberto Patiño-Medina, Viridiana Alejandre-Castañeda, César J Torres-Cortés, León Francisco Ruíz-Herrera, Marco I Valle-Maldonado, César R Solorio-Alvarado, Joel Ramírez-Emiliano, Karla Viridiana Castro-Cerritos, Rafael Ortíz-Alvarado, Francisco E Nicolas, Victoriano Garre, Martha I Ramírez-Díaz, Ulrike Binder, Víctor Meza-Carmen
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引用次数: 0

Abstract

Mucormycosis, caused by fungi belonging to the order Mucorales, is associated with patients who suffer from uncontrolled diabetes mellitus. Blood glucose management in diabetic patients is performed through multiple strategies, with metformin being a common drug for controlling these levels. In this work, we show that the addition of low or high concentrations of metformin during the culture of Mucor lusitanicus and Rhizopus arrhizus differentially affects the toxicity of their cell-free culture supernatants toward Caenorhabditis elegans. The same effect was observed in infections of Galleria mellonella and mice treated with different metformin concentrations. Virulence induced by low concentrations of metformin correlates with augmented mitochondrial activity, which enhances respiration and increases hydroxyl radical (•OH) levels. Moreover, the SS toxicity towards C. elegans was eliminated by a mitophagy inducer and oxidative metabolism inhibitors, supporting that the effect of low metformin concentration on virulence is mediated by enhancing mitochondrial activity. Meanwhile, high metformin concentrations led to decreased virulence and reduced mitochondrial activity, along with the upregulation of AMP-activated protein kinase (AMPK)-α1-subunit (known also as Snfα-1), a mitophagy marker, catalase, and superoxide dismutase transcripts. Furthermore, deletion of the genes encoding the regulatory subunit of protein kinase A (PkaR1) and rhizoferrin synthetase partially revealed the signaling pathway underlying metformin-induced virulence of M. lusitanicus. In general, we found that metformin concentrations have a dual effect on the virulence of both Mucorales species by regulating oxidative metabolism, which may be relevant to the outcome of mucormycosis in diabetic patients treated with metformin.

二甲双胍通过调节根铁蛋白水平改变氧化代谢,对毛霉毒力产生双重影响。
毛霉菌病是由属于毛霉菌目的真菌引起的,与糖尿病不受控制的患者有关。糖尿病患者的血糖管理通过多种策略进行,二甲双胍是控制血糖水平的常用药物。在本研究中,我们发现在lusitanicus和arrhizopus的培养过程中添加低浓度或高浓度的二甲双胍会对其无细胞培养上清(SS)对秀丽隐杆线虫的毒性产生不同的影响。用不同二甲双胍浓度处理的小鼠和受mellonella感染的小鼠也观察到同样的效果。低浓度二甲双胍诱导的毒力与线粒体活性增强相关,线粒体活性增强呼吸作用并增加羟基自由基(•OH)水平。此外,SS对秀丽隐杆线虫的毒性被线粒体自噬诱导剂和氧化代谢抑制剂消除,支持低二甲双胍浓度对毒力的影响是通过增强线粒体活性介导的。同时,高浓度二甲双胍导致毒力下降和线粒体活性降低,同时amp活化的蛋白激酶(AMPK)-α1亚基(也称为Snfα-1)、线粒体自噬标记物、过氧化氢酶和超氧化物歧化酶转录物上调。此外,编码蛋白激酶A (PkaR1)和根铁蛋白合成酶调控亚基的基因的缺失部分揭示了二甲双胍诱导的lusitanicus毒力的信号通路。总的来说,我们发现二甲双胍浓度通过调节氧化代谢对两种毛霉菌的毒力有双重影响,这可能与二甲双胍治疗的糖尿病患者毛霉菌病的结局有关。
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来源期刊
Medical mycology
Medical mycology 医学-兽医学
CiteScore
5.70
自引率
3.40%
发文量
632
审稿时长
12 months
期刊介绍: Medical Mycology is a peer-reviewed international journal that focuses on original and innovative basic and applied studies, as well as learned reviews on all aspects of medical, veterinary and environmental mycology as related to disease. The objective is to present the highest quality scientific reports from throughout the world on divergent topics. These topics include the phylogeny of fungal pathogens, epidemiology and public health mycology themes, new approaches in the diagnosis and treatment of mycoses including clinical trials and guidelines, pharmacology and antifungal susceptibilities, changes in taxonomy, description of new or unusual fungi associated with human or animal disease, immunology of fungal infections, vaccinology for prevention of fungal infections, pathogenesis and virulence, and the molecular biology of pathogenic fungi in vitro and in vivo, including genomics, transcriptomics, metabolomics, and proteomics. Case reports are no longer accepted. In addition, studies of natural products showing inhibitory activity against pathogenic fungi are not accepted without chemical characterization and identification of the compounds responsible for the inhibitory activity.
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