烟曲霉生物膜模型中胶质毒素合成的分子特征

IF 5.9 Q1 MICROBIOLOGY
Alicia Gomez-Lopez , Candela Fernandez-Fernandez
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引用次数: 0

摘要

作为生物膜结构的菌丝生长和激活次生代谢导致低分子量分子(称为次生代谢物)的释放,是丝状真菌烟曲霉先前描述的适应和生存策略之一。我们的研究揭示了烟曲霉菌株能够在已建立的体外生物膜模型中激活与产生胶质毒素有关的机制,胶质毒素是曲霉的一种重要代谢物。胶毒素的产生表现出菌株和时间依赖性模式,并与参与其调节和合成的多个基因的表达水平相关。通过 qPCR 对其中一些基因的转录研究显示,菌株间存在时间差异,这与评估代谢物产生量时获得的结果相关。鉴于烟曲霉会在感染部位形成生物膜结构,了解胶毒素生物合成的调控可能会对曲霉感染的进化产生影响,并指导诊断和治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular characterization of gliotoxin synthesis in a biofilm model of Aspergillus fumigatus
Mycelial growth as biofilm structures and the activation of secondary metabolism leading to the release of low-molecular-weight molecules (known as secondary metabolites), are among the previously described strategies used by the filamentous fungi Aspergillus fumigatus to adapt and survive. Our study unveils that A. fumigatus strains can activate mechanisms linked to the production of gliotoxin, a crucial metabolite for Aspergillus, in the established in vitro biofilm model. Gliotoxin production exhibits strain- and time-dependent patterns and is associated -in a coordinated manner-with the expression levels of several genes involved in its regulation and synthesis. The transcriptional study of some of these genes by qPCR shows temporal inter-strain differences, which correlate with those obtained when evaluating the amounts of metabolites produced. Given that A. fumigatus forms biofilm structures within the site of infection, understanding the regulation of gliotoxin biosynthesis may have a role in the evolution of Aspergillus infection and guide diagnostic and treatment strategies.
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来源期刊
Biofilm
Biofilm MICROBIOLOGY-
CiteScore
7.50
自引率
1.50%
发文量
30
审稿时长
57 days
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