Chytridiomycosis disrupts metabolic responses in amphibians at metamorphic climax.

IF 2.6 4区 医学 Q3 IMMUNOLOGY Microbes and Infection Pub Date : 2024-11-15 DOI:10.1016/j.micinf.2024.105438
Josephine E Humphries, Steven D Melvin, Chantal Lanctôt, Hamish McCallum, David Newell, Laura F Grogan
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Abstract

The fungal disease chytridiomycosis (causative agent Batrachochytrium dendrobatidis [Bd]) is a primary contributor to amphibian species declines. The morphological and physiological reorganization that occurs during amphibian metamorphosis likely increases the vulnerability of metamorphs to Bd. To address this, we exposed pro-metamorphic tadpoles of Fleay's barred frog (Mixophyes fleayi) to Bd and sampled skin and liver sections from control and exposed animals throughout metamorphosis (Gosner stages 40, 42 and 45). We used an untargeted metabolomics approach to assess the metabolic impacts of Bd infection during the critical metamorphic stages, extracting metabolites from sampled tissues and analysing them via Nuclear Magnetic Resonance spectrometry. Most exposed animals became moribund at Gosner stage 45, while a subset seemingly cleared their infections. Metabolite abundance varied throughout development, with Gosner stage 45 samples distinct from previous stages. Clinically infected animals at Gosner stage 45 exhibited profound metabolic dysregulation (e.g., upregulation of amino acid biosynthesis and degradation) in comparison to uninfected groups (negative controls and 'cleared' animals). Despite showing parallels with previous metabolomic analyses of Bd-infected adult frogs, we identified variations in our results that could be attributed to the dramatic changes that characterise metamorphosis and may be driving the heightened vulnerability observed in metamorphic amphibians.

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恙虫病扰乱了处于变态高潮期的两栖动物的新陈代谢反应。
真菌病糜烂性真菌病(病原体为蝙蝠疫[Bd])是造成两栖动物物种减少的主要原因。两栖动物变态过程中发生的形态和生理重组可能会增加变态者对 Bd 的易感性。为了解决这个问题,我们将弗莱氏条纹蛙(Mixophyes fleayi)的原变态蝌蚪暴露于 Bd,并在整个变态过程(Gosner 阶段 40、42 和 45)中对对照组和暴露组动物的皮肤和肝脏切片进行取样。我们采用非靶向代谢组学方法来评估 Bd 感染在关键变态阶段对代谢的影响,从取样组织中提取代谢物,并通过核磁共振光谱法进行分析。大多数受感染的动物在戈斯纳第 45 阶段奄奄一息,而一部分动物似乎清除了感染。代谢物丰度在整个发育过程中各不相同,Gosner 第 45 阶段的样本与之前的阶段截然不同。与未感染组(阴性对照组和 "清除 "动物)相比,临床感染动物在 Gosner 45 阶段表现出严重的代谢失调(如氨基酸生物合成和降解的上调)。尽管与之前对受 Bd 感染的成年蛙进行的代谢组学分析结果相似,但我们发现我们的研究结果存在差异,这些差异可能是由于变态过程中发生的巨大变化造成的,也可能是导致变态两栖动物更易受伤害的原因。
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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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