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黄曲霉分离株特异性响应氧化应激与黄曲霉毒素生产能力关系的蛋白质组分析。

Proteome analysis of Aspergillus flavus isolate-specific responses to oxidative stress in relationship to aflatoxin production capability.

机构信息

Department of Plant Pathology, University of Georgia, Tifton, GA, USA.

USDA-ARS Crop Protection and Management Research Unit, Tifton, GA, USA.

出版信息

Sci Rep. 2018 Feb 21;8(1):3430. doi: 10.1038/s41598-018-21653-x.

Abstract

Aspergillus flavus is an opportunistic pathogen of plants such as maize and peanut under conducive conditions such as drought stress resulting in significant aflatoxin production. Drought-associated oxidative stress also exacerbates aflatoxin production by A. flavus. The objectives of this study were to use proteomics to provide insights into the pathogen responses to HO-derived oxidative stress, and to identify potential biomarkers and targets for host resistance breeding. Three isolates, AF13, NRRL3357, and K54A with high, moderate, and no aflatoxin production, were cultured in medium supplemented with varying levels of HO, and examined using an iTRAQ (Isobaric Tags for Relative and Absolute Quantification) approach. Overall, 1,173 proteins were identified and 220 were differentially expressed (DEPs). Observed DEPs encompassed metabolic pathways including antioxidants, carbohydrates, pathogenicity, and secondary metabolism. Increased lytic enzyme, secondary metabolite, and developmental pathway expression in AF13 was correlated with oxidative stress tolerance, likely assisting in plant infection and microbial competition. Elevated expression of energy and cellular component production in NRRL3357 and K54A implies a focus on oxidative damage remediation. These trends explain isolate-to-isolate variation in oxidative stress tolerance and provide insights into mechanisms relevant to host plant interactions under drought stress allowing for more targeted efforts in host resistance research.

摘要

黄曲霉是一种机会性病原体,在干旱等有利条件下会导致玉米和花生等植物产生大量黄曲霉毒素。与干旱相关的氧化应激也会加剧黄曲霉产生黄曲霉毒素。本研究的目的是利用蛋白质组学深入了解病原体对 HO 衍生的氧化应激的反应,并鉴定潜在的生物标志物和宿主抗性育种的靶标。使用 iTRAQ(Isobaric Tags for Relative and Absolute Quantification)方法,对具有高、中、低黄曲霉毒素产量的三个分离株 AF13、NRRL3357 和 K54A 在不同 HO 水平的培养基中进行培养,并进行了检测。总的来说,鉴定了 1173 种蛋白质,其中 220 种表达差异(DEPs)。观察到的 DEPs 涵盖了代谢途径,包括抗氧化剂、碳水化合物、致病性和次生代谢。AF13 中溶酶体酶、次生代谢物和发育途径表达的增加与氧化应激耐受性相关,可能有助于植物感染和微生物竞争。NRRL3357 和 K54A 中能量和细胞成分产生的表达增加表明其专注于氧化损伤修复。这些趋势解释了不同分离株间氧化应激耐受性的差异,并为干旱胁迫下与宿主植物相互作用相关的机制提供了深入了解,从而使宿主抗性研究更有针对性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5059/5821837/d068dda85a58/41598_2018_21653_Fig1_HTML.jpg

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