{"title":"Transcriptomic Analysis Reveals Mechanisms Underlying the Inhibitory Effects of (E)-2-Heptenal on Spore Germination of Aspergillus Flavus","authors":"Jing Ren, Wen-Yan Duan, Yi-Wen Feng, Shuai-Bing Zhang, Yang-Yong Lv, Huan-Chen Zhai, Shan Wei, Ping-An Ma, Yuan-Sen Hu","doi":"10.1007/s11483-024-09868-0","DOIUrl":null,"url":null,"abstract":"<div><p>Plant volatile organic compounds are an abundant resource that can be used to explore natural gaseous fungicides. Recently, we found that (<i>E</i>)-2-heptenal, a green leaf volatile, could effectively inhibit the growth of <i>Aspergillus flavus</i>, showing promise for application as a biofumigant to prevent grain spoilage by <i>A. flavus</i>. In this study, the inhibitory effects of (<i>E</i>)-2-heptenal on <i>A. flavus</i> spore germination and mechanisms underlying these effects were investigated through morphological, biochemical, and transcriptomic analyses. The minimum inhibitory concentration and minimum fungicidal concentration of (<i>E</i>)-2-heptenal for spore germination of <i>A. flavus</i> were 4.0 and 6.0 µL/mL, respectively. (<i>E</i>)-2-heptenal treatment resulted in irregularly deformed, collapsed, and ruptured surface morphology of <i>A. flavus</i> spores, as well as destroyed cell wall integrity and reduced ergosterol content in <i>A. flavus</i> spores. Transcriptomic analysis revealed 4,312 differentially expressed genes in <i>A. flavus</i> spores exposed to (<i>E</i>)-2-heptenal, including 1,913 upregulated and 2,399 downregulated genes; these genes were mainly involved in ribosome biogenesis, cell cycle, linoleic acid metabolism, MAPK signaling, nucleoplasmic transport, meiosis, lipoic acid metabolism, DNA replication, and pyruvate metabolism pathways. (<i>E</i>)-2-heptenal can induce reactive oxygen species accumulation and mitochondrial dysfunction in <i>A. flavus</i> spores in a dose-dependent manner. Besides, DNA damage and autophagy was observed in (<i>E</i>)-2-heptenal-treated <i>A. flavus</i> spores with 4′,6-diamidino-2-phenylindole and monodansylcadaverine fluorescence staining. The findings of the present study provide insights into the underlying inhibitory mechanisms of (<i>E</i>)-2-heptenal on <i>A. flavus</i> spore germination.</p></div>","PeriodicalId":564,"journal":{"name":"Food Biophysics","volume":"19 4","pages":"923 - 937"},"PeriodicalIF":2.8000,"publicationDate":"2024-07-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Food Biophysics","FirstCategoryId":"97","ListUrlMain":"https://link.springer.com/article/10.1007/s11483-024-09868-0","RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"FOOD SCIENCE & TECHNOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Plant volatile organic compounds are an abundant resource that can be used to explore natural gaseous fungicides. Recently, we found that (E)-2-heptenal, a green leaf volatile, could effectively inhibit the growth of Aspergillus flavus, showing promise for application as a biofumigant to prevent grain spoilage by A. flavus. In this study, the inhibitory effects of (E)-2-heptenal on A. flavus spore germination and mechanisms underlying these effects were investigated through morphological, biochemical, and transcriptomic analyses. The minimum inhibitory concentration and minimum fungicidal concentration of (E)-2-heptenal for spore germination of A. flavus were 4.0 and 6.0 µL/mL, respectively. (E)-2-heptenal treatment resulted in irregularly deformed, collapsed, and ruptured surface morphology of A. flavus spores, as well as destroyed cell wall integrity and reduced ergosterol content in A. flavus spores. Transcriptomic analysis revealed 4,312 differentially expressed genes in A. flavus spores exposed to (E)-2-heptenal, including 1,913 upregulated and 2,399 downregulated genes; these genes were mainly involved in ribosome biogenesis, cell cycle, linoleic acid metabolism, MAPK signaling, nucleoplasmic transport, meiosis, lipoic acid metabolism, DNA replication, and pyruvate metabolism pathways. (E)-2-heptenal can induce reactive oxygen species accumulation and mitochondrial dysfunction in A. flavus spores in a dose-dependent manner. Besides, DNA damage and autophagy was observed in (E)-2-heptenal-treated A. flavus spores with 4′,6-diamidino-2-phenylindole and monodansylcadaverine fluorescence staining. The findings of the present study provide insights into the underlying inhibitory mechanisms of (E)-2-heptenal on A. flavus spore germination.
期刊介绍:
Biophysical studies of foods and agricultural products involve research at the interface of chemistry, biology, and engineering, as well as the new interdisciplinary areas of materials science and nanotechnology. Such studies include but are certainly not limited to research in the following areas: the structure of food molecules, biopolymers, and biomaterials on the molecular, microscopic, and mesoscopic scales; the molecular basis of structure generation and maintenance in specific foods, feeds, food processing operations, and agricultural products; the mechanisms of microbial growth, death and antimicrobial action; structure/function relationships in food and agricultural biopolymers; novel biophysical techniques (spectroscopic, microscopic, thermal, rheological, etc.) for structural and dynamical characterization of food and agricultural materials and products; the properties of amorphous biomaterials and their influence on chemical reaction rate, microbial growth, or sensory properties; and molecular mechanisms of taste and smell.
A hallmark of such research is a dependence on various methods of instrumental analysis that provide information on the molecular level, on various physical and chemical theories used to understand the interrelations among biological molecules, and an attempt to relate macroscopic chemical and physical properties and biological functions to the molecular structure and microscopic organization of the biological material.