Patulin inhibition of specific apple microbiome members uncovers Hanseniaspora uvarum as a potential biocontrol agent.

IF 2.6 2区 农林科学 Q2 PLANT SCIENCES Phytopathology Pub Date : 2024-10-07 DOI:10.1094/PHYTO-06-24-0189-R
Justin L Eagan, Evan R Digman, Martijn den Boon, Roberto Regalado, Mira S A Rawa, Christina M Hull, Nancy P Keller
{"title":"Patulin inhibition of specific apple microbiome members uncovers <i>Hanseniaspora uvarum</i> as a potential biocontrol agent.","authors":"Justin L Eagan, Evan R Digman, Martijn den Boon, Roberto Regalado, Mira S A Rawa, Christina M Hull, Nancy P Keller","doi":"10.1094/PHYTO-06-24-0189-R","DOIUrl":null,"url":null,"abstract":"<p><p><i>Penicillium expansum</i> is a major postharvest pathogen of apples, causing loss in fruits through tissue damage, as well as in apple products due to contamination with the mycotoxin patulin. During infections, patulin is a cultivar-dependent virulence factor that facilitates apple lesion development. Patulin also has characterized antimicrobial activity and is important for inhibiting other competitive phytopathogens, but the role of this inhibitory activity has not been investigated in the context of the apple microbiome. In our current study, we isolated 68 apple microbiota and characterized their susceptibility to <i>P. expansum</i> extracts. We found Gram-negative bacteria and Basidiomycete yeast to demonstrate largely patulin-specific growth inhibition compared to Gram-positive and Ascomycete isolates. From co-cultures, we identified a <i>Hanseniaspora</i> and <i>Gluconobacter</i> pairing that reduced <i>P. expansum</i> biomass and found that <i>Hanseniaspora uvarum</i> alone is sufficient to reduce apple disease progression in vivo. We investigated possible mechanisms of <i>H. uvarum</i> biocontrol activity and found modest inhibition on apple puree plates, as well as a trend toward lower patulin levels at the wound site. Active biocontrol activity required live yeast, which also were effective in controlling <i>Botrytis cinerea</i> apple infections. Lastly, we explored the breadth of <i>H. uvarum</i> biocontrol activity with over 30 <i>H. uvarum</i> isolates and found consistent inhibition of <i>P. expansum</i> apple disease.</p>","PeriodicalId":20410,"journal":{"name":"Phytopathology","volume":" ","pages":""},"PeriodicalIF":2.6000,"publicationDate":"2024-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Phytopathology","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1094/PHYTO-06-24-0189-R","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Penicillium expansum is a major postharvest pathogen of apples, causing loss in fruits through tissue damage, as well as in apple products due to contamination with the mycotoxin patulin. During infections, patulin is a cultivar-dependent virulence factor that facilitates apple lesion development. Patulin also has characterized antimicrobial activity and is important for inhibiting other competitive phytopathogens, but the role of this inhibitory activity has not been investigated in the context of the apple microbiome. In our current study, we isolated 68 apple microbiota and characterized their susceptibility to P. expansum extracts. We found Gram-negative bacteria and Basidiomycete yeast to demonstrate largely patulin-specific growth inhibition compared to Gram-positive and Ascomycete isolates. From co-cultures, we identified a Hanseniaspora and Gluconobacter pairing that reduced P. expansum biomass and found that Hanseniaspora uvarum alone is sufficient to reduce apple disease progression in vivo. We investigated possible mechanisms of H. uvarum biocontrol activity and found modest inhibition on apple puree plates, as well as a trend toward lower patulin levels at the wound site. Active biocontrol activity required live yeast, which also were effective in controlling Botrytis cinerea apple infections. Lastly, we explored the breadth of H. uvarum biocontrol activity with over 30 H. uvarum isolates and found consistent inhibition of P. expansum apple disease.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
抑制特定苹果微生物群成员的棒曲霉素发现 Hanseniaspora uvarum 是一种潜在的生物控制剂。
扩张青霉是苹果采后的一种主要病原菌,会因组织损伤造成果实损失,也会因霉菌毒素棒曲霉素污染苹果产品而造成损失。在感染过程中,棒曲霉素是一种取决于栽培品种的毒力因子,可促进苹果病害的发展。棒曲霉素还具有抗菌活性,对抑制其他竞争性植物病原菌非常重要,但这种抑制活性在苹果微生物组中的作用尚未得到研究。在目前的研究中,我们分离了 68 个苹果微生物群,并描述了它们对扩张果实萃取物的敏感性。我们发现,与革兰氏阳性菌和子囊菌分离物相比,革兰氏阴性菌和担子菌酵母在很大程度上表现出抑制棒曲霉素特异性生长的作用。从共培养物中,我们发现了一种能减少扩张菌生物量的汉森氏菌和葡萄糖酵母菌配对,并发现仅汉森氏菌就足以减少苹果病害在体内的发展。我们研究了 H. uvarum 生物防治活性的可能机制,发现在苹果泥平板上有适度的抑制作用,而且伤口部位的棒曲霉素水平有降低的趋势。活跃的生物控制活性需要活酵母,而活酵母也能有效控制苹果灰霉病感染。最后,我们利用 30 多种 H. uvarum 分离物探索了 H. uvarum 生物防治活性的广度,发现它们对扩张果实瘤苹果病害具有一致的抑制作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Phytopathology
Phytopathology 生物-植物科学
CiteScore
5.90
自引率
9.40%
发文量
505
审稿时长
4-8 weeks
期刊介绍: Phytopathology publishes articles on fundamental research that advances understanding of the nature of plant diseases, the agents that cause them, their spread, the losses they cause, and measures that can be used to control them. Phytopathology considers manuscripts covering all aspects of plant diseases including bacteriology, host-parasite biochemistry and cell biology, biological control, disease control and pest management, description of new pathogen species description of new pathogen species, ecology and population biology, epidemiology, disease etiology, host genetics and resistance, mycology, nematology, plant stress and abiotic disorders, postharvest pathology and mycotoxins, and virology. Papers dealing mainly with taxonomy, such as descriptions of new plant pathogen taxa are acceptable if they include plant disease research results such as pathogenicity, host range, etc. Taxonomic papers that focus on classification, identification, and nomenclature below the subspecies level may also be submitted to Phytopathology.
期刊最新文献
Validation of PCR Diagnostic Assays for Detection and Identification of All Ralstonia solanacearum Sequevars Causing Moko Disease in Banana. Building Accelerated Plant Breeding Pipelines: Screening to Evaluate Lima Bean Resistance to Root-Knot Nematode in Diverse Inbred Lines and Segregating Breeding Populations. First Reported Sexual Recombination Between Pyrenophora teres Isolates from Barley and Barley Grass. Mapping Seedling and Adult Plant Leaf Rust Resistance Genes in the Durum Wheat Cultivar Strongfield and Other Triticum turgidum Lines. An Engineered Citrus Tristeza Virus (T36CA)-Based Vector Induces Gene-Specific RNA Silencing and Is Graft Transmissible to Commercial Citrus Varieties.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1