PdEch1 regulates the conidia production of Penicillium digitatum and oxidative stress tolerance.

IF 2 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Genes & genomics Pub Date : 2026-10-01 Epub Date: 2026-08-12 DOI:10.1007/s13258-026-01787-3
Lu Yang, Yuqing Wang, Zhonghuan Tian, Chao-An Long
{"title":"PdEch1 regulates the conidia production of Penicillium digitatum and oxidative stress tolerance.","authors":"Lu Yang, Yuqing Wang, Zhonghuan Tian, Chao-An Long","doi":"10.1007/s13258-026-01787-3","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Citrus is the most widely cultivated fruit crop with the highest yield worldwide, and postharvest losses caused by Penicillium digitatum account for 90% of the total postharvest losses in citrus. Enoyl-CoA hydratase (ECH) catalyzes the second step of β-oxidation, the primary pathway of fatty acid catabolism. Previous studies have shown that ECH deficiency causes developmental delay, mitochondrial dysfunction, nervous system damage and other symptoms, and these phenotypes have been reported in humans, mice and Drosophila.</p><p><strong>Objective: </strong>This study aimed to characterize the biological function of the PdEch1 gene in P. digitatum.</p><p><strong>Methods: </strong>The PdEch1 gene deletion strain ΔPdEch1 and complemented strain ΔPdEch1-C were constructed via Agrobacterium-mediated genetic transformation. Physiological assays were performed, including mycelial growth rate measurement, conidial yield quantification, conidial germination rate assay, stress agent sensitivity testing, and pathogenicity evaluation. In addition, transcriptome sequencing and quantitative real-time PCR (qRT-PCR) were conducted.</p><p><strong>Results: </strong>Deletion of PdEch1 increased conidial production by 51.4% and altered the expression of conidiation-related genes such as brlA and rodA. Furthermore, the ΔPdEch1 strain exhibited significantly enhanced resistance to H<sub>2</sub>O<sub>2</sub>. Compared with the wild-type strain N1, mycelial growth, conidial germination, and pathogenicity of P. digitatum were not affected.</p><p><strong>Conclusions: </strong>This study reveals that the PdEch1 gene is closely associated with conidial formation and oxidative stress tolerance in P. digitatum, providing a reference for the development and screening of target sites for novel fungicides.</p>","PeriodicalId":12675,"journal":{"name":"Genes & genomics","volume":" ","pages":"1311-1323"},"PeriodicalIF":2.0000,"publicationDate":"2026-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Genes & genomics","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s13258-026-01787-3","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/8/12 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Citrus is the most widely cultivated fruit crop with the highest yield worldwide, and postharvest losses caused by Penicillium digitatum account for 90% of the total postharvest losses in citrus. Enoyl-CoA hydratase (ECH) catalyzes the second step of β-oxidation, the primary pathway of fatty acid catabolism. Previous studies have shown that ECH deficiency causes developmental delay, mitochondrial dysfunction, nervous system damage and other symptoms, and these phenotypes have been reported in humans, mice and Drosophila.

Objective: This study aimed to characterize the biological function of the PdEch1 gene in P. digitatum.

Methods: The PdEch1 gene deletion strain ΔPdEch1 and complemented strain ΔPdEch1-C were constructed via Agrobacterium-mediated genetic transformation. Physiological assays were performed, including mycelial growth rate measurement, conidial yield quantification, conidial germination rate assay, stress agent sensitivity testing, and pathogenicity evaluation. In addition, transcriptome sequencing and quantitative real-time PCR (qRT-PCR) were conducted.

Results: Deletion of PdEch1 increased conidial production by 51.4% and altered the expression of conidiation-related genes such as brlA and rodA. Furthermore, the ΔPdEch1 strain exhibited significantly enhanced resistance to H2O2. Compared with the wild-type strain N1, mycelial growth, conidial germination, and pathogenicity of P. digitatum were not affected.

Conclusions: This study reveals that the PdEch1 gene is closely associated with conidial formation and oxidative stress tolerance in P. digitatum, providing a reference for the development and screening of target sites for novel fungicides.

PdEch1调控指状青霉分生孢子的产生和氧化应激耐受性。
背景:柑橘是世界上种植最广泛、产量最高的水果作物,指状青霉菌造成的采后损失占柑橘采后损失总量的90%。烯酰辅酶a水合酶(ECH)催化β-氧化的第二步,脂肪酸分解代谢的主要途径。先前的研究表明,ECH缺乏会导致发育迟缓、线粒体功能障碍、神经系统损伤等症状,这些表型在人类、小鼠和果蝇中都有报道。目的:研究指地黄PdEch1基因的生物学功能。方法:通过农杆菌介导的遗传转化,构建PdEch1基因缺失菌株ΔPdEch1和互补菌株ΔPdEch1-C。生理试验包括菌丝生长率测定、分生孢子产量定量、分生孢子发芽率测定、应激剂敏感性试验和致病性评价。此外,还进行了转录组测序和实时定量PCR (qRT-PCR)。结果:PdEch1的缺失使分生孢子产量增加51.4%,并改变了分生孢子相关基因brlA和rodA的表达。此外,ΔPdEch1菌株对H2O2的抗性显著增强。与野生型N1相比,对指革霉菌丝生长、分生孢子萌发和致病性没有影响。结论:本研究揭示了PdEch1基因与指地黄分生孢子形成和氧化应激耐受性密切相关,为新型杀菌剂靶点的开发和筛选提供了参考。
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 求助全文
来源期刊
Genes & genomics
Genes & genomics 生物-生化与分子生物学
CiteScore
3.70
自引率
4.80%
发文量
131
审稿时长
6-12 weeks
期刊介绍: Genes & Genomics is an official journal of the Korean Genetics Society (http://kgenetics.or.kr/). Although it is an official publication of the Genetics Society of Korea, membership of the Society is not required for contributors. It is a peer-reviewed international journal publishing print (ISSN 1976-9571) and online version (E-ISSN 2092-9293). It covers all disciplines of genetics and genomics from prokaryotes to eukaryotes from fundamental heredity to molecular aspects. The articles can be reviews, research articles, and short communications.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书