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{"title":"<i>Lasiodiplodia theobromae</i> as a Model Latent Pathogen: Molecular Mechanisms, Global Impact, and Sustainable Management.","authors":"Synan F AbuQamar, Arshiya Akbar, Gouthaman P Purayil, Khaled A El-Tarabily","doi":"10.1094/MPMI-07-26-0067-IRW","DOIUrl":null,"url":null,"abstract":"<p><p><i>Lasiodiplodia theobromae</i> (Botryosphaeriaceae) is a cosmopolitan ascomycete that endophytically colonizes over 500 plant species and switches to necrotrophy under host stress. In mango (<i>Mangifera indica</i>), it causes stem-end rot, dieback, gummosis, and collar rot, driving substantial pre- and postharvest losses worldwide. This review integrates five thematic areas: (i) multilocus phylogenetics (<i>ITS</i>, <i>tef1-</i>α, <i>tub2</i>, and <i>rpb2</i>) resolving cryptic species within the <i>L. theobromae</i> species complex; (ii) disease epidemiology centered on latent colonization of inflorescences and stress-triggered activation; (iii) molecular pathogenicity mechanisms, including secreted effectors, cell wall-degrading enzymes, fungal phytohormones, and regulatory small RNAs; (iv) multi-omics advances revealing expanded CAZyme and secondary metabolite biosynthetic gene clusters, plus emerging multi-class fungicide resistance (MBC, QoI, and DMI) driven by β<i>-tubulin</i> mutations, alternative oxidase upregulation, and <i>CYP51</i> overexpression; and (v) sustainable biological control using <i>Streptomyces</i>, <i>Bacillus</i>, and <i>Trichoderma</i> strains, alongside host priming with hexanal or methyl jasmonate. We propose a testable model wherein environmental triggers (temperature and drought) and host hormone balance (ethylene and jasmonic acid-salicylic acid crosstalk) converge temperature-regulated virulence gene expression to govern the endophyte-to-necrotroph transition. Critical gaps include the limited genomic resources for mango-derived isolates, infection-stage dual RNA-seq, population genetics, and climate-informed epidemiological models. Future directions encompass CRISPR-enabled susceptibility gene editing, RNAi biocontrol, and integrated pest management tailored to this latent pathogen. [Formula: see text] Copyright © 2026 The Author(s). This is an open access article distributed under the CC BY-NC-ND 4.0 International license.</p>","PeriodicalId":19009,"journal":{"name":"Molecular Plant-microbe Interactions","volume":" ","pages":"MPMI07260067IRW"},"PeriodicalIF":3.9000,"publicationDate":"2026-09-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Plant-microbe Interactions","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1094/MPMI-07-26-0067-IRW","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
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Abstract
Lasiodiplodia theobromae (Botryosphaeriaceae) is a cosmopolitan ascomycete that endophytically colonizes over 500 plant species and switches to necrotrophy under host stress. In mango (Mangifera indica ), it causes stem-end rot, dieback, gummosis, and collar rot, driving substantial pre- and postharvest losses worldwide. This review integrates five thematic areas: (i) multilocus phylogenetics (ITS , tef1- α, tub2 , and rpb2 ) resolving cryptic species within the L. theobromae species complex; (ii) disease epidemiology centered on latent colonization of inflorescences and stress-triggered activation; (iii) molecular pathogenicity mechanisms, including secreted effectors, cell wall-degrading enzymes, fungal phytohormones, and regulatory small RNAs; (iv) multi-omics advances revealing expanded CAZyme and secondary metabolite biosynthetic gene clusters, plus emerging multi-class fungicide resistance (MBC, QoI, and DMI) driven by β-tubulin mutations, alternative oxidase upregulation, and CYP51 overexpression; and (v) sustainable biological control using Streptomyces , Bacillus , and Trichoderma strains, alongside host priming with hexanal or methyl jasmonate. We propose a testable model wherein environmental triggers (temperature and drought) and host hormone balance (ethylene and jasmonic acid-salicylic acid crosstalk) converge temperature-regulated virulence gene expression to govern the endophyte-to-necrotroph transition. Critical gaps include the limited genomic resources for mango-derived isolates, infection-stage dual RNA-seq, population genetics, and climate-informed epidemiological models. Future directions encompass CRISPR-enabled susceptibility gene editing, RNAi biocontrol, and integrated pest management tailored to this latent pathogen. [Formula: see text] Copyright © 2026 The Author(s). This is an open access article distributed under the CC BY-NC-ND 4.0 International license.
作为模型潜伏病原体的可可残丝虫:分子机制、全球影响和可持续管理。
牛膝球囊菌(Lasiodiplodia theobromae, Botryosphaeriaceae)是一种世界性的子囊菌,其内生定植超过500种植物,并在寄主胁迫下转向坏死。在芒果(Mangifera indica)中,它会导致茎端腐病、枯死、牙龈病和果圈腐病,在全球范围内造成大量采前和采后损失。本文综述了5个主题领域:(i)多位点系统发育(ITS, tef1-α, tub2和rpb2)分析了苦苣苔物种复合体中的隐种;(ii)以花序的潜在定植和应激触发激活为中心的疾病流行病学;(iii)分子致病性机制,包括分泌效应物、细胞壁降解酶、真菌植物激素和调节性小rna;(iv)多组学进展揭示了扩大的CAZyme和次生代谢物生物合成基因簇,以及由β-微管蛋白突变、选择性氧化酶上调和CYP51过表达驱动的多类杀菌剂抗性(MBC、qi和DMI);(v)利用链霉菌、芽孢杆菌和木霉菌株进行可持续的生物防治,同时用己醛或茉莉酸甲酯引发宿主。我们提出了一个可测试的模型,其中环境触发因素(温度和干旱)和宿主激素平衡(乙烯和茉莉酸-水杨酸串音)收敛温度调节的毒力基因表达,以控制内生菌向坏死细胞的转变。关键的空白包括芒果源分离株的有限基因组资源、感染期双RNA-seq、群体遗传学和气候信息流行病学模型。未来的发展方向包括crispr易感基因编辑、RNAi生物防治以及针对这种潜在病原体的综合害虫管理。[公式:见正文]版权所有©2026作者。这是一篇在CC BY-NC-ND 4.0国际许可下发布的开放获取文章。
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