Maryke Carstens , Clara Pliego , Annabel Norval , Noëlani van den Berg
{"title":"Dematophora necatrix: From taxonomy to molecular advances","authors":"Maryke Carstens , Clara Pliego , Annabel Norval , Noëlani van den Berg","doi":"10.1016/j.fbr.2026.100471","DOIUrl":null,"url":null,"abstract":"<div><div><em>Dematophora necatrix</em> Hartig is a destructive soil-borne fungus responsible for White Root Rot (WRR), affecting more than 350 plant species across 51 countries, including many economically important crops. The pathogen's persistence in soil and broad host range makes it especially challenging to control. Over the past decade, molecular studies have significantly advanced our understanding of the pathogen's biology and its interactions with host plants. These developments underscore the need for a comprehensive review to consolidate recent scientific progress. First, we outline the taxonomy, biology, disease symptoms, hosts and global distribution, and current management strategies of <em>D. necatrix</em>. We then focus on recent molecular advances, highlighting how genomics, transcriptomics, proteomics and metabolomics studies have improved our understanding of the pathogen's virulence and pathogenicity. A high-quality, chromosome-level genome assembly has enabled more precise annotation and gene prediction. Transcriptomic analyses have identified candidate pathogenicity-related genes and putative effectors, while secretome proteomic studies suggest the production of antimicrobial proteins which may facilitate infection by suppressing microbial competitors. Secondary metabolites, such as cytochalasin E, have been implicated in virulence, although their precise roles in pathogenicity remain unresolved. Improved transformation protocols now permit targeted gene manipulation, creating new opportunities for functional studies. Lastly, this review highlights key knowledge gaps and calls for integrated multi-omics approaches to better understand <em>D. necatrix</em> pathogenicity and virulence, long-term survival, and environmental adaptation. Such insights are critical for the development of durable, targeted strategies to manage WRR.</div></div>","PeriodicalId":12563,"journal":{"name":"Fungal Biology Reviews","volume":"55 ","pages":"Article 100471"},"PeriodicalIF":4.6000,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fungal Biology Reviews","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1749461326000011","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/19 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"MYCOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Dematophora necatrix Hartig is a destructive soil-borne fungus responsible for White Root Rot (WRR), affecting more than 350 plant species across 51 countries, including many economically important crops. The pathogen's persistence in soil and broad host range makes it especially challenging to control. Over the past decade, molecular studies have significantly advanced our understanding of the pathogen's biology and its interactions with host plants. These developments underscore the need for a comprehensive review to consolidate recent scientific progress. First, we outline the taxonomy, biology, disease symptoms, hosts and global distribution, and current management strategies of D. necatrix. We then focus on recent molecular advances, highlighting how genomics, transcriptomics, proteomics and metabolomics studies have improved our understanding of the pathogen's virulence and pathogenicity. A high-quality, chromosome-level genome assembly has enabled more precise annotation and gene prediction. Transcriptomic analyses have identified candidate pathogenicity-related genes and putative effectors, while secretome proteomic studies suggest the production of antimicrobial proteins which may facilitate infection by suppressing microbial competitors. Secondary metabolites, such as cytochalasin E, have been implicated in virulence, although their precise roles in pathogenicity remain unresolved. Improved transformation protocols now permit targeted gene manipulation, creating new opportunities for functional studies. Lastly, this review highlights key knowledge gaps and calls for integrated multi-omics approaches to better understand D. necatrix pathogenicity and virulence, long-term survival, and environmental adaptation. Such insights are critical for the development of durable, targeted strategies to manage WRR.
期刊介绍:
Fungal Biology Reviews is an international reviews journal, owned by the British Mycological Society. Its objective is to provide a forum for high quality review articles within fungal biology. It covers all fields of fungal biology, whether fundamental or applied, including fungal diversity, ecology, evolution, physiology and ecophysiology, biochemistry, genetics and molecular biology, cell biology, interactions (symbiosis, pathogenesis etc), environmental aspects, biotechnology and taxonomy. It considers aspects of all organisms historically or recently recognized as fungi, including lichen-fungi, microsporidia, oomycetes, slime moulds, stramenopiles, and yeasts.