Horizontal transfers between fungal Fusarium species contributed to successive outbreaks of coffee wilt disease.

IF 9.8 1区 生物学 Q1 Agricultural and Biological Sciences
PLoS Biology Pub Date : 2024-12-05 eCollection Date: 2024-12-01 DOI:10.1371/journal.pbio.3002480
Lily D Peck, Theo Llewellyn, Bastien Bennetot, Samuel O'Donnell, Reuben W Nowell, Matthew J Ryan, Julie Flood, Ricardo C Rodríguez de la Vega, Jeanne Ropars, Tatiana Giraud, Pietro D Spanu, Timothy G Barraclough
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引用次数: 0

Abstract

Outbreaks of fungal diseases have devastated plants and animals throughout history. Over the past century, the repeated emergence of coffee wilt disease caused by the fungal pathogen Fusarium xylarioides severely impacted coffee production across sub-Saharan Africa. To improve the disease management of such pathogens, it is crucial to understand their genetic structure and evolutionary potential. We compared the genomes of 13 historic strains spanning 6 decades and multiple disease outbreaks to investigate population structure and host specialisation. We found that F. xylarioides comprised at least 4 distinct lineages: 1 host-specific to Coffea arabica, 1 to C. canephora var. robusta, and 2 historic lineages isolated from various Coffea species. The presence/absence of large genomic regions across populations, the higher genetic similarities of these regions between species than expected based on genome-wide divergence and their locations in different loci in genomes across populations showed that horizontal transfers of effector genes from members of the F. oxysporum species complex contributed to host specificity. Multiple transfers into F. xylarioides populations matched different parts of the F. oxysporum mobile pathogenicity chromosome and were enriched in effector genes and transposons. Effector genes in this region and other carbohydrate-active enzymes important in the breakdown of plant cell walls were shown by transcriptomics to be highly expressed during infection of C. arabica by the fungal arabica strains. Widespread sharing of specific transposons between F. xylarioides and F. oxysporum, and the correspondence of a putative horizontally transferred regions to a Starship (large mobile element involved in horizontal gene transfers in fungi), reinforce the inference of horizontal transfers and suggest that mobile elements were involved. Our results support the hypothesis that horizontal gene transfers contributed to the repeated emergence of coffee wilt disease.

镰刀菌种类之间的水平转移导致了咖啡枯萎病的连续爆发。
历史上,真菌疾病的爆发摧毁了植物和动物。在过去的一个世纪里,由真菌病原菌木镰刀菌引起的咖啡枯萎病的反复出现严重影响了撒哈拉以南非洲地区的咖啡生产。为了改善这些病原体的疾病管理,了解它们的遗传结构和进化潜力是至关重要的。我们比较了跨越60年和多次疾病暴发的13个历史菌株的基因组,以调查种群结构和宿主专业化。结果表明,木木孢子虫至少包含4个不同的谱系:1个是阿拉比卡咖啡特有的寄主谱系,1个是canephora var. robusta特有的寄主谱系,以及2个从不同咖啡物种中分离出来的历史谱系。大基因组区域在种群间的存在/缺失,这些区域在物种间的遗传相似性高于基于全基因组差异的预期,以及它们在种群间基因组中不同位点的位置,表明来自尖孢镰刀菌物种复合物成员的效应基因的水平转移有助于宿主特异性。在木孢子菌群体中的多次转移与木孢子菌移动致病性染色体的不同部分相匹配,并富集了效应基因和转座子。转录组学表明,在小比卡菌侵染小比卡菌时,该区域的效应基因和其他在植物细胞壁破坏中重要的碳水化合物活性酶被高度表达。在xylarioides和f.s oxysporum之间广泛共享特定转座子,以及假定的水平转移区域与Starship的对应(真菌中参与水平基因转移的大型移动元件),加强了水平转移的推断,并表明移动元件参与了水平转移。我们的研究结果支持了水平基因转移导致咖啡枯萎病反复出现的假设。
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来源期刊
PLoS Biology
PLoS Biology BIOCHEMISTRY & MOLECULAR BIOLOGY-BIOLOGY
CiteScore
15.40
自引率
2.00%
发文量
359
审稿时长
3-8 weeks
期刊介绍: PLOS Biology is the flagship journal of the Public Library of Science (PLOS) and focuses on publishing groundbreaking and relevant research in all areas of biological science. The journal features works at various scales, ranging from molecules to ecosystems, and also encourages interdisciplinary studies. PLOS Biology publishes articles that demonstrate exceptional significance, originality, and relevance, with a high standard of scientific rigor in methodology, reporting, and conclusions. The journal aims to advance science and serve the research community by transforming research communication to align with the research process. It offers evolving article types and policies that empower authors to share the complete story behind their scientific findings with a diverse global audience of researchers, educators, policymakers, patient advocacy groups, and the general public. PLOS Biology, along with other PLOS journals, is widely indexed by major services such as Crossref, Dimensions, DOAJ, Google Scholar, PubMed, PubMed Central, Scopus, and Web of Science. Additionally, PLOS Biology is indexed by various other services including AGRICOLA, Biological Abstracts, BIOSYS Previews, CABI CAB Abstracts, CABI Global Health, CAPES, CAS, CNKI, Embase, Journal Guide, MEDLINE, and Zoological Record, ensuring that the research content is easily accessible and discoverable by a wide range of audiences.
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