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

2024/12/05 by Lily D. Peck, Theo Llewellyn, Bastien Bennetot +9 · 1 voice · 23 citations
Agricultural and Biological Sciences · Biochemistry, Genetics and Molecular Biology · #Biology #Botany #Coffea arabica #Effector #Fusarium oxysporum #Gene #Genetics #Genome #Genome evolution #Horizontal gene transfer #Host (biology) #Mobile genetic elements #Outbreak #Plant Pathogens and Fungal Diseases #Plant and Fungal Interactions Research #Plant-Microbe Interactions and Immunity #Population #Virology

paper · doi:10.1371/journal.pbio.3002480

published in PLoS Biology 22(12), e3002480 (Public Library of Science)

openalex publication_date 2024/12/05 · openalex created_date 2025/10/10 · openalex updated_date 2026/07/31

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.

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