Transcriptional signatures underlying divergent lifestyles of endophytic and pathogenic fungi in early colonisation of wheat roots

Wheat take-all is a root disease which devastates crop yields, caused by the ascomycete fungus Gaeumannomyces tritici . The closely related root endophyte, Gaeumannomyces hyphopodioides , has been found to induce local host defence responses which confer protection against take-all and reduce disease severity. Chancellor et al. (2024) investigated the host transcriptional response to early colonisation by each of these two fungi. Using this RNA-seq dataset in conjunction with newly available Gaeumannomyces reference genomes, we have completed the picture by characterising the fungal transcriptional activity underpinning these different lifestyles. Even at early time points, their transcriptional profiles differ: G. hyphopodioides shows signs of transcriptional reprogramming between 4 and 5 days post inoculation (dpi), mirroring the wheat response. However, G. tritici expression varied very little between these two time points despite progressing into the vasculature, instead exhibiting a stealthy expression profile dominated by gene downregulation at earlier time points. Moreover, GO term enrichment in this study identified a stress response unique to G. hyphopodioides , which may explain the formation of its subepidermal vesicles (SEVs), putative resting structures that represent a key difference between the pathogen and non-pathogen, alongside upregulation of many putative effectors and CAZymes. The enrichment of a key lignin-degrading CAZyme may contribute to the lack of stress-response identified in G. tritici , allowing fungal hyphae to overcome localised host lignification. These findings highlight the transcriptional basis of colonisation differences and are a step towards understanding how closely related fungi with different lifestyles modulate their interactions within a common host and tissue.

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Journal
Fungal Biology
Published
2026-10-27
DOI
https://doi.org/10.1016/j.funbio.2026.101887
Primary Topic
Plant Pathogens and Fungal Diseases
Type
article
Field-Weighted Citation Impact
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article

Transcriptional signatures underlying divergent lifestyles of endophytic and pathogenic fungi in early colonisation of wheat roots

Rowena Hill, Rachel Rusholme‐Pilcher, Tania Chancellor, Kim E. Hammond-Kosack et al.
3 links
Fungal Biology
Plant Pathogens and Fungal Diseases
article

Transcriptional signatures underlying divergent lifestyles of endophytic and pathogenic fungi in early colonisation of wheat roots

Rowena Hill, Rachel Rusholme‐Pilcher, Tania Chancellor, Kim E. Hammond-Kosack, Mark McMullan, Neil Hall, Stella Moren-Rosado
article en

Abstract

Wheat take-all is a root disease which devastates crop yields, caused by the ascomycete fungus Gaeumannomyces tritici . The closely related root endophyte, Gaeumannomyces hyphopodioides , has been found to induce local host defence responses which confer protection against take-all and reduce disease severity. Chancellor et al. (2024) investigated the host transcriptional response to early colonisation by each of these two fungi. Using this RNA-seq dataset in conjunction with newly available Gaeumannomyces reference genomes, we have completed the picture by characterising the fungal transcriptional activity underpinning these different lifestyles. Even at early time points, their transcriptional profiles differ: G. hyphopodioides shows signs of transcriptional reprogramming between 4 and 5 days post inoculation (dpi), mirroring the wheat response. However, G. tritici expression varied very little between these two time points despite progressing into the vasculature, instead exhibiting a stealthy expression profile dominated by gene downregulation at earlier time points. Moreover, GO term enrichment in this study identified a stress response unique to G. hyphopodioides , which may explain the formation of its subepidermal vesicles (SEVs), putative resting structures that represent a key difference between the pathogen and non-pathogen, alongside upregulation of many putative effectors and CAZymes. The enrichment of a key lignin-degrading CAZyme may contribute to the lack of stress-response identified in G. tritici , allowing fungal hyphae to overcome localised host lignification. These findings highlight the transcriptional basis of colonisation differences and are a step towards understanding how closely related fungi with different lifestyles modulate their interactions within a common host and tissue.

Fungal BiologyVol. 130(8)
University of East Anglia (GB), Norwich Research Park (GB), Rothamsted Research (GB), Royal Botanic Gardens, Kew (GB), Earlham Institute (GB)
Biotechnology and Biological Sciences Research Council
Openalex Percentile: Top 16%
Plant Pathogens and Fungal Diseases
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