Contrasting transcriptional responses and genetic determinants underlie Zymoseptoria tritici adaptation mechanisms to simulated host-associated environments

Abstract Background Successful colonization of the wheat apoplast requires that Zymoseptoria tritici tolerate host-derived stresses, but the mechanisms underlying this adaptation remain poorly understood. Here, we combined phenotypic assays, transcriptomics, and genome-wide association analyses to characterize fungal responses to acidic pH, salicylic acid, gibberellic acid, and oxidative stress. Results Exposure to salicylic acid inhibited in vitro growth across a global collection of 411 Z. tritici strains, whereas acidic pH promoted growth, illustrating contrasting effects of simulated host-associated environments on pathogen growth. At the transcriptional level, acidic pH and oxidative stress induced the strongest and most similar responses, while salicylic acid elicited a more distinct transcriptional program and gibberellic acid caused only limited transcriptional changes. Although the sets of differentially expressed genes were largely condition specific, overlapping enrichment of transport- and redox-related functions across conditions indicated shared transcriptional responses. K -mer based genome-wide association mapping identified five candidate loci associated with growth under acidic pH, gibberellic acid, and salicylic acid, including four loci specific to individual growth conditions. These loci colocalized with genes implicated in cell wall remodeling, nitrogen metabolite regulation, proteostasis, and ubiquitin-related processes. Conclusion This study highlights the capacity of Z. tritici to tailor its responses to simulated host-associated environments through a combination of shared and environment-specific mechanisms. We provide new insights into the genetic and molecular basis of fungal resilience, with implications for understanding pathogen-host interactions.

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Publication Details

Journal
BMC Genomics
Published
2026-09-22
DOI
https://doi.org/10.1186/s12864-026-13300-x
Primary Topic
Fungal and yeast genetics research
Type
article
Field-Weighted Citation Impact
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article

Contrasting transcriptional responses and genetic determinants underlie Zymoseptoria tritici adaptation mechanisms to simulated host-associated environments

Alice Feurtey, Cécile Lorrain, Bruce A. McDonald, Silvia Miñana-Posada
BMC Genomics
Fungal and yeast genetics research
article

Contrasting transcriptional responses and genetic determinants underlie Zymoseptoria tritici adaptation mechanisms to simulated host-associated environments

Alice Feurtey, Cécile Lorrain, Bruce A. McDonald, Silvia Miñana-Posada
article en

Abstract

Abstract Background Successful colonization of the wheat apoplast requires that Zymoseptoria tritici tolerate host-derived stresses, but the mechanisms underlying this adaptation remain poorly understood. Here, we combined phenotypic assays, transcriptomics, and genome-wide association analyses to characterize fungal responses to acidic pH, salicylic acid, gibberellic acid, and oxidative stress. Results Exposure to salicylic acid inhibited in vitro growth across a global collection of 411 Z. tritici strains, whereas acidic pH promoted growth, illustrating contrasting effects of simulated host-associated environments on pathogen growth. At the transcriptional level, acidic pH and oxidative stress induced the strongest and most similar responses, while salicylic acid elicited a more distinct transcriptional program and gibberellic acid caused only limited transcriptional changes. Although the sets of differentially expressed genes were largely condition specific, overlapping enrichment of transport- and redox-related functions across conditions indicated shared transcriptional responses. K -mer based genome-wide association mapping identified five candidate loci associated with growth under acidic pH, gibberellic acid, and salicylic acid, including four loci specific to individual growth conditions. These loci colocalized with genes implicated in cell wall remodeling, nitrogen metabolite regulation, proteostasis, and ubiquitin-related processes. Conclusion This study highlights the capacity of Z. tritici to tailor its responses to simulated host-associated environments through a combination of shared and environment-specific mechanisms. We provide new insights into the genetic and molecular basis of fungal resilience, with implications for understanding pathogen-host interactions.

BMC Genomics
Christian-Albrechts-Universität zu Kiel (DE), ETH Zurich (CH)
Life in Land
Openalex Percentile: Top 18%
Fungal and yeast genetics research
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