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Peer-reviewedCC BYBMC Plant Biology

Integrated transcriptome and hormone dynamics uncover biphasic defense responses in sugar beet infected by Cercospora beticola

  1. 1Department of Plant Pathology, Biotechnology, and Microbiology, North Dakota State University
  2. 2Sugarbeet Research Unit, Department of Agriculture- Agricultural Research Service

Abstract

Background Cercospora leaf spot (CLS), caused by the hemibiotrophic fungus Cercospora beticola, is a destructive foliar disease that threatens sugar beet production worldwide. Despite its economic significance, the molecular interaction between sugar beet and C. beticola is poorly understood. Results We report integrated time-resolved transcriptomics and hormone profiling of CLS infection spanning the asymptomatic and symptomatic phases. Our data revealed broad transcriptional changes, with defense and hormone-related processes being most altered. We detected transcriptional signatures consistent with activation of pathogen-associated molecular pattern- and effector-triggered immunity, along with differential expression of genes encoding putative receptor-like kinases and receptor-like proteins as well as nucleotide-binding (NB) leucine‑rich repeat (LRR) receptors (NLRs). Defense activation was evident as early as 3 days post-inoculation (dpi), including upregulation of pathogenesis-related proteins, genes related to systemic acquired resistance, and the hypersensitive response (HR). At 7 dpi, several biological processes, including defense response, showed overall downregulation, suggesting a pathogen-mediated suppression of transcriptional responses. During the symptomatic phase, defense-related genes—particularly those associated with HR and numerous putative NLRs—were induced again, illustrating a bi-phasic regulation pattern. Cis-element enrichment analysis showed significant overrepresentation of defense-related WRKY and AT-hook motif nuclear-localized protein binding motifs within the protomers of genes upregulated from 11 to 25 dpi. Parallel quantification of major phytohormones demonstrated stage-dependent modulation of infection-related hormone groups across the infection cycle. Conclusion Our analysis revealed that a susceptible sugar beet genotype mounts an early and transient defense response against C. beticola, which appears to be pathogen-suppressed but later reactivated during symptom development. By integrating time-resolved transcriptome analysis and hormone profiling, our study links major defense transcriptional programs and phytohormone dynamics, providing a comprehensive view of sugar beet responses to CLS that complements and extends previous genotype-focused work.

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BibTeX
@article{ebinezer2026integrated,
  title = {{Integrated transcriptome and hormone dynamics uncover biphasic defense responses in sugar beet infected by Cercospora beticola}},
  author = {Leonard Barnabas Ebinezer and Mari Natwick and Lorena I. Rangel and Rajdeep Jaswal and Eric Branch and Gary Secor and Melvin D. Bolton and Nathan A. Wyatt},
  journal = {BMC Plant Biology},
  year = {2026},
  month = jul,
  doi = {10.1186/s12870-026-09498-3},
  url = {https://doi.org/10.1186/s12870-026-09498-3},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - Integrated transcriptome and hormone dynamics uncover biphasic defense responses in sugar beet infected by Cercospora beticola
AU  - Leonard Barnabas Ebinezer
AU  - Mari Natwick
AU  - Lorena I. Rangel
AU  - Rajdeep Jaswal
AU  - Eric Branch
AU  - Gary Secor
AU  - Melvin D. Bolton
AU  - Nathan A. Wyatt
PY  - 2026
DA  - 2026/07/01
JO  - BMC Plant Biology
DO  - 10.1186/s12870-026-09498-3
UR  - https://doi.org/10.1186/s12870-026-09498-3
AB  - Background Cercospora leaf spot (CLS), caused by the hemibiotrophic fungus Cercospora beticola, is a destructive foliar disease that threatens sugar beet production worldwide. Despite its economic significance, the molecular interaction between sugar beet and C. beticola is poorly understood. Results We report integrated time-resolved transcriptomics and hormone profiling of CLS infection spanning the asymptomatic and symptomatic phases. Our data revealed broad transcriptional changes, with defense and hormone-related processes being most altered. We detected transcriptional signatures consistent with activation of pathogen-associated molecular pattern- and effector-triggered immunity, along with differential expression of genes encoding putative receptor-like kinases and receptor-like proteins as well as nucleotide-binding (NB) leucine‑rich repeat (LRR) receptors (NLRs). Defense activation was evident as early as 3 days post-inoculation (dpi), including upregulation of pathogenesis-related proteins, genes related to systemic acquired resistance, and the hypersensitive response (HR). At 7 dpi, several biological processes, including defense response, showed overall downregulation, suggesting a pathogen-mediated suppression of transcriptional responses. During the symptomatic phase, defense-related genes—particularly those associated with HR and numerous putative NLRs—were induced again, illustrating a bi-phasic regulation pattern. Cis-element enrichment analysis showed significant overrepresentation of defense-related WRKY and AT-hook motif nuclear-localized protein binding motifs within the protomers of genes upregulated from 11 to 25 dpi. Parallel quantification of major phytohormones demonstrated stage-dependent modulation of infection-related hormone groups across the infection cycle. Conclusion Our analysis revealed that a susceptible sugar beet genotype mounts an early and transient defense response against C. beticola, which appears to be pathogen-suppressed but later reactivated during symptom development. By integrating time-resolved transcriptome analysis and hormone profiling, our study links major defense transcriptional programs and phytohormone dynamics, providing a comprehensive view of sugar beet responses to CLS that complements and extends previous genotype-focused work.
SN  - 1471-2229
ER  -