# Transcriptomic and metabolomic analyses unravel the different pathogenic mechanisms of Ustilaginoidea virens in indica and japonica rice

**Authors:** Rongtao Fu, Yu Chen, Cheng Chen, Jian Wang, Liyu Zhao, Daihua Lu

PMC · DOI: 10.3389/fmicb.2025.1680221 · Frontiers in Microbiology · 2025-10-17

## TL;DR

This study uses transcriptomic and metabolomic analyses to uncover how the rice false smut fungus affects indica and japonica rice varieties differently.

## Contribution

The study reveals distinct pathogenic mechanisms of Ustilaginoidea virens in different rice varieties through combined transcriptomic and metabolomic analyses.

## Key findings

- Susceptible indica rice variety 'GuiChao2' had more diseased grains than japonica variety 'Zhejing99' under same inoculation conditions.
- Differential gene expression and metabolite accumulation patterns were observed in U. virens after infecting indica and japonica rice.
- Pathways like MAPK signaling, lysine biosynthesis, and amino acid metabolism showed varied responses in different rice varieties.

## Abstract

Rice false smut (RFS) caused by the fungal pathogen Ustilaginoidea virens (Cook) produces high yield losses in rice. Rice varieties differ in their resistance to RFS. However, the pathogenic mechanism of the fungus U. virens in different varieties remains unclear. In our study, transcriptome and metabolome analyses were performed on U. virens after 5 and 7 days after infection in indica and japonica rice to reveal different pathogenic mechanisms. Interestingly, we discovered that the average number of diseased grains of the susceptible variety “GuiChao2” (indica rice) was higher than that of the susceptible variety “Zhejing99” (japonica rice) under the same inoculation conditions. In all, 6,073, 5,795, 4,251, and 5,978 differentially expressed genes (DEGs) were shared among the four infected rice compared with the control group. In this study, there were differences in the types and quantities of transcription factors in U. virens after infection of indica and japonica rice. A Kyoto Encyclopedia of Genes and Genomes analysis showed that the DEGs involved in the mitogen-activated protein kinase signaling pathway, autophagy–yeast, lysine biosynthesis, phenylalanine metabolism, and tryptophan metabolism responded to infection, and the expression patterns of key regulatory genes, including STE, ATG, CYP, and LYS differed after infection indica and japonica rice. The results of a metabolome analysis indicated that the differentially accumulated metabolites (DAMs) mainly were significantly enrichment in pathways included amino acids, lipids, and nucleosides, and the accumulation patterns between infected indica and japonica rice differed. Furthermore, the combined transcriptome and metabolome analysis revealed that different DAMs regulated by different DEGs produced variations in the pathogenicity of U. virens infection in indica and japonica rice. Hence, this study provides insight into the molecular mechanisms related to U. virens infection in different rice varieties.

## Linked entities

- **Genes:** SULT1E1 (sulfotransferase family 1E member 1) [NCBI Gene 6783], Atg1 (Autophagy-related 1) [NCBI Gene 39454], PPIG (peptidylprolyl isomerase G) [NCBI Gene 9360], lys (endolysin) [NCBI Gene 921041]
- **Species:** Ustilaginoidea virens (taxon 1159556)

## Full-text entities

- **Chemicals:** lipids (MESH:D008055), amino acids (MESH:D000596), lysine (MESH:D008239), tryptophan (MESH:D014364), phenylalanine (MESH:D010649), nucleosides (MESH:D009705)
- **Species:** Oryza sativa Japonica Group (Japanese rice, no rank) [taxon 39947], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Ustilaginoidea virens (rice false smut, species) [taxon 1159556], Oryza sativa Indica Group (Indian rice, no rank) [taxon 39946], U. virens [taxon 124427], Oryza sativa (Asian cultivated rice, species) [taxon 4530]

## Full text

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## Figures

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## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12576890/full.md

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Source: https://tomesphere.com/paper/PMC12576890