# GSNOR is essential for nitric oxide homeostasis and involved in aflatoxin biosynthesis and pathogenicity in Aspergillus flavus

**Authors:** Dongyue Chen, Yuan Jiao, Xinping Wang, Fang Tao

PMC · DOI: 10.1128/aem.01408-25 · Applied and Environmental Microbiology · 2025-12-16

## TL;DR

This study shows that GSNOR, an enzyme regulating nitric oxide levels, is vital for the growth, toxin production, and pathogenicity of the fungus Aspergillus flavus.

## Contribution

The study identifies GSNOR's role in NO homeostasis and aflatoxin biosynthesis in Aspergillus flavus, suggesting it as a potential target for aflatoxin prevention.

## Key findings

- GSNOR deletion in Aspergillus flavus leads to elevated NO levels and increased sensitivity to NO stress.
- GSNOR is essential for fungal development, conidiogenesis, and aflatoxin production.
- GSNOR helps maintain ROS balance and protects against oxidative stress in the fungus.

## Abstract

Nitric oxide (NO) is an important biological signaling molecule. S-nitrosoglutathione reductase (GSNOR), a master regulator of NO signaling, regulates various biological processes. However, little is known about the role of GSNOR in Aspergillus flavus. Here, we identified a gene encoding GSNOR in this aflatoxigenic fungus and demonstrated that GSNOR shows activity during the critical life cycle stages, including spore germination, hyphal growth, and conidiogenesis. We found that GSNOR plays a crucial role in NO homeostasis, as GSNOR deletion resulted in significantly elevated NO levels and heightened sensitivity to exogenous NO stress. GSNOR also participated in multiple biological processes in A. flavus; for that, GSNOR deletion impaired conidia germination, reduced growth, decreased conidiogenesis and sclerotial development, attenuated virulence on kernels, and notably decreased aflatoxin production. Furthermore, we demonstrated that GSNOR is important for reactive oxygen species (ROS) balance, as its deletion significantly elevated mycelial ROS levels and made the strain more sensitive to oxidative stress.

Aspergillus flavus is a notorious saprophytic filamentous fungus, with its production of carcinogenic aflatoxins posing serious threats to food safety and human health. Aflatoxin contamination prevention and control have long been a global challenge. In previous studies, we observed that nitric oxide (NO) significantly inhibits the aflatoxin production by A. flavus. This study further investigated the role of the key regulatory enzyme S-nitrosoglutathione reductase (GSNOR) in the NO signaling pathway. Our findings indicate that GSNOR is crucial for maintaining both NO homeostasis and reactive oxygen species (ROS) balance and plays an essential role in fungal development, pathogenicity, and aflatoxin biosynthesis. These results highlight the potential of targeting components in the NO signaling pathway, such as GSNOR, as a novel strategy for the early prevention of aflatoxin contamination in food.

## Linked entities

- **Genes:** ADH5 (alcohol dehydrogenase 5 (class III), chi polypeptide) [NCBI Gene 128]
- **Chemicals:** nitric oxide (PubChem CID 145068)
- **Species:** Aspergillus flavus (taxon 5059)

## Full-text entities

- **Diseases:** carcinogenic (MESH:D011230), fungal (MESH:D009181)
- **Chemicals:** GSNOR (-), ROS (MESH:D017382), Aflatoxin (MESH:D000348), NO (MESH:D009569)
- **Species:** A. flavus [taxon 315677], Aspergillus flavus var. flavus (varietas) [taxon 90340], Aspergillus flavus (species) [taxon 5059], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

44 references — full list in the complete paper: https://tomesphere.com/paper/PMC12838201/full.md

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Source: https://tomesphere.com/paper/PMC12838201