# Diversity, climatic correlations, and biocontrol prospects of seed-borne fungal endophytes in Egyptian maize

**Authors:** Khadiga A. Hasan, Hoda M. Soliman, Khalid M. Ghoneem, Yasser M. Shabana

PMC · DOI: 10.1038/s41598-026-41567-3 · 2026-03-26

## TL;DR

This study explores the fungal communities in Egyptian maize seeds and their climate-related patterns, identifying a promising natural biocontrol agent against a harmful fungus.

## Contribution

The study identifies a core group of seed-borne fungi in Egyptian maize and evaluates a native Trichoderma isolate as a potential biocontrol agent.

## Key findings

- A total of 34 endophytic fungal species from 23 genera were identified in Egyptian maize seeds.
- Trichoderma longibrachiatum (T14) inhibited Fusarium verticillioides growth by 74.03% in vitro.
- Climate factors like temperature, solar radiation, and humidity explained 63.6% of fungal community variation.

## Abstract

Maize (Zea mays L.) is the world’s third most important cereal crop, valued for its roles in human food, animal feed, industrial products, and biofuels. Its seeds harbor diverse endophytic fungi that can affect seed quality, plant health, and resilience. Given the vertical transmission of seed microbiota, this study investigated the diversity of seed-borne fungal endophytes in Egyptian maize cultivars across 18 governorates and assessed their associations with regional climate. In addition, the study evaluated the antagonistic activity of native Trichoderma isolates as potential biocontrol agents against Fusarium verticillioides, a major seed-borne pathogen threatening maize production. A total of 34 endophytic fungal species from 23 genera were identified. Aspergillus niger, Penicillium spp., A. flavus, and F. verticillioides were the most prevalent, with A. niger occurring in 97.2% of sites and F. verticillioides in 89.6%. Relative abundances were highest for Penicillium spp. (20.08%), A. niger (18.15%), and F. verticillioides (14.93%). Diversity metrics varied regionally, with species richness ranging from 8 to 22 and Shannon diversity indices (H) from 1.02 to 2.46. Canonical correspondence analysis revealed that temperature, solar radiation, and humidity collectively explained 63.6% of fungal community variation. Trichoderma longibrachiatum (T14) demonstrated the strongest antagonistic effect, inhibiting F. verticillioides growth by 74.03% in vitro and exhibiting pronounced mycoparasitic features. This study highlights the dominance of a core group of seed-borne endophytes in Egyptian maize and underscores the significant role of climate in structuring fungal communities. However, as this study was based on single-season, culture-dependent data with limited molecular validation, further multi-seasonal and molecular-based investigations are needed to confirm these patterns and fully characterize the maize seed mycobiome. Notably, T. longibrachiatum demonstrated strong biocontrol potential against F. verticillioides, offering promise as a native, eco-friendly biocontrol agent for maize production systems in semi-arid environments.

The online version contains supplementary material available at 10.1038/s41598-026-41567-3.

## Linked entities

- **Species:** Zea mays (taxon 4577), Fusarium verticillioides (taxon 117187), Trichoderma longibrachiatum (taxon 5548), Aspergillus niger (taxon 5061)

## Full-text entities

- **Diseases:** fungal (MESH:D009181), ear and stalk infections (MESH:D010031), rot (MESH:D005535), toxicity (MESH:D064420)
- **Chemicals:** ethanol (MESH:D000431), agarose (MESH:D012685), 1-octyn-3-ol (-), tebuconazole (MESH:C087114), palladium (MESH:D010165), phosphate (MESH:D010710), osmium tetroxide (MESH:D009993), water (MESH:D014867), trifloxystrobin (MESH:C467051), agar (MESH:D000362), fumonisin (MESH:D037341), gold (MESH:D006046), NaOCl (MESH:D012973), MgCl2 (MESH:D015636), glutaraldehyde (MESH:D005976), sucrose (MESH:D013395), sodium phosphate (MESH:C018279), paraformaldehyde (MESH:C003043), prochloraz (MESH:C045362), FB1 (MESH:C056933)
- **Species:** Aspergillus ochraceus (species) [taxon 40380], Trichoderma harzianum (species) [taxon 5544], Vigna unguiculata (cowpea, species) [taxon 3917], Curvularia lunata (species) [taxon 5503], Penicillium (genus) [taxon 5073], Aspergillus flavus (species) [taxon 5059], Chaetomium (genus) [taxon 5149], Hapsidospora chrysogena (species) [taxon 5044], Trichoderma hamatum (species) [taxon 49224], Trichoderma (genus) [taxon 5543], Aspergillus niger (species) [taxon 5061], Oryza sativa (Asian cultivated rice, species) [taxon 4530], Aspergillus tamarii (species) [taxon 41984], Hanseniaspora sp. Aw (species) [taxon 544724], Curvularia hawaiiensis (species) [taxon 1230527], Zea mays (maize, species) [taxon 4577], Fusarium pseudograminearum (species) [taxon 101028], Fusarium oxysporum (species) [taxon 5507], Aureobasidium pullulans (species) [taxon 5580], Trichoderma atroviride (species) [taxon 63577], Cladosporium (genus) [taxon 5498], Botrytis cinerea (gray fruit mold, species) [taxon 40559], Fusarium verticillioides (species) [taxon 117187], Arachis hypogaea (goober, species) [taxon 3818], Fungi (kingdom) [taxon 4751], Aspergillus glaucus (species) [taxon 41413], Sorghum bicolor (broomcorn, species) [taxon 4558], Homo sapiens (human, species) [taxon 9606], Rhizopus stolonifer (species) [taxon 4846], Alternaria alternata (species) [taxon 5599], Fusarium solani (species) [taxon 169388], Trichoderma longibrachiatum (species) [taxon 5548], Aspergillus clavatus (species) [taxon 5057], Mycosarcoma maydis (corn smut, species) [taxon 5270], Aspergillus fumigatus (species) [taxon 746128], Rhizoctonia solani (species) [taxon 456999], Fusarium incarnatum (species) [taxon 298378], A. flavus [taxon 315677]

## Figures

13 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13031278/full.md

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Source: https://tomesphere.com/paper/PMC13031278