Mingming Chen, Naoyoshi Kumakura, Hironori Saito, Ryan Muller, Madoka Nishimoto, Mari Mito, Pamela Gan, Nicholas T Ingolia, Ken Shirasu, Takuhiro Ito, Yuichi Shichino and Shintaro Iwasaki eLife 12:e81302 (2023)
https://doi.org/10.7554/eLife.81302
Copyright: © 2023
This article is licensed under a Creative Commons Attribution 4.0 International License (CC BY).
Background
Plant-fungus interactions have been extensively studied because fungi infecting plants cause severe crop losses. Plants produce secondary metabolites (such as tannins, terpenoids, saponins, alkaloids, flavonoids, etc.) that can kill fungi as a defense mechanism, while some fungi can detoxify antifungal compounds by secreting certain enzymes. However, little is known about the diversity of mechanisms of plant-fungus competition.
Research Achievements
Under fungal infection, Aglaia plants may have developed rocaglates to target the conserved translation factor eIF4A and to suppress fungal growth. Simultaneously, Aglaia plants exhibit amino acid substitutions in the rocaglate binding pocket of eIF4As to prevent self-poisoning. Some fungi may impede rocaglate toxin by converting eIF4A to a rocaglate-insensitive form, enabling them to parasitize these plants.
A species of fungus, Ophiocordyceps sp. that is able to grow on Aglaia sp. plants despite their production of rocaglates, which are inhibitors of the translation initiation factor (eIF4A), is identified. An amino acid substitution encoded in the fungal eIF4A gene was identified so that rocaglates cannot bind to eIF4A thus preserves eIF4A activity in fungus. This bypass mechanism is similar to the way in which the plant itself bypasses. These results indicate fungal resistance to plant secondary metabolites independent of detoxification enzymes and a unique contest between plants and fungi centered on secondary metabolites synthesized in the host plant.
Use of ProteoSave™ in this Study
ProteoSave 50mL tube was used for conidia culture
- Conidia was incubated on PDA in dark for 6 day
- Conidia generated was suspended in 20 ml of sterilized water.
- Suspension was filtered through a 100 µm pore-size cell strainer
- 20 ml of resuspended conidia at 0.5 OD600 was dispensed in 50 ml ProteoSave SS tube and then treated with aglafoline or DMSO
Use of ProteoSave™ in Fungal Research
Nakamura I, Ohsumi K, Takeda S, Katsumata K, Matsumoto SAkamatsu SMitori H, Nakai T. 2019.
ASP2397 Is a Novel Natural Compound That Exhibits Rapid and Potent Fungicidal Activity against Aspergillus Species through a Specific Transporter. Antimicrob Agents Chemother 63:10.1128/aac.02689-18. https://doi.org/10.1128/aac.02689-18
ProteoSaveTM SS Plate 96F was used in time-kill curve assays to test fungicidal activity.
Cat#: MS-52550Z
Product Name: ProteoSave™ Tube
Material: Body: Polypropylene, Lid: Polyethylene
Sterilization Method: Radiation Sterilization
Package: 5 Tubes/Package, 100 Tubes/case
