期刊
BMC PLANT BIOLOGY
卷 22, 期 1, 页码 -出版社
BMC
DOI: 10.1186/s12870-022-03471-6
关键词
Striga hermonthica; Fusarium oxysporum f; sp; strigae; Fusarium exometabolites; Diacetoxyscirpenol; Biopesticides; Targeted metabolomics; Metabolic footprinting; Trichothecene gene expression
资金
- German Federal Ministry for Economic Cooperation and Development (BMZ)
- German Academic Exchange Service (DAAD)
The study found that the Fusarium exometabolite DAS has strong herbicidal effects on S. hermonthica without affecting the growth of host crops. Incubating DAS in the soil can promote the growth of soil microbial community and degradation of DAS.
Background Certain Fusarium exometabolites have been reported to inhibit seed germination of the cereal-parasitizing witchweed, Striga hermonthica, in vitro. However, it is unknown if these exometabolites will consistently prevent S. hermonthica incidence in planta. The study screened a selection of known, highly phytotoxic Fusarium exometabolites, in identifying the most potent/efficient candidate (i.e., having the greatest effect at minimal concentration) to completely hinder S. hermonthica seed germination in vitro and incidence in planta, without affecting the host crop development and yield. Results In vitro germination assays of the tested Fusarium exometabolites (i.e., 1,4-naphthoquinone, equisetin, fusaric acid, hymeglusin, neosolaniol (Neo), T-2 toxin (T-2) and diacetoxyscirpenol (DAS)) as pre-Striga seed conditioning treatments at 1, 5, 10, 20, 50 and 100 mu M, revealed that only DAS, out of all tested exometabolites, completely inhibited S. hermonthica seed germination at each concentration. It was followed by T-2 and Neo, as from 10 to 20 mu M respectively. The remaining exometabolites reduced S. hermonthica seed germination as from 20 mu M (P < 0. 0001). In planta assessment (in a S. hermonthica-sorghum parasitic system) of the exometabolites at 20 mu M showed that, although, none of the tested exometabolites affected sorghum aboveground dry biomass (P > 0.05), only DAS completely prevented S. hermonthica incidence. Following a 14-d incubation of DAS in the planting soil substrate, bacterial 16S ribosomal RNA (rRNA) and fungal 18S rRNA gene copy numbers of the soil microbial community were enhanced; which coincided with complete degradation of DAS in the substrate. Metabolic footprinting revealed that the S. hermonthica mycoherbicidal agent, Fusarium oxysporum f. sp. strigae (isolates Foxy-2, FK3), did not produce DAS; a discovery that corresponded with underexpression of key genes (Tri5, Tri4) necessary for Fusarium trichothecene biosynthesis (P < 0.0001). Conclusions Among the tested Fusarium exometabolites, DAS exhibited the most promising herbicidal potential against S. hermonthica. Thus, it could serve as a new biocontrol agent for efficient S. hermonthica management. Further examination of DAS specific mode of action against the target weed S. hermonthica at low concentrations (<= 20 mu M), as opposed to non-target soil organisms, is required.
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