Nematode-Trapping Fungi Produce Diverse Metabolites during Predator–Prey Interaction

• Main Authors: Ting-Hao Kuo, Ching-Ting Yang, Hsin-Yuan Chang, Yen-Ping Hsueh, Cheng-Chih Hsu
• Format: Article
• Language: English
• Published: MDPI AG 2020-03-01
• Series: Metabolites
• Subjects: nematode-trapping fungi; <i>arthrobotrys</i>; <i>caenorhabditis elegans</i>; predator–prey interaction; metabolomics; molecular networking; <i>arthrobotrys musiformis</i> trap-associated peptide; desferriferrichrome; linoleyl alcohol; nonadecanamide; citicoline
• Online Access: https://www.mdpi.com/2218-1989/10/3/117

Nematode-trapping fungi are natural antagonists of nematodes. These predatory fungi are capable of switching their lifestyle from a saprophytic to predatory stage in the presence of nematodes by developing specialized trapping devices to capture and consume nematodes. The biochemical mechanisms of such predator&#8722;prey interaction have become increasingly studied given the potential application of nematode-trapping fungi as biocontrol agents, but the involved fungal metabolites remain underexplored. Here, we report a comprehensive liquid&#8722;chromatography mass spectrometry (LC&#8722;MS) metabolomics study on one hundred wild isolates of nematode-trapping fungi in three different species, <i>Arthrobotrys</i> <i>oligospora, Arthrobotrys thaumasia</i>, and <i>Arthrobotrys musiformis</i>. Molecular networking analysis revealed that the fungi were capable of producing thousands of metabolites, and such chemical diversity of metabolites was notably increased as the fungi switched lifestyle to the predatory stage. Structural annotations by tandem mass spectrometry revealed that those fungal metabolites belonged to various structural families, such as peptide, siderophore, fatty alcohol, and fatty acid amide, and their production exhibited species specificity. Several small peptides (&lt;1.5 kDa) produced by <i>A.</i> <i>musiformis</i> in the predatory stage were found, with their partial amino acid sequences resolved by the tandem mass spectra. Four fungal metabolites (desferriferrichrome, linoleyl alcohol, nonadecanamide, and citicoline) that were significantly enriched in the predatory stage were identified and validated by chemical standards, and their bioactivities against nematode prey were assessed. The availability of the metabolomics datasets will facilitate comparative studies on the metabolites of nematode-trapping fungi in the future.