Lipo-chitooligosaccharides (LCOs) are signaling molecules produced by rhizobial bacteria that trigger the nodulation process in legumes, and by some fungi that also establish symbiotic relationships with plants, notably the arbuscular and ecto mycorrhizal fungi. Here, we show that many other fungi also produce LCOs. We tested 59 species representing most fungal phyla, and found that 53 species produce LCOs that can be detected by functional assays and/or by mass spectroscopy. LCO treatment affects spore germination, branching of hyphae, pseudohyphal growth, and transcription in non-symbiotic fungi from the Ascomycete and Basidiomycete phyla. Our findings suggest that LCO production is common among fungi, and LCOs may function as signals regulating fungal growth and development.
Bibliographical noteFunding Information:
We thank Dr. Hugues Driguez for providing some synthetic lipochitin standards for mass spectrometry. RNA-Seq data were based upon work supported by the National Science Foundation under Award Numbers DBI-0735191, DBI-1265383, and DBI-1743442 (URL: http://www.cyverse.org). Support for mass spectrometry analyses was provided by the ICT-Mass spectrometry and MetaToul-MetaboHUB Facilities, and by the MetaboHUB-ANR-11-INBS-0010 network. Support for synthesis and characterization of COs and LCOs was provided by Labex Arcane and CBH-EUR-GS (ANR-17-EURE-0003), CDP Glyco@alps (ANR-15-IDEX-02), PolyNat Carnot Institut (16-CARN-0025-01), and ICMG (FR 2607) mass spectrometry platform. We thank Dr. Gregory Bonito for the cultures of Mortierella elongata, M. minutissima, and Mortierella sp. nov. strain GBAus27b; Dr. Tony Goldberg, Dr. Jeffrey Lorch, and Karen Vanderwolf for cultures of Aureobasidium pullulans, Protomyces inouye, R. mucilaginosa, and Taphrina virginica; Dr. Chris Hittinger for a culture of S. cerevisiae; Dr. Brian Hudelson and Armila Francis for cultures of Fusarium oxysporum, Mucor circinelloides, P. ery-throseptica, P. ultimum, and Trichoderma harizanum; Dr. Paul Koch for cultures of Clarireedia homoeocarpa, Fusarium fujikuroi, and Typhula incarnata; Drs. Timothy James and Rabern Simmons for cultures of Entophlyctis luteolus, Paraphysoderma sedebokerensis, and Powellomyces hirtus; Dr. Thierry Rouxel for a culture of L. maculans; Drs. Francis Martin and Annegret Kohler for their advice and for cultures of L. bicolor, C. geophilum, G. stellatum, and L. palutris; and Dr. Anne Pringle for cultures and samples of Amanita muscaria and A. thiersii. We also thank Marie Rodriguez, Juliette Teyssandier, Clément Bertrand, and Sandrine Paute for technical assistance, and Drs. Jacob Golan and Katie Morey Gold for statistical advice. This work was supported by the French Agence Nationale de la Recherche under contract ANR-14-CE18-0008-01, the research project Engineering Nitrogen Symbiosis for Africa (ENSA), which is funded through a grant to the University of Cambridge by the Bill & Melinda Gates Foundation (OPP11772165), the Laboratoire d’Excellence entitled TULIP (ANR-10-LABX-41), the Plant-Microbe Interfaces Scientific Focus Area in the Genomic Science Program, the Office of Biological and Environmental Research in the US Department of Energy (DOE) Office of Science (Oak Ridge National Laboratory is managed by UT-Battelle, LLC, the DOE (contract DE-AC05-00OR22725), the United States Department of Agriculture (WIS01695), and by the National Science Foundation (DGE-1256259, PGRP −1546742, and IOS-1331098). We thank the University of Wisconsin-Madison Advanced Opportunity Fellowship, Science, and Medicine Graduate Research Scholars program and the Ford Foundation Pre-Doctoral Scholarship for their support and funding of T.A. Rush.
© 2020, The Author(s).
PubMed: MeSH publication types
- Journal Article
- Research Support, Non-U.S. Gov't
- Research Support, U.S. Gov't, Non-P.H.S.