Lipo-Chitooligosaccharides Induce Specialized Fungal Metabolite Profiles That Modulate Bacterial Growth

The activation of silent biosynthetic gene clusters (BGC) for the identification and characterization of novel fungal secondary metabolites is a perpetual motion in natural product discoveries. Here, we demonstrated that one of the best-studied symbiosis signaling compounds, lipo-chitooligosaccharid...

Full description

Saved in:
Bibliographic Details
Published inmSystems Vol. 7; no. 6; pp. e0105222 - 22
Main Authors Rush, Tomás A., Tannous, Joanna, Lane, Matthew J., Gopalakrishnan Meena, Muralikrishnan, Carrell, Alyssa A., Golan, Jacob J., Drott, Milton T., Cottaz, Sylvain, Fort, Sébastien, Ané, Jean-Michel, Keller, Nancy P., Pelletier, Dale A., Jacobson, Daniel A., Kainer, David, Abraham, Paul E., Giannone, Richard J., Labbé, Jesse L.
Format Journal Article
LanguageEnglish
Published United States American Society for Microbiology 01.12.2022
Subjects
Online AccessGet full text
ISSN2379-5077
2379-5077
DOI10.1128/msystems.01052-22

Cover

More Information
Summary:The activation of silent biosynthetic gene clusters (BGC) for the identification and characterization of novel fungal secondary metabolites is a perpetual motion in natural product discoveries. Here, we demonstrated that one of the best-studied symbiosis signaling compounds, lipo-chitooligosaccharides (LCOs), play a role in activating some of these BGCs, resulting in the production of known, putative, and unknown metabolites with biological activities. Lipo-chitooligosaccharides (LCOs) are historically known for their role as microbial-derived signaling molecules that shape plant symbiosis with beneficial rhizobia or mycorrhizal fungi. Recent studies showing that LCOs are widespread across the fungal kingdom have raised questions about the ecological function of these compounds in organisms that do not form symbiotic relationships with plants. To elucidate the ecological function of these compounds, we investigate the metabolomic response of the ubiquitous human pathogen Aspergillus fumigatus to LCOs. Our metabolomics data revealed that exogenous application of various types of LCOs to A. fumigatus resulted in significant shifts in the fungal metabolic profile, with marked changes in the production of specialized metabolites known to mediate ecological interactions. Using network analyses, we identify specific types of LCOs with the most significant effect on the abundance of known metabolites. Extracts of several LCO-induced metabolic profiles significantly impact the growth rates of diverse bacterial species. These findings suggest that LCOs may play an important role in the competitive dynamics of non-plant-symbiotic fungi and bacteria. This study identifies specific metabolomic profiles induced by these ubiquitously produced chemicals and creates a foundation for future studies into the potential roles of LCOs as modulators of interkingdom competition. IMPORTANCE The activation of silent biosynthetic gene clusters (BGC) for the identification and characterization of novel fungal secondary metabolites is a perpetual motion in natural product discoveries. Here, we demonstrated that one of the best-studied symbiosis signaling compounds, lipo-chitooligosaccharides (LCOs), play a role in activating some of these BGCs, resulting in the production of known, putative, and unknown metabolites with biological activities. This collection of metabolites induced by LCOs differentially modulate bacterial growth, while the LCO standards do not convey the same effect. These findings create a paradigm shift showing that LCOs have a more prominent role outside of host recognition of symbiotic microbes. Importantly, our work demonstrates that fungi use LCOs to produce a variety of metabolites with biological activity, which can be a potential source of bio-stimulants, pesticides, or pharmaceuticals.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
AC05-00OR22725; ANR-17-EURE-0003; ANR-15-IDEX-02; CARN-025-01
USDOE Office of Science (SC), Biological and Environmental Research (BER)
French National Research Agency (ANR)
Tomás A. Rush and Joanna Tannous contributed equally. The order of co-author names was decided based on alphabetical order.
The authors declare no conflict of interest.
Present address: Jesse L. Labbé, Invaio Sciences, Cambridge, Massachusetts, USA.
ISSN:2379-5077
2379-5077
DOI:10.1128/msystems.01052-22