Abstract

Fungal co-cultivation has emerged as a promising way for activating cryptic biosynthetic pathways and discovering novel antimicrobial metabolites. For the success of such studies, a key element remains the development of standardized co-cultivation methods compatible with high-throughput analytical procedures. To efficiently highlight induction processes, it is crucial to acquire a holistic view of intermicrobial communication at the molecular level. To tackle this issue, a strategy was developed based on the miniaturization of fungal cultures that allows for a concomitant survey of induction phenomena in volatile and non-volatile metabolomes. Fungi were directly grown in vials, and each sample was profiled by head space solid phase microextraction gas chromatography mass spectrometry (HS-SPME-GC-MS), while the corresponding solid culture medium was analyzed by liquid chromatography high resolution mass spectrometry (LC-HRMS) after solvent extraction. This strategy was implemented for the screening of volatile and non-volatile metabolite inductions in an ecologically relevant fungal co-culture of Eutypa lata (Pers.) Tul. & C. Tul. (Diatrypaceae) and Botryosphaeria obtusa (Schwein.) Shoemaker (Botryosphaeriaceae), two wood-decaying fungi interacting in the context of esca disease of grapevine. For a comprehensive evaluation of the results, a multivariate data analysis combining Analysis of Variance and Partial Least Squares approaches, namely AMOPLS, was used to explore the complex LC-HRMS and GC-MS datasets and highlight dynamically induced compounds. A time-series study was carried out over 9 days, showing characteristic metabolite induction patterns in both volatile and non-volatile dimensions. Relevant links between the dynamics of expression of specific metabolite production were observed. In addition, the antifungal activity of 2-nonanone, a metabolite incrementally produced over time in the volatile fraction, was assessed against Eutypa lata and Botryosphaeria obtusa in an adapted bioassay set for volatile compounds. This compound has shown antifungal activity on both fungi and was found to be co-expressed with a known antifungal compound, O-methylmellein, induced in solid media. This strategy could help elucidate microbial inter- and intra-species cross-talk at various levels. Moreover, it supports the study of concerted defense/communication mechanisms for efficiently identifying original antimicrobials.

Highlights

  • It is well established that microbial natural products (NPs) represent one of the most important resources for the discovery of potent antimicrobials (Koehn and Carter, 2005; Newman and Cragg, 2016).Finding new antimicrobial agents remains key in fighting pathogens for both human health and agronomical needs, to address the challenge related to resistance phenomena

  • We previously showed that a miniaturization of co-culture experiments on solid media is well adapted for acquiring fast metabolite fingerprints of large number of replicates needed for time-series metabolomic investigations

  • A strategy based on the cultivation of fungal single cultures and co-cultures in solid phase microextraction (SPME) vial was developed to study the evolution of volatile and non-volatile metabolite induction at four different time points (2, 4, 7, and 9 days) in a fungal co-culture of Eutypa lata and Botryosphaeria obtusa

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Summary

Introduction

In this study, we developed a miniaturized procedure for a concomitant analysis of the volatile and non-volatile fractions of the same microbial co-culture by metabolomics in time-series experiments. A strategy was developed and applied to reveal the induction of volatile and non-volatile metabolites over time in an ecologically relevant fungal co-culture of two wood-decaying fungi interacting in the context of esca disease of grapevine (Eutypa lata and Botryosphaeria obtusa) (Glauser et al, 2009; Hofstetter et al, 2012).

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