Abstract

In this work, we described an in vitro system adequate for investigating the pathosystem soybean/arbuscular mycorrhizal fungi (AMF)/Fusarium virguliforme. Pre-mycorrhized plantlets with Rhizophagus irregularis were infected by F. virguliforme either locally via a plug of gel supporting mycelium (Method 1) or via a macroconidia suspension applied to the medium surface (Method 2). Root colonization by the AMF and infection by the pathogen were similar to the usual observations in pot experiments. Within a period of 18 days, more than 20% of the roots were colonized by the AMF and infection by the pathogen was observed in all the plants. In presence of AMF, a decrease in symptoms and in the level of root tissue infection was noticed. With Method 1, smaller necrotic lesions were observed in the pre-mycorrhized plantlets. In Method 2, pathogen infection was slower but more homogenous. These results demonstrated the suitability of the in vitro cultivation system to study the pathosystem soybean/AMF/F. virguliforme. We propose this in vitro cultivation system for studying the mechanisms involved in the biocontrol conferred by AMF against F. virguliforme in soybean.

Highlights

  • Studies on the belowground plant–microbes interaction have increased tremendously in number and complexity in recent years (Brink, 2016)

  • In the present study we reported and described, for the first time, an in vitro cultivation system associating pre-mycorrhized soybean plantlets infected by F. virguliforme

  • Root colonization by the arbuscular mycorrhizal fungi (AMF) was estimated 96 h (Method 1) and 72 h (Method 2) after inoculation by F. virguliforme. This corresponded to 19 (Method 1) and 18 (Method 2) days postplating of the soybean plantlets in the HC containing the extra-radical mycelium (ERM) of the AMF

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Summary

Introduction

Studies on the belowground plant–microbes interaction have increased tremendously in number and complexity in recent years (Brink, 2016). In the last decades, a number of cultivation systems have been developed to grow them in vitro with root organs (Gutjahr and Parniske, 2013) or whole plants (Voets et al, 2005, 2009; Dupré de Boulois et al, 2006; Koffi et al, 2009). These in vitro systems have allowed the in-deep study of the plant-AMF symbiotic association (Koffi et al, 2013)

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