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Rigerte, L.

Publications and source records attributed to Rigerte, L..

2 recordsLinked to original sources

The induction of systemic resistance to barley powdery mildew by rhizosphere bacterial communities does not disrupt the structure or function of native microbial communities

1.Synthetic microbial communities (SynComs) could help plants withstand biotic stress and reduce the need for pesticides. With this in mind, we created two SynComs, comprising bacterial strains isolated from the rhizospheres of barley and wheat. We then studied their potential to trigger induced systemic resistance against the barley pathogen Blumeria graminis f. sp. hordei (Bgh). To investigate the plant-microbial interactions from the perspective of both plants and microbes, we performed DAF staining to quantify Bgh propagation in plant leaves, analysed leaf transcriptomes and conducted rhizosp here 16S rRNA gene metabarcoding and rhizosphere metatranscriptome analysis. Our results demonstrate that the SynComs elicit defence responses in barley against Bgh in a manner similar to that of the positive control strain Pseudomonas simiae WCS417r. The SynComs act without triggering a strong gene response prior to inoculation with the plant pathogen or affecting plant-associated prokaryote communities; they only mildly influence bacterial gene expression in the rhizosphere. Instead, they act as priming agents, preparing the plant for further pathogen attack. These findings suggest that protective SynComs can be applied in the field without causing signficant disruption to native microbial communities.

microbiology↗

Genetic factors driving multi-host infection in a core member of the root mycobiota

Core members of the fungal root microbiota include pathogens capable of colonizing multiple hosts, yet the underlying genetic determinants remain unknown. We report that Plectosphaerella cucumerina is a core member of the Arabidopsis thaliana root microbiota displaying high pathogenic potential and multi-host colonization capabilities. Establishment of a Plectosphaerella reference culture collection, followed by whole-genome sequencing of 72 strains reveals subtle phenotypic and genotypic variation that associate with fungal phylogeny, but not host plant identity. Transcriptome profiling of a model P. cucumerina isolate in roots of multiple hosts identifies core and host-specific fungal processes linked to carbon catabolism and root cell wall deconstruction of the hosts. A fungal gene encoding a candidate {beta}-1,3-glucanase (GH64) was identified as a key genetic factor driving infection and disease in plants that diverged 110 million years ago. The gene is enriched in plant-colonizing fungi and consistently functions as a disease determinant in the root pathogen Colletotrichum incanum. We conclude that diverse and tunable fungal repertoires of carbohydrate-active enzymes act as disease determinants and drive multi-host compatibility belowground.

microbiology↗