Hordeum vulgare differentiates its response to beneficial bacteria

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Background
In nature, beneficial bacteria triggering induced systemic resistance (ISR) may protect plants from potential diseases, reducing yield losses caused by diverse pathogens. However, little is known about how the host plant initially responds to different beneficial bacteria. To reveal the impact of different bacteria on barley (Hordeum vulgare), bacterial colonization patterns, gene expression, and composition of seed endophytes were explored.

Results
This study used the soil-borne Ensifer meliloti, as well as Pantoea sp. and Pseudomonas sp. isolated from barley seeds, individually. The results demonstrated that those bacteria persisted in the rhizosphere but with different colonization patterns. Although root-leaf translocation was not observed, all three bacteria induced systemic resistance (ISR) against foliar fungal pathogens. Transcriptome analysis revealed that ion- and stress-related genes were regulated in plants that first encountered bacteria. Iron homeostasis and heat stress responses were involved in the response to E. meliloti and Pantoea sp., even if the iron content was not altered. Heat shock protein-encoding genes responded to inoculation with Pantoea sp. and Pseudomonas sp. Furthermore, bacterial inoculation affected the composition of seed endophytes. Investigation of the following generation indicated that the enhanced resistance was not heritable.

Conclusions
Here, using barley as a model, we highlighted different responses to three different beneficial bacteria as well as the influence of soil-borne Ensifer meliloti on the seed microbiome. In total, these results can help to understand the interaction between ISR-triggering bacteria and a crop plant, which is essential for the application of biological agents in sustainable agriculture.
OriginalsprogEngelsk
Artikelnummer460
TidsskriftBMC Plant Biology
Vol/bind23
Udgave nummer1
Antal sider16
ISSN1471-2229
DOI
StatusUdgivet - 2023

Bibliografisk note

Funding Information:
The authors thank Maximilien Beuret for the ICP-MS analysis performed in the Pôle de Compétences Chimie Analytique Environnementale, ANATELo, LIEC laboratory, UMR 7360 CNRS – Université de Lorraine. We acknowledge Kornelia Smalla for discussion on this manuscript. The figures were created with the help of BioRender.

Funding Information:
This work was supported by the Federal Ministry of Education and Research (BMBF), Projektträger Jülich (PtJ), PrimedPlant-2 project [grant number 031B0886B to A. S.] and China Scholarship Council (CSC) [grant numbers 201806350041 to Y. D., grant numbers 201906350038 to M. H.] Figures were prepared with the help of BioRender.

Publisher Copyright:
© 2023, BioMed Central Ltd., part of Springer Nature.

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