ArticleCommunications biology2022
Selection pressure on the rhizosphere microbiome can alter nitrogen use efficiency and seed yield in Brassica rapa.
Article in Communications biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed.
- Review
- Copper-sensitive OsSPL9 TF regulates expression of indica rice domestication-associated miRNAs and phenotypes.Communications biology · 2026Article
- Adaptive laboratory evolution enhances cell yield and lipid production ofFrontiers in microbiology · 2025Article
- Rhizosphere microbiomes derived from vermicompost alter gene expression and regulatory pathways in tomato (Solanum lycopersicum, L.).Scientific reports · 2024Article
- Implications of bacteria‒bacteria interactions within the plant microbiota for plant health and productivity.Journal of Zhejiang University. Science. B · 2024Review
- Rational management of the plant microbiome for the Second Green Revolution.Plant communications · 2024Review
- Selection pressure on the rhizosphere microbiome can alter nitrogen use efficiency and seed yield in Brassica rapa.Communications biology · 2022Article
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Authors and funding
8 authors.
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Abstract
Microbial experimental systems provide a platform to observe how networks of groups emerge to impact plant development. We applied selection pressure for microbiome enhancement of Brassica rapa biomass to examine adaptive bacterial group dynamics under soil nitrogen limitation. In the 9th and final generation of the experiment, selection pressure enhanced B. rapa seed yield and nitrogen use efficiency compared to our control treatment, with no effect between the random selection and control treatments. Aboveground biomass increased for both the high biomass selection and random selection plants. Soil bacterial diversity declined under high B. rapa biomass selection, suggesting a possible ecological filtering mechanism to remove bacterial taxa. Distinct sub-groups of interactions emerged among bacterial phyla such as Proteobacteria and Bacteroidetes in response to selection. Extended Local Similarity Analysis and NetShift indicated greater connectivity of the bacterial community, with more edges, shorter path lengths, and altered modularity through the course of selection for enhanced plant biomass. In contrast, bacterial communities under random selection and no selection showed less complex interaction profiles of bacterial taxa. These results suggest that group-level bacterial interactions could be modified to collectively shift microbiome functions impacting the growth of the host plant under soil nitrogen limitation.
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