ArticlemBio2026
Rare taxa modulate the emergence of dominants in microbial communities.
Article in mBio, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
3 citing papers in PubMed.
- Nordic Walking Combined with Time-Restricted Eating Is Associated with Changes in Gut Microbiota Composition in Adults with Obesity-Pilot Study.Nutrients · 2026Article
- Common genetic variants in vitamin D metabolism-related genes affect gut microbiota diversity in postmenopausal women.Genes & nutrition · 2026Article
- Roles of microbial interactions in determining the establishment and function of synthetic consortium inoculants for soil applications.The ISME journal · 2025Article
Corrections and comments
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Microbial communities typically comprise a few dominant taxa alongside numerous rare members. While dominant formation is generally attributed to species-level traits that confer adaptation to specific environments, it remains unclear how the rare biosphere influences which taxa ultimately become dominant. We constructed thousands of sub-communities from a soil microbiome using appropriate dilution to preserve the dominants but allow stochastic variation in rare assemblages. Following cultivation under an identical growth condition, dominant taxa varied substantially across replicates, which were determined to be driven primarily by species generalist competitive capacities rather than their initial relative abundances. Notably, the identity of the most abundant taxon in each sub-community was modulated by interactions with rare community members. Co-occurrence and metabolic resource overlap analyses revealed predominantly negative interactions among dominant taxa, while rare taxa exhibited variable and asymmetric interaction patterns. A refined consumer-resource model supported these observations, showing that species are first "nominated" as dominant candidates based on generalist competitive capacities, and then "voted" into the most abundant taxon in a community through collective feedback from rare taxa. The findings imply that dominant emergence in microbial communities is not solely determined by intrinsic species traits but is also critically shaped by interactions with rare taxa. The proposed "nomination-voting" model highlights a collective role of the rare biosphere in shaping community structure and offers a new framework for understanding microbial assembly.IMPORTANCEMicrobial ecosystems are almost always dominated by only a few species, but their diversity resides in the rare biosphere. These rare members are usually considered passive passengers with little influence, yet our work reveals that they can collectively determine which species to become the most abundant taxon. We describe this process as a "nomination-voting" system: competitive traits nominate potential dominants, while rare taxa vote for the ultimate winner through their complex interactions. Recognizing this hidden but decisive role of rare microbes provides a new perspective on community assembly and underscores how subtle ecological interactions shape community outcomes. This assembly framework offers new opportunities for the prediction, manipulation, and stabilization of agriculture, health, and environmental microbiomes.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.