Microbial volatile organic compounds (VOCs) mediate rhizosphere plant-microbe interactions, yet their integrated effects on plant microbiome assembly and host transcriptional regulation remain unresolved. Here we address this gap by investigating how two common VOCs, acetoin (AC) and 2,3-butanediol (BD), influence growth, rhizosphere communities, and root gene expression in the medicinal plant Pseudostellaria heterophylla using a split-pot system. Bacterial and fungal communities were monitored across three developmental stages via amplicon sequencing, alongside root transcriptome profiling during tuber enlargement. Contrasting with widely reported growth-promoting effects of microbial VOCs, both compounds significantly reduced tuber number and biomass. Bacterial communities remained taxonomically stable, shaped primarily by species replacement, with modest VOC responses but clear shifts across developmental stages. Fungal communities exhibited marked compositional restructuring and greater treatment sensitivity, particularly under BD. Neutral community modeling indicated predominantly stochastic bacterial assembly, while fungal assembly—especially under BD—showed stronger influence of deterministic processes. BD associated with broader transcriptional reprogramming than AC, including downregulation of photosynthesis, specialized metabolism, and defense pathways. Cross-omics network analysis revealed discriminant genera (e.g., Granulicella, Harposporium) that correlated strongly with host genes involved in stress response, development, and epigenetic regulation, with fungal taxa showing tighter associations with host expression than bacteria. Together, these findings establish a mechanistic framework for how microbial VOCs shape rhizosphere communities and host responses, with implications for microbiome-based strategies in medicinal plant cultivation.
Yang et al. (Sat,) studied this question.