Evidence map›Paper›PMID 40960688›Full record

ArticlePlant cell reports2025

Volatile organic compounds from Bacillus velezensis FZB42 remodel Arabidopsis root architecture by an auxin-dependent mechanism.

Ailing Ye, Liang Yue, Andéole Niyongabo Turatsinze, Xiaofan Xie, Zongyu Zhang, Gaofeng Chen, Lingling Wu, Qin Zhou, Yun Wang, Meilan Zhang and 3 more

Abstract read
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In one paragraph

Article in Plant cell reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Journal of bacteriology · 2026
    Review
  2. Article
  3. Plants (Basel, Switzerland) · 2026
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Ailing YeState Key Laboratory of Ecological Safety and Sustainable Development in Arid Lands, Northwest Institute of Eco-Environment and Resources, Chinese Academy of Sciences, Lanzhou 730000, China.
Liang YueState Key Laboratory of Ecological Safety and Sustainable Development in Arid Lands, Northwest Institute of Eco-Environment and Resources, Chinese Academy of Sciences, Lanzhou 730000, China.
Andéole Niyongabo TuratsinzeState Key Laboratory of Ecological Safety and Sustainable Development in Arid Lands, Northwest Institute of Eco-Environment and Resources, Chinese Academy of Sciences, Lanzhou 730000, China.
Xiaofan XieState Key Laboratory of Ecological Safety and Sustainable Development in Arid Lands, Northwest Institute of Eco-Environment and Resources, Chinese Academy of Sciences, Lanzhou 730000, China.
Zongyu ZhangState Key Laboratory of Ecological Safety and Sustainable Development in Arid Lands, Northwest Institute of Eco-Environment and Resources, Chinese Academy of Sciences, Lanzhou 730000, China.
Gaofeng ChenGansu Shangnong Biotechnology Co. Ltd, Baiyin 730900, China.
Lingling WuState Key Laboratory of Ecological Safety and Sustainable Development in Arid Lands, Northwest Institute of Eco-Environment and Resources, Chinese Academy of Sciences, Lanzhou 730000, China.
Qin ZhouState Key Laboratory of Ecological Safety and Sustainable Development in Arid Lands, Northwest Institute of Eco-Environment and Resources, Chinese Academy of Sciences, Lanzhou 730000, China.
Yun WangState Key Laboratory of Ecological Safety and Sustainable Development in Arid Lands, Northwest Institute of Eco-Environment and Resources, Chinese Academy of Sciences, Lanzhou 730000, China.
Meilan ZhangState Key Laboratory of Ecological Safety and Sustainable Development in Arid Lands, Northwest Institute of Eco-Environment and Resources, Chinese Academy of Sciences, Lanzhou 730000, China.
Yubao ZhangState Key Laboratory of Ecological Safety and Sustainable Development in Arid Lands, Northwest Institute of Eco-Environment and Resources, Chinese Academy of Sciences, Lanzhou 730000, China.
Jiecai ZhaoState Key Laboratory of Ecological Safety and Sustainable Development in Arid Lands, Northwest Institute of Eco-Environment and Resources, Chinese Academy of Sciences, Lanzhou 730000, China.
Ruoyu WangState Key Laboratory of Ecological Safety and Sustainable Development in Arid Lands, Northwest Institute of Eco-Environment and Resources, Chinese Academy of Sciences, Lanzhou 730000, China. wangruoyu@lzb.ac.cn.ORCID http://orcid.org/0000-0002-8043-1139

Funding

Pilot Project on Comprehensive Utilisation of Saline and Alkaline Land in Jingtai County, Baiyin City, Gansu Province - (Section II) Core Pilot Demonstration Projec JTYJDSDXM-SG-02the Global Common Challenges Project of the International Partnership Program of Chinese Academy of Sciences 315GJHZ2024123GC
6 · The paper itself

Abstract

key messageVolatile organic compounds produced by plant growth-promoting rhizobacteria promote lateral root development by modulating the auxin signaling pathway in Arabidopsis thaliana, thereby remodeling root architecture. Volatile organic compounds (VOCs) emitted by plant growth-promoting rhizobacteria (PGPR) have been shown to promote both shoot and root growth in plants. While VOCs are known to modulate root architecture, the underlying mechanisms remain poorly understood. In this study, we demonstrate that VOCs released by Bacillus velezensis FZB42 significantly promote primary root elongation and increase lateral root (LR) development in Arabidopsis thaliana, thereby altering root architecture. This study indicates that VOC-mediated modulation of root architecture is closely associated with auxin signaling, particularly its polar transport. Notably, the promotive effects of VOCs on lateral root formation were nearly abolished in auxin signaling mutants, including pin2 and axr1-12. Our results further demonstrate that treatment with FZB42-VOCs does not rescue the lateral root deficiency phenotype in the auxin core components arf7 arf19 double mutants. VOCs were found to stimulate the emergence of lateral root primordia (LRP) and to induce the expression of the auxin-responsive marker DR5:GFP in pre-existing LRPs. Additionally, VOCs were found to modulate the expression of auxin efflux carriers, such as PIN1 and PIN2, and to induce DR5:GFP expression in both primary and lateral roots. Treatment with NPA, an auxin transport inhibitor, further confirmed that VOC-mediated remodeling of root architecture is dependent on auxin polar transport. In conclusion, these findings suggest that VOCs enhance auxin response during early lateral root development by modulating auxin distribution and downstream signaling, thereby stimulating lateral root formation. These findings provide valuable insights into microbe-mediated root development and could inform sustainable agricultural practices involving PGPR.

Indexed as

ArabidopsisBacillusIndoleacetic AcidsPlant RootsVolatile Organic CompoundsArabidopsis ProteinsGene Expression Regulation, PlantMutationPlant Growth RegulatorsSignal TransductionArabidopsis ProteinsIndoleacetic AcidsPlant Growth RegulatorsVolatile Organic CompoundsArabidopsis thalianaAuxin polar transportBacillus velezensisRoot architectureVOC

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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.