Evidence map›Paper›PMID 42207174›Full record

ArticleThe ISME journal2026

CHD-18 g-modulated Pseudomonas taxa support poplar salt tolerance.

Yangwenke Liao, Qingyue Zhang, Jiafeng Zheng, Jinchi Zhang, Tingting Dai, Fuyuan Zhu, Víctor J Carrión, Manuel Delgado-Baquerizo, Christian Sonne, Fuliang Cao and 1 more

Abstract read
In one paragraph

Article in The ISME journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Yangwenke LiaoState Key Laboratory of Tree Genetics and Breeding, Nanjing Forestry University, Nanjing, 210037, Jiangsu, China.ORCID 0000-0002-0676-3477
Qingyue ZhangState Key Laboratory of Tree Genetics and Breeding, Nanjing Forestry University, Nanjing, 210037, Jiangsu, China.
Jiafeng ZhengState Key Laboratory of Tree Genetics and Breeding, Nanjing Forestry University, Nanjing, 210037, Jiangsu, China.
Jinchi ZhangCo-Innovation Center for Sustainable Forestry in Southern China, Nanjing Forestry University, Nanjing, 210037, Jiangsu, China.
Tingting DaiState Key Laboratory of Tree Genetics and Breeding, Nanjing Forestry University, Nanjing, 210037, Jiangsu, China.
Fuyuan ZhuState Key Laboratory of Tree Genetics and Breeding, Nanjing Forestry University, Nanjing, 210037, Jiangsu, China.
Víctor J CarriónDepartamento de Microbiología, Facultad de Ciencias, Campus Universitario de Teatinos s/n, Universidad de Málaga, Málaga, 29010, Málaga, Spain.
Manuel Delgado-BaquerizoLaboratorio de Biodiversidad y Funcionamiento Ecosistémico, Instituto de Recursos Naturales y Agrobiología de Sevilla (IRNAS), CSIC, Sevilla, 41012, Sevilla, Spain.
Christian SonneDepartment of Ecoscience, Aarhus University; Frederiksborgvej 399, Roskilde DK-4000, Zealand, Denmark.
Fuliang CaoState Key Laboratory of Tree Genetics and Breeding, Nanjing Forestry University, Nanjing, 210037, Jiangsu, China.
Xiaogang LiState Key Laboratory of Tree Genetics and Breeding, Nanjing Forestry University, Nanjing, 210037, Jiangsu, China.ORCID 0000-0002-7976-1122

Funding

Jiangsu Special Fund on Technology Innovation of Carbon Dioxide Peaking and Carbon Neutrality BE2022420National Natural Science Foundation of China 32371729National Natural Science Foundation of China 32430069STI 2030 2023ZD0405602
6 · The paper itself

Abstract

Against the background of global climate change, soil salinization has emerged as a major abiotic stressor constraining agroforestry productivity worldwide. Root-recruited microbes enhance plant stress resilience, and host-microbe interactions depend on plant root metabolism. Stress-tolerant plant genotypes exhibit a marked capacity to enrich beneficial root-associated microbes through specialized metabolic responses, thereby facilitating phenotypic plasticity. However, the molecular mechanisms underlying these plant-microbe interactions remain unclear. In this study, we compared salt tolerance among three poplar varieties under aseptic and non-aseptic conditions, and analyzed their rhizosphere bacterial community responses to salt stress. We found that microbial inoculation modulated poplar salt tolerance, and poplar shaped rhizosphere bacterial communities in a genotype-dependent manner. Transcriptome sequencing and targeted metabolomic analysis indicated that salt-tolerant poplar plants preferentially activate the phenylpropanoid biosynthesis pathway, accompanied by the enhanced root secretion of benzoic acid (BA) and salicylic acid (SA) and up-regulation of CHD-18 g encoding cinnamoyl-CoA hydratase/dehydrogenase. Overexpression of CHD-18 g increased rhizosphere Pseudomonas abundance by enhancing BA and SA biosynthesis. Binary interaction assays further showed that the BA-induced Pseudomonas taxa mitigated salt stress and promoted poplar growth under salt stress. Our findings propose a framework linking host gene expression, root metabolism, and key microbial taxa in conferring salt tolerance. This work uncovers a metabolic signaling mechanism by which trees shape their root microbiome to enhance stress adaptation, offering actionable genetic and ecological strategies for improving tree resilience in sustainable agroforestry systems.

Indexed as

Bacterial ProteinsPopulusPseudomonasSalt ToleranceGene Expression ProfilingPlant RootsRhizosphereSoil MicrobiologyStress, PhysiologicalBacterial Proteinscinnamoyl-CoA hydratase/dehydrogenasepoplarPseudomonasroot microbiotasalt stress

Identifiers

PMID42207174
PMCPMC13332713

What Socratic holds

Textmetadata
LicenceCC BY
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Registered trials

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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 Socratic graph.