Evidence map›Paper›PMID 40762940›Full record

ArticleScience China. Life sciences2026

Contribution of orchids to the carbon budget of fungi in germinating seeds of Gymnadenia conopsea.

Yaoyao Wang, Zeyu Zhao, Jiaxin Liu, Aiyiwei Yang, Hans Jacquemyn, Luna Yang, Xin Qian, Taiqiang Li, Gang Ding, Xiaoke Xing

Abstract read
PubMed Publisher
In one paragraph

Article in Science China. Life sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Action Pathways ofPlants (Basel, Switzerland) · 2026
    Article
  5. Review
  6. IMA fungus · 2026
    Article
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

10 authors.

Yaoyao Wang *State Key Laboratory for Quality Ensurance and Sustainable Use of Dao-di Herbs, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100193, China.
Zeyu Zhao *State Key Laboratory for Quality Ensurance and Sustainable Use of Dao-di Herbs, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100193, China.
Jiaxin LiuState Key Laboratory for Quality Ensurance and Sustainable Use of Dao-di Herbs, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100193, China.
Aiyiwei YangState Key Laboratory for Quality Ensurance and Sustainable Use of Dao-di Herbs, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100193, China.
Hans JacquemynDepartment of Biology, Plant Conservation and Population Biology, Katholieke Universiteit Leuven, Leuven, B-3001, Belgium.
Luna YangState Key Laboratory for Quality Ensurance and Sustainable Use of Dao-di Herbs, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100193, China.
Xin QianState Key Laboratory for Quality Ensurance and Sustainable Use of Dao-di Herbs, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100193, China.
Taiqiang LiState Key Laboratory for Quality Ensurance and Sustainable Use of Dao-di Herbs, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100193, China.
Gang DingState Key Laboratory for Quality Ensurance and Sustainable Use of Dao-di Herbs, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100193, China. gding@implad.ac.cn.
Xiaoke XingState Key Laboratory for Quality Ensurance and Sustainable Use of Dao-di Herbs, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100193, China. xkxing2009@hotmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Orchids critically rely on mycorrhizal fungi for seed germination and seedling development, but the extent to which the fungus benefits from the orchid is less clear. Recent work in arbuscular mycorrhizae has suggested that plants can provide fatty acids (FAs) to fungi, but empirical evidence in orchids remains limited. Here, we combine lipidomic and transcriptomic analyses to test the hypothesis that the germination-promoting fungus Ceratobasidium sp. GS2 receives carbon in the form of FAs from Gymnadenia conopsea seeds during symbiotic germination. Confocal and transmission electron microscopy confirmed the potential of FA transfer from seeds to the fungus. Symbiosis resulted in significant changes in the lipid composition of the fungus, with increased concentrations of FAs in the external mycelium. RNA-seq showed upregulation of genes associated with FA synthesis in seeds and downregulation of de novo FA synthesis genes in fungi 12 d post-symbiosis, indicating that the increased amounts of FAs in the fungus may originate from the seeds. These results indicate that FAs absorbed by hyphae in the colonized inner cortex cells support hyphal growth, providing evidence for directional carbon flow from the orchid seeds to the fungus and supporting a "give now and get now" model of mutualism in orchid-fungus symbioses.

Indexed as

BasidiomycotaCarbonGerminationMycorrhizaeOrchidaceaeSeedsFatty AcidsGene Expression ProfilingSymbiosisTranscriptomeCarbonFatty Acidscarbon transferfatty acidsnutrient exchangeorchid mycorrhizasymbiotic seed germination

Identifiers

What Socratic holds

Textmetadata
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Registered trials

None linked

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.