Evidence map›Paper›PMID 41419732›Full record

ArticleNature communications2025

Humidity-driven ABA depletion determines plant-pathogen competition for leaf water.

Shigetaka Yasuda, Akihisa Shinozawa, Yuanjie Weng, Arullthevan Rajendram, Taishi Hirase, Haruka Ishizaki, Ryuji Suzuki, Shioriko Ueda, Rahul Sk, Yumiko Takebayashi and 4 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Cellular energy sensor SnRK1 suppresses salicylic acid-dependent and -independent defenses and bacterial resistance inProceedings of the National Academy of Sciences of the United States of America · 2025
    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

14 authors.

Shigetaka YasudaGraduate School of Science and Technology, Nara Institute of Science and Technology, Ikoma, Japan. shige-yasuda@bs.naist.jp.ORCID http://orcid.org/0000-0002-4602-6404
Akihisa Shinozawa *Department of Bioscience, Tokyo University of Agriculture, Tokyo, Japan.
Yuanjie Weng *Center for Sustainable Resource Science, RIKEN, Yokohama, Japan.
Arullthevan Rajendram *Graduate School of Science and Technology, Nara Institute of Science and Technology, Ikoma, Japan.
Taishi Hirase *Graduate School of Science and Technology, Nara Institute of Science and Technology, Ikoma, Japan.
Haruka IshizakiGraduate School of Science and Technology, Nara Institute of Science and Technology, Ikoma, Japan.
Ryuji SuzukiDepartment of Biochemistry and Molecular Biology, Saitama University, Saitama, Japan.
Shioriko UedaGraduate School of Science and Technology, Nara Institute of Science and Technology, Ikoma, Japan.
Rahul SkThe NODAI Genome Research Center (NGRC), Tokyo University of Agriculture, Tokyo, Japan.ORCID http://orcid.org/0000-0002-0521-9162
Yumiko TakebayashiCenter for Sustainable Resource Science, RIKEN, Yokohama, Japan.ORCID http://orcid.org/0000-0003-4207-297X
Izumi YotsuiDepartment of Bioscience, Tokyo University of Agriculture, Tokyo, Japan.
Masatsugu ToyotaDepartment of Biochemistry and Molecular Biology, Saitama University, Saitama, Japan.ORCID http://orcid.org/0000-0002-9544-0978
Masanori OkamotoCenter for Sustainable Resource Science, RIKEN, Yokohama, Japan.ORCID http://orcid.org/0000-0002-1743-0408
Yusuke SaijoGraduate School of Science and Technology, Nara Institute of Science and Technology, Ikoma, Japan. saijo@bs.naist.jp.ORCID http://orcid.org/0000-0001-8985-9695

Funding

Institute for Fermentation, Osaka (IFO) G-2025-2-089MEXT | Japan Science and Technology Agency (JST) JPMJAX22BNMEXT | Japan Society for the Promotion of Science (JSPS) 21H02507MEXT | Japan Society for the Promotion of Science (JSPS) 21K14829MEXT | Japan Society for the Promotion of Science (JSPS) 24H00565MEXT | JST | Exploratory Research for Advanced Technology (ERATO) JPMJER2403
6 · The paper itself

Abstract

Bacterial phytopathogens, such as Pseudomonas syringae pv. tomato (Pst) DC3000, induce water-soaked lesions in the leaf apoplast under high humidity, facilitating infection. However, it remains largely unclear how plants regulate their resistance to restrict bacterial infection in response to humidity. Here, we demonstrate that abscisic acid (ABA)-catabolizing ABA 8'-hydroxylase, encoded by CYP707A3, plays a critical role in this resistance in Arabidopsis thaliana. Elevated humidity induces CYP707A3 expression, which is essential for reducing ABA levels and promoting stomatal opening, thereby limiting bacterial water-soaking and infection following leaf invasion. High humidity also increases cytosolic Ca

Indexed as

Abscisic AcidArabidopsisHumidityPlant DiseasesPlant LeavesPseudomonas syringaeWaterArabidopsis ProteinsCalciumCalcium ChannelsCytochrome P-450 Enzyme SystemDisease ResistanceGene Expression Regulation, PlantHost-Pathogen InteractionsPlant ProteinsPlant StomataAbscisic Acidabscisic acid 8'-hydroxylaseArabidopsis ProteinsCalciumCalcium ChannelsCytochrome P-450 Enzyme SystemPlant ProteinsWater

Identifiers

PMID41419732
PMCPMC12824301

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.