Evidence map›Paper›PMID 41331556›Full record

ArticleBMC plant biology2025

CaSBP12 is implicated in pepper's defense resistance to Phytophthora capsici infection associated with the SA signaling pathway.

Huai-Xia Zhang, Shuang Wu, Yu-Ting Yang, Abid Khan, Chun-Hui Wu, Fei-Fei Pan, Bi-Hua Chen, Xin-Zheng Li, Bing Hu, Zhen-Hui Gong

Abstract read
In one paragraph

Article in BMC plant biology, 2025. 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

10 authors.

Huai-Xia ZhangCollege of Horticulture and Landscape Architecture, Henan Institute of Science and Technology, Xinxiang, Henan, P.R. China.
Shuang WuCollege of Horticulture and Landscape Architecture, Henan Institute of Science and Technology, Xinxiang, Henan, P.R. China.
Yu-Ting YangSchool of Wine & Horticulture, Ningxia University, Yinchuan, 715100, China.
Abid KhanDepartment of Horticulture, The University of Haripur, Haripur, 22620, Pakistan.
Chun-Hui WuCollege of Horticulture and Landscape Architecture, Henan Institute of Science and Technology, Xinxiang, Henan, P.R. China.
Fei-Fei PanCollege of Horticulture and Landscape Architecture, Henan Institute of Science and Technology, Xinxiang, Henan, P.R. China.
Bi-Hua ChenCollege of Horticulture and Landscape Architecture, Henan Institute of Science and Technology, Xinxiang, Henan, P.R. China.
Xin-Zheng LiCollege of Horticulture and Landscape Architecture, Henan Institute of Science and Technology, Xinxiang, Henan, P.R. China.
Bing HuHenan Provincial Agricultural and Rural Science and Technology Education Center, Zhengzhou, China.
Zhen-Hui GongCollege of Horticulture, Northwest A&F University, No.3 TaichengRoad, Yangling, Shaanxi, 712100, P. R. China. zhgong@nwafu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPepper is a crucial vegetable crop with significant economic value, yet its yield and quality are severely affected by pepper Phytophthora Blight. Our previous research indicated that CaSBP12 negatively regulates pepper resistance to Phytophthora capsici (P. capsici) infection. However, the precise role of CaSBP12 in the defense response against P. capsici remains unclear. Thus, it is essential to investigate the defense mechanisms by which CaSBP12 contributes to pepper resistance against P. capsici infection.

resultsIn this study, silencing CaSBP12 significantly increased the expression of defense-related genes (CaBPR1, CaSAR8.2, CaDEF1, CaPO1) in CaSBP12-silenced plants compared to controls after P. capsici inoculation. Even under normal conditions, these genes exhibited higher expression levels in CaSBP12-silenced plants relative to controls. Conversely, these genes were downregulated in CaSBP12-overexpressing pepper plants under stress-free conditions. Therefore, we hypothesized that CaSBP12 mediates the P. capsici defense response through these genes. Further research involved salicylic acid (SA) and jasmonic acid (JA) signaling pathway mutants (sid2, coi1-21, coi1-22) and the NahG gene (salicylate hydroxylase, inhibiting SA accumulation in plants). Without treatment, SA pathway genes AtNPR1, AtTGA6, AtPR1, and AtSARD1 were significantly higher in CaSBP12-overexpressing Arabidopsis thaliana lines than in wild-type, while AtNPR3, AtTGA5, AtPAD4, AtNPR4, and AtNDR1 were lower. In the sid2 mutant, CaSBP12 promoted the expression of SA pathway genes except for AtPR1, which was suppressed. In coi1-21 and coi1-22 mutants, CaSBP12 promoted AtPR1 expression and suppressed the JA pathway gene AtPDF1.2. In NahG and CaSBP12 co-expression lines, SA pathway genes were higher compared to NahG-overexpressing lines, while AtPR1, AtNDR1, AtSARD1, and AtCBP60g levels were lower.

conclusionsCaSBP12 may participate in plant defense responses by regulating the expression of defense-related genes. It may inhibit upstream SA signaling genes NDR1, PAD4, and EDS5 while promoting NPR1 expression and inhibiting NPR3 and NPR4, thereby regulating PR gene expression to participate in plant defense responses. These findings lay the foundation for further elucidating the molecular mechanisms of CaSBP12 in pant defense response against P. capsici infection.

Indexed as

CapsicumDisease ResistancePhytophthoraPlant DiseasesPlant ProteinsSalicylic AcidGene Expression Regulation, PlantOxylipinsSignal TransductionOxylipinsPlant ProteinsSalicylic AcidCaSBP12Defense-related genesPepperPhytophthora capsiciSA signaling pathway

Identifiers

PMID41331556
PMCPMC12777433

What OpenQuestion 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 OpenQuestion graph.