Evidence map›Paper›PMID 40163540›Full record

ArticlePLoS pathogens2025

Alternaria alternata effector AaAlta1 targets CmWD40 and participates in regulating disease resistance in Chrysanthemum morifolium.

Shuhuan Zhang, Lina Liu, Wenjie Li, Mengru Yin, Qian Hu, Sumei Chen, Fadi Chen, Ye Liu, Zhiyong Guan, Jiafu Jiang

Abstract read
In one paragraph

Article in PLoS pathogens, 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. Article
  2. Targeted Suppression of the Tomato PathogenJournal of fungi (Basel, Switzerland) · 2026
    Article
  3. Research Progress on Diseases and Pests of Chrysanthemum (2015-2025).International journal of molecular sciences · 2025
    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

10 authors.

Shuhuan ZhangState Key Laboratory of Crop Genetics and Germplasm Enhancement and Utilization, Key Laboratory of Landscaping, Ministry of Agriculture and Rural Affairs, Key Laboratory of State Forestry and Grassland Administration on Biology of Ornamental Plants in East China, College of Horticulture, Nanjing Agricultural University, Nanjing, P. R. China.
Lina LiuState Key Laboratory of Crop Genetics and Germplasm Enhancement and Utilization, Key Laboratory of Landscaping, Ministry of Agriculture and Rural Affairs, Key Laboratory of State Forestry and Grassland Administration on Biology of Ornamental Plants in East China, College of Horticulture, Nanjing Agricultural University, Nanjing, P. R. China.
Wenjie LiState Key Laboratory of Crop Genetics and Germplasm Enhancement and Utilization, Key Laboratory of Landscaping, Ministry of Agriculture and Rural Affairs, Key Laboratory of State Forestry and Grassland Administration on Biology of Ornamental Plants in East China, College of Horticulture, Nanjing Agricultural University, Nanjing, P. R. China.
Mengru YinState Key Laboratory of Crop Genetics and Germplasm Enhancement and Utilization, Key Laboratory of Landscaping, Ministry of Agriculture and Rural Affairs, Key Laboratory of State Forestry and Grassland Administration on Biology of Ornamental Plants in East China, College of Horticulture, Nanjing Agricultural University, Nanjing, P. R. China.
Qian HuState Key Laboratory of Crop Genetics and Germplasm Enhancement and Utilization, Key Laboratory of Landscaping, Ministry of Agriculture and Rural Affairs, Key Laboratory of State Forestry and Grassland Administration on Biology of Ornamental Plants in East China, College of Horticulture, Nanjing Agricultural University, Nanjing, P. R. China.
Sumei ChenState Key Laboratory of Crop Genetics and Germplasm Enhancement and Utilization, Key Laboratory of Landscaping, Ministry of Agriculture and Rural Affairs, Key Laboratory of State Forestry and Grassland Administration on Biology of Ornamental Plants in East China, College of Horticulture, Nanjing Agricultural University, Nanjing, P. R. China.
Fadi ChenState Key Laboratory of Crop Genetics and Germplasm Enhancement and Utilization, Key Laboratory of Landscaping, Ministry of Agriculture and Rural Affairs, Key Laboratory of State Forestry and Grassland Administration on Biology of Ornamental Plants in East China, College of Horticulture, Nanjing Agricultural University, Nanjing, P. R. China.
Ye LiuState Key Laboratory of Crop Genetics and Germplasm Enhancement and Utilization, Key Laboratory of Landscaping, Ministry of Agriculture and Rural Affairs, Key Laboratory of State Forestry and Grassland Administration on Biology of Ornamental Plants in East China, College of Horticulture, Nanjing Agricultural University, Nanjing, P. R. China.
Zhiyong GuanState Key Laboratory of Crop Genetics and Germplasm Enhancement and Utilization, Key Laboratory of Landscaping, Ministry of Agriculture and Rural Affairs, Key Laboratory of State Forestry and Grassland Administration on Biology of Ornamental Plants in East China, College of Horticulture, Nanjing Agricultural University, Nanjing, P. R. China.
Jiafu JiangState Key Laboratory of Crop Genetics and Germplasm Enhancement and Utilization, Key Laboratory of Landscaping, Ministry of Agriculture and Rural Affairs, Key Laboratory of State Forestry and Grassland Administration on Biology of Ornamental Plants in East China, College of Horticulture, Nanjing Agricultural University, Nanjing, P. R. China.ORCID 0000-0002-0078-8796

Funding

Fundamental Research Funds for the Central UniversitiesNational Natural Science Foundation of ChinaZhongshan Biological Breeding Laboratory
6 · The paper itself

Abstract

Black spot diseases caused by the necrotrophic fungal pathogen Alternaria alternata adversely affect the growth and yield of many plants worldwide. However, the molecular mechanisms underlying the virulence and pathogenicity of A. alternata remain largely unknown. In this study, we report the identification of a novel effector Alta1, secreted by A. alternata, which not only contributes to its virulence but also triggers the cell death and defense of the host plant. The expression of Alta1 in Chrysanthemum morifolium activated jasmonic acid (JA) signaling, which, in turn, enhanced plant resistance to A. alternata. Moreover, we found that Alta1 targeted the WD40-repeat protein of chrysanthemum (CmWD40) after entering host cells. Notably, the CmWD40 gene showed rhythmic basal expression, and the overexpression of CmWD40 increased the resistance of chrysanthemum leaves against A. alternata, whereas its loss of function led to a decrease in this resistance. The results of the comparative transcriptomics and JA content analyses indicated that CmWD40 is possibly involved in the accumulation and signaling of JA. The transcript levels of the MYC2 gene were significantly upregulated in lines overexpressing the CmWD40 gene compared with that in the wild type. Further, the results of the infection assay revealed that CmWD40 positively modulated Alta1-induced defense response by activating MYC2 transcription. Overall, the results obtained in this study demonstrate that identified effector Alta1, recognized by the circadian rhythm gene CmWD40, triggers JA-induced immune response and enhances disease resistance in chrysanthemum plants.

Indexed as

AlternariaChrysanthemumDisease ResistanceFungal ProteinsPlant DiseasesPlant ProteinsCyclopentanesGene Expression Regulation, PlantOxylipinsCyclopentanesFungal Proteinsjasmonic acidOxylipinsPlant Proteins

Identifiers

PMID40163540
PMCPMC11957361

What OpenQuestion holds

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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 OpenQuestion graph.