Evidence map›Paper›PMID 41162188›Full record

ArticleMolecular plant pathology2025

A Secretory Protein Laccase lac8 From Pathogenic Fungi Activates Plant Protein 14-3-3 and Leucine-Rich Repeat Receptor-Like Protein LRR-RLP1 to Trigger Mango Immunity.

Mengting Zhang, Jinji Pu, Chen Lei, Min Zhu, Aiping Gao, Yeyuan Chen, He Zhang

Abstract read
In one paragraph

Article in Molecular plant pathology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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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

7 authors.

Mengting ZhangNational Key Laboratory for Tropical Crop Breeding, Key Laboratory of Integrated Pest Management on Tropical Crops, Ministry of Agriculture and Rural Affairs, Chinese Academy of Tropical Agricultural Sciences Environment and Plant Protection Institute, Haikou, China.
Jinji PuNational Key Laboratory for Tropical Crop Breeding, Key Laboratory of Integrated Pest Management on Tropical Crops, Ministry of Agriculture and Rural Affairs, Chinese Academy of Tropical Agricultural Sciences Environment and Plant Protection Institute, Haikou, China.
Chen LeiNational Key Laboratory for Tropical Crop Breeding, Key Laboratory of Integrated Pest Management on Tropical Crops, Ministry of Agriculture and Rural Affairs, Chinese Academy of Tropical Agricultural Sciences Environment and Plant Protection Institute, Haikou, China.
Min ZhuLaboratory of Crop Gene Resources and Germplasm Enhancement in Southern China, Ministry of Agriculture and Rural Affairs, Chinese Academy of Tropical Agricultural Sciences Tropical Crops Genetic Resources Institute, Haikou, China.
Aiping GaoNational Key Laboratory for Tropical Crop Breeding, Key Laboratory of Integrated Pest Management on Tropical Crops, Ministry of Agriculture and Rural Affairs, Chinese Academy of Tropical Agricultural Sciences Environment and Plant Protection Institute, Haikou, China.
Yeyuan ChenLaboratory of Crop Gene Resources and Germplasm Enhancement in Southern China, Ministry of Agriculture and Rural Affairs, Chinese Academy of Tropical Agricultural Sciences Tropical Crops Genetic Resources Institute, Haikou, China.
He ZhangNational Key Laboratory for Tropical Crop Breeding, Key Laboratory of Integrated Pest Management on Tropical Crops, Ministry of Agriculture and Rural Affairs, Chinese Academy of Tropical Agricultural Sciences Environment and Plant Protection Institute, Haikou, China.ORCID 0000-0002-2699-7094

Funding

National Natural Science Foundation of China 32460398the Central Public-Interest Scientific Institution Basal Research Fund for Chinese Academy of Tropical Agricultural Sciences 1630042022009the China Agriculture Research System of MOF and MARA CARS-31the National Key R&D Program of China 2024YFD1400600the Project of National Key Laboratory for Tropical Crop Breeding NKLTCBCXTD10
6 · The paper itself

Abstract

Plants cope with the biotic stress caused by pathogen infection through complex resistance mechanisms. Here, we identified a secreted laccase Cglac8 from Colletotrichum gloeosporioides and confirmed its involvement in C. gloeosporioides infection of mango (Mangifera indica) plants, as well as its ability to activate the host's innate immune mechanism. Cglac8 interacted with MiLRR-RLP1 and Mi14-3-3-D1 as demonstrated by yeast two-hybrid, bimolecular fluorescence complementation and pull-down assays. The interacting proteins MiLRR-RLP1 and Mi14-3-3-D1 positively regulate mango resistance to C. gloeosporioides by promoting the reactive oxygen species burst and biosynthesis of phytohormones. When Cglac8, MiLRR-RLP1 and Mi14-3-3-D1 proteins were overexpressed together in mango, the resistance of mango to C. gloeosporioides was significantly enhanced. Our findings reveal a new defence mechanism of host plants against C. gloeosporioides, providing a theoretical basis for disease-resistant molecular breeding. The dual role of secretory laccase Cglac8 may reflect a balancing mechanism in host-pathogen co-evolution.

Indexed as

ColletotrichumFungal ProteinsLaccaseMangiferaPlant ImmunityPlant ProteinsDisease ResistanceGene Expression Regulation, PlantPlant DiseasesReactive Oxygen SpeciesFungal ProteinsLaccasePlant ProteinsReactive Oxygen Species14‐3‐3 proteinColletotrichum gloeosporioideslaccaseleucine‐rich repeat receptor‐like proteinmangoplant immunity

Identifiers

PMID41162188
PMCPMC12571544

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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.