Evidence map›Paper›PMID 42427101›Full record

ArticleThe New phytologist2026

The salivary protein NlG8 from Nilaparvata lugens induces both direct and indirect resistance in host rice plants.

Haoli Gao, Xiaowei Yuan, Dong Teng, Ruifang Chen, Jiawen Du, Yongjun Zhang, Zewen Liu

Abstract read
In one paragraph

Article in The New phytologist, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

7 authors.

Haoli GaoState Key Laboratory of Agricultural and Forestry Biosecurity, Nanjing Agricultural University, Weigang 1, Nanjing, 210095, China.ORCID https://orcid.org/0000-0001-9162-1694
Xiaowei YuanState Key Laboratory of Agricultural and Forestry Biosecurity, Nanjing Agricultural University, Weigang 1, Nanjing, 210095, China.
Dong TengState Key Laboratory of Agricultural and Forestry Biosecurity, Nanjing Agricultural University, Weigang 1, Nanjing, 210095, China.
Ruifang ChenState Key Laboratory of Agricultural and Forestry Biosecurity, Nanjing Agricultural University, Weigang 1, Nanjing, 210095, China.
Jiawen DuState Key Laboratory of Agricultural and Forestry Biosecurity, Nanjing Agricultural University, Weigang 1, Nanjing, 210095, China.
Yongjun ZhangState Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing, 100193, China.ORCID https://orcid.org/0000-0003-4276-9072
Zewen LiuState Key Laboratory of Agricultural and Forestry Biosecurity, Nanjing Agricultural University, Weigang 1, Nanjing, 210095, China.ORCID https://orcid.org/0000-0003-1084-9449

Funding

China Postdoctoral Science Foundation 2023M741751Jiangsu Funding Program for Excellent Post-doctoral Talent 2024ZB699National Key Research and Development Program of China 2024YFD1400900National Natural Science Foundation of China 32502472National Postdoctoral Program for Innovative Talents BX20240167Natural Science Foundation of Jiangsu Province BK20241550
6 · The paper itself

Abstract

During feeding, piercing-sucking herbivores inject salivary proteins into the plant, but their roles in modulating direct and indirect plant defenses remain poorly understood. Utilizing an integrated approach that combines transcriptomics, immunoassays, genetic transformation, GC-MS analysis, and bioassays, we identified a novel salivary protein that elicits defense responses in rice. Here, we report a salivary protein, NlG8, from the brown planthopper (BPH), a major piercing-sucking pest of rice. NlG8 localizes to the accessory glands of salivary glands and is secreted into rice plants during feeding as a component of the salivary sheath. Knocking down NlG8 impaired BPH performance and reduced induced plant defenses. Conversely, transgenic rice overexpressing NlG8 enhanced direct defense by upregulating phenylalanine pathway genes. Additionally, NlG8 overexpression induced eight volatiles, including (Z)-3-hexen-1-ol, methyl salicylate, and nonanal, which attracted the natural enemy Tytthus chinensis. These findings reveal that the BPH salivary protein NlG8 not only induces direct rice defenses but also promotes indirect defense by enhancing volatile emissions to recruit natural enemies. Our findings provide new insights into tritrophic interactions and their underlying mechanism, offering valuable genetic and chemical resources for the development of pest control strategies.

Indexed as

HemipteraInsect ProteinsOryzaPlant Defense Against HerbivorySalivary Proteins and PeptidesAmino Acid SequenceAnimalsGene Expression Regulation, PlantHerbivoryPlants, Genetically ModifiedSalivary GlandsVolatile Organic CompoundsInsect ProteinsSalivary Proteins and PeptidesVolatile Organic Compoundsbrown planthoppernatural enemyplant defensesalivary proteintritrophic interactions

Identifiers

PMID42427101
PMCPMC13491270

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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.