Evidence map›Paper›PMID 42907739›Full record

ArticleBMC plant biology2026

Integrated transcriptomic and metabolomic analysis reveals differential molecular mechanisms underlying resistance of native and invasive Phytolacca americana against Spodoptera litura herbivory.

Feiran Jia, Huiyi Lu, Baoya He, Yupeng Geng, Yi Wang, Danfeng Liu, Bo Li

Abstract read
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Article in BMC plant biology, 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Feiran JiaState Key Laboratory of Vegetation Structure, Function and Construction (VegLab), Ministry of Education Key Laboratory for Transboundary Ecosecurity of Southwest China, Yunnan Key Laboratory of Plant Reproductive Adaptation and Evolutionary Ecology, and Institute of Biodiversity, School of Ecology and Environmental Science, Yunnan University, Kunming, China.
Huiyi LuState Key Laboratory of Vegetation Structure, Function and Construction (VegLab), Ministry of Education Key Laboratory for Transboundary Ecosecurity of Southwest China, Yunnan Key Laboratory of Plant Reproductive Adaptation and Evolutionary Ecology, and Institute of Biodiversity, School of Ecology and Environmental Science, Yunnan University, Kunming, China.
Baoya HeState Key Laboratory of Vegetation Structure, Function and Construction (VegLab), Ministry of Education Key Laboratory for Transboundary Ecosecurity of Southwest China, Yunnan Key Laboratory of Plant Reproductive Adaptation and Evolutionary Ecology, and Institute of Biodiversity, School of Ecology and Environmental Science, Yunnan University, Kunming, China.
Yupeng GengState Key Laboratory of Vegetation Structure, Function and Construction (VegLab), Ministry of Education Key Laboratory for Transboundary Ecosecurity of Southwest China, Yunnan Key Laboratory of Plant Reproductive Adaptation and Evolutionary Ecology, and Institute of Biodiversity, School of Ecology and Environmental Science, Yunnan University, Kunming, China.
Yi WangState Key Laboratory of Vegetation Structure, Function and Construction (VegLab), Ministry of Education Key Laboratory for Transboundary Ecosecurity of Southwest China, Yunnan Key Laboratory of Plant Reproductive Adaptation and Evolutionary Ecology, and Institute of Biodiversity, School of Ecology and Environmental Science, Yunnan University, Kunming, China.
Danfeng LiuState Key Laboratory of Vegetation Structure, Function and Construction (VegLab), Ministry of Education Key Laboratory for Transboundary Ecosecurity of Southwest China, Yunnan Key Laboratory of Plant Reproductive Adaptation and Evolutionary Ecology, and Institute of Biodiversity, School of Ecology and Environmental Science, Yunnan University, Kunming, China. dfl@ynu.edu.cn.ORCID https://orcid.org/0000-0002-4630-091X
Bo LiState Key Laboratory of Vegetation Structure, Function and Construction (VegLab), Ministry of Education Key Laboratory for Transboundary Ecosecurity of Southwest China, Yunnan Key Laboratory of Plant Reproductive Adaptation and Evolutionary Ecology, and Institute of Biodiversity, School of Ecology and Environmental Science, Yunnan University, Kunming, China. bool@ynu.edu.cn.

Funding

National Key Research and Development Program of China 2022YFF130240200National Natural Science Foundation of China 32460337Yunnan Revitalization Talent Support Program C6213001257
6 · The paper itself

Abstract

backgroundIn response to herbivory from insects, plants have evolved complex defense strategies. Alien plants often escape control by specialist insects in their introduced range. This release from herbivory pressure may lead to a reallocation of the defensive strategies of alien plants, thereby promoting their invasiveness. However, the molecular mechanisms underlying this resource reallocation process remain unclear. In the present study, we used Phytolacca americana as a model species, and combined transcriptomic and metabolomic analyses to investigate the molecular basis of its invasion success under the herbivory by Spodoptera litura.

resultsHerbivore assays with S. litura revealed that constitutive resistance was comparable between native and invasive P. americana, while induced resistance was significantly lower in invasive P. americana. In the native population, differentially expressed genes and differential abundance metabolites upon S. litura herbivory were mainly enriched in α‑linolenic acid metabolism, the primary pathway for jasmonic acid (JA) formation, whereas in the invasive population, they were predominantly enriched in biosynthesis of amino acids. Notably, the invasive population maintains the synthesis of certain defense metabolites like isoquercitrin, suggesting a defense strategy reconfiguration rather than a complete loss.

conclusionsCollectively, these findings suggest that invasive P. americana may employ a strategic resource reallocation from induced defense to growth metabolism, while JA-mediated induced defense was activated in native P. americana. Our results provide support for the Shifting Defense Hypothesis and advance the mechanisms of plant invasion adaptation.

Indexed as

HerbivoryPhytolacca americanaPlant Defense Against HerbivorySpodopteraTranscriptomeAnimalsCyclopentanesGene Expression ProfilingIntroduced SpeciesMetabolomeMetabolomicsOxylipinsCyclopentanesjasmonic acidOxylipinsHerbivory resistanceNative and invasive Phytolacca americanaTranscriptome-metabolome integration

Identifiers

PMID42907739
PMCPMC13685297

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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.