{"title":"Impact of Lepidopteran Oral Secretions on the Transcriptome of <i>Arabidopsis thaliana</i>.","authors":"Angel Fernandez Martin, Philippe Reymond","doi":"10.1002/pld3.70085","DOIUrl":null,"url":null,"abstract":"<p><p>Plants respond to attack by chewing insects through the recognition of herbivore-associated molecular patterns (HAMPs) that are present in oral secretions (OS) and released at the wound site, leading to appropriate deployment of plant immune responses. Because insect feeding is accompanied by severe wounding of the leaf tissue, the specific contribution of HAMPs to defense is not well characterized. Also, OS contain effectors that interfere with the activation of defenses, but the underlying downregulated genes are poorly studied. Here, we analyzed the transcriptome of <i>Arabidopsis thaliana</i> leaves in response to wounding alone or to wounding and application of OS from <i>Spodoptera littoralis</i> or <i>Pieris brassicae</i>. For both insects, OS amplified wound-induced responses and specifically promoted the activation of stress and hormonal pathways, as well as pathogen-related responses. In contrast, OS inhibited the expression of genes involved in the regulation and biosynthesis of aliphatic glucosinolates (GS), and cell wall strengthening. In addition, OS-mediated suppression of wound-induced <i>ERF114</i> and wound healing-related genes uncovered a novel strategy to impair defenses. In support of these findings, we observed an increased performance of <i>S. littoralis</i> and <i>P. brassicae</i> larvae feeding on OS-treated Arabidopsis plants. Altogether, we highlight a major contribution of OS components to plant response to herbivory and unveil the potential role of conserved OS-derived effector(s) in inhibiting defenses.</p>","PeriodicalId":20230,"journal":{"name":"Plant Direct","volume":"9 6","pages":"e70085"},"PeriodicalIF":2.3000,"publicationDate":"2025-06-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12178948/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Direct","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1002/pld3.70085","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/6/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Plants respond to attack by chewing insects through the recognition of herbivore-associated molecular patterns (HAMPs) that are present in oral secretions (OS) and released at the wound site, leading to appropriate deployment of plant immune responses. Because insect feeding is accompanied by severe wounding of the leaf tissue, the specific contribution of HAMPs to defense is not well characterized. Also, OS contain effectors that interfere with the activation of defenses, but the underlying downregulated genes are poorly studied. Here, we analyzed the transcriptome of Arabidopsis thaliana leaves in response to wounding alone or to wounding and application of OS from Spodoptera littoralis or Pieris brassicae. For both insects, OS amplified wound-induced responses and specifically promoted the activation of stress and hormonal pathways, as well as pathogen-related responses. In contrast, OS inhibited the expression of genes involved in the regulation and biosynthesis of aliphatic glucosinolates (GS), and cell wall strengthening. In addition, OS-mediated suppression of wound-induced ERF114 and wound healing-related genes uncovered a novel strategy to impair defenses. In support of these findings, we observed an increased performance of S. littoralis and P. brassicae larvae feeding on OS-treated Arabidopsis plants. Altogether, we highlight a major contribution of OS components to plant response to herbivory and unveil the potential role of conserved OS-derived effector(s) in inhibiting defenses.
期刊介绍:
Plant Direct is a monthly, sound science journal for the plant sciences that gives prompt and equal consideration to papers reporting work dealing with a variety of subjects. Topics include but are not limited to genetics, biochemistry, development, cell biology, biotic stress, abiotic stress, genomics, phenomics, bioinformatics, physiology, molecular biology, and evolution. A collaborative journal launched by the American Society of Plant Biologists, the Society for Experimental Biology and Wiley, Plant Direct publishes papers submitted directly to the journal as well as those referred from a select group of the societies’ journals.