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小菜蛾肠道反流物中的HSC70-3:宿主植物适应性的候选效应因子

HSC70-3 in the Gut Regurgitant of Diamondback Moth, : A Candidate Effector for Host Plant Adaptation.

作者信息

Qiao Qingxuan, Zheng Chanqin, Feng Huiting, Huang Shihua, Wang Bing, Zaheer Uroosa, He Weiyi

机构信息

State Key Laboratory of Agricultural and Forestry Biosecurity, Institute of Applied Ecology, Fujian Agriculture and Forestry University, Fuzhou 350002, China.

International Joint Research Laboratory of Ecological Pest Control, Ministry of Education and Ministerial and Provincial Joint Innovation Centre for Safety Production of Cross-Strait Crops, Fujian Agriculture and Forestry University, Fuzhou 350002, China.

出版信息

Insects. 2025 May 2;16(5):489. doi: 10.3390/insects16050489.

DOI:10.3390/insects16050489
PMID:40429202
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12112308/
Abstract

The co-evolution between plants and herbivorous insects has led to a continuous arms race on defense and anti-defense mechanisms. In this process, insect-derived effectors are crucial for suppressing plant defense. Despite considerable progress in plant-insect interaction studies, the functional role of heat shock cognate protein 70 (HSC70) as an effector in herbivorous insects remains poorly characterized. This study provides evidence that HSC70-3 functions as an effector in interactions between the cruciferous specialist diamondback moth () and its host plant radish ( 'Nanpan Prefecture'). Using immunofluorescence labeling and in situ Western blot (WB), we demonstrated that HSC70-3 is secreted into plant wound sites through larval gut regurgitant during feeding. Short-term host transfer experiments revealed tissue-specific expression changes, indicating a dynamic response to plant-derived challenges. These findings suggest is differentially regulated at transcriptional and translational levels to facilitate insect adaptation to host plant shifts. Knockout of using CRISPR/Cas9 technology significantly impaired larval growth, prolonged development duration, and reduced pupal weight on host plants, indicating its involvement in host adaptation. However, knockout mutants exhibited no significant developmental defects when reared on an artificial diet, suggesting that primarily functions in modulating plant-induced defense responses rather than directly affecting insect physiology. Collectively, these findings provide evidence for the functional roles of HSC70-3 in and plant interactions, laying a foundation for further investigations into insect effectors and their mechanisms in modulating plant defense responses.

摘要

植物与食草昆虫之间的共同进化导致了防御与反防御机制的持续军备竞赛。在此过程中,昆虫衍生的效应子对于抑制植物防御至关重要。尽管植物-昆虫相互作用研究取得了显著进展,但热休克同源蛋白70(HSC70)作为食草昆虫中的效应子,其功能作用仍鲜为人知。本研究提供了证据,表明HSC70-3在十字花科专食性小菜蛾()与其寄主植物萝卜(‘黔南州’)的相互作用中作为效应子发挥作用。通过免疫荧光标记和原位蛋白质免疫印迹(WB),我们证明了在取食期间,HSC70-3通过幼虫肠道反流物分泌到植物伤口部位。短期寄主转移实验揭示了组织特异性的表达变化,表明对植物衍生挑战的动态响应。这些发现表明在转录和翻译水平上受到差异调节,以促进昆虫适应寄主植物的转变。使用CRISPR/Cas9技术敲除会显著损害幼虫生长,延长发育时间,并降低寄主植物上的蛹重,表明其参与寄主适应。然而,在人工饲料上饲养时,敲除突变体没有表现出明显的发育缺陷,这表明主要在调节植物诱导的防御反应中发挥作用,而不是直接影响昆虫生理。总的来说,这些发现为HSC70-3在与植物相互作用中的功能作用提供了证据,为进一步研究昆虫效应子及其调节植物防御反应的机制奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c89/12112308/8b6283b99248/insects-16-00489-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c89/12112308/7ac2f6907b33/insects-16-00489-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c89/12112308/b69dc0fc8a2a/insects-16-00489-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c89/12112308/789040972cf5/insects-16-00489-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c89/12112308/527c0ad756d5/insects-16-00489-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c89/12112308/c84b50936050/insects-16-00489-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c89/12112308/32e897db3c12/insects-16-00489-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c89/12112308/8b6283b99248/insects-16-00489-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c89/12112308/7ac2f6907b33/insects-16-00489-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c89/12112308/b69dc0fc8a2a/insects-16-00489-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c89/12112308/789040972cf5/insects-16-00489-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c89/12112308/527c0ad756d5/insects-16-00489-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c89/12112308/c84b50936050/insects-16-00489-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c89/12112308/32e897db3c12/insects-16-00489-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c89/12112308/8b6283b99248/insects-16-00489-g007.jpg

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本文引用的文献

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Bacteria Derived from Diamondback Moth, (L.) (Lepidoptera: Plutellidae), Gut Regurgitant Negatively Regulate Glucose Oxidase-Mediated Anti-Defense Against Host Plant.小菜蛾(鳞翅目:菜蛾科)肠道反流物中的细菌对葡萄糖氧化酶介导的宿主植物抗防御起负调控作用。
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