血腥素能增强毛虫对 NPV 感染的免疫反应。

IF 2.3 2区 农林科学 Q1 ENTOMOLOGY Journal of insect physiology Pub Date : 2024-05-18 DOI:10.1016/j.jinsphys.2024.104651
Liqiong Yan, Arina Nur Faidah, Lili Sun, Chuanwang Cao
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引用次数: 0

摘要

Hemolin是免疫球蛋白超家族的一员,在昆虫对病原体的免疫反应中起着至关重要的作用。然而,Hemolin对杆状病毒感染的先天性免疫反应在不同昆虫之间存在差异,而Hemolin在Hyphantria cunea(HcHemolin)中的抗病毒作用仍然鲜为人知。我们的研究结果表明,HcHemolin 在所有发育阶段都有表达,在蛹和成虫阶段的表达量更高。此外,HcHemolin 在生殖器官和消化器官中也有表达。HcNPV 感染后,HcHemolin 的表达水平被显著诱导。沉默HcHemolin后,胭脂鱼幼虫对HcNPV的敏感性降低,与对照组相比,中位寿命缩短了40%。沉默组 H. cunea 幼虫的相对生长率(RGR)、相对消耗率效率(RCR)、摄入食物转化效率(ECI)和消化食物转化效率(ECD)显著低于对照组。免疫挑战实验表明,HcNPV和HcHemolin蛋白联合注射后,处理组H. cunea幼虫的中位寿命是对照组的两倍。因此,我们认为 HcHemolin 在调控楔尾蛙的生长、发育和食物利用以及对 HcNPV 的抗病毒免疫反应中起着至关重要的作用。这些发现为开发有针对性的核酸农药和无公害生物防治 HcNPV 增效剂的新策略提供了启示。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Hemolin increases the immune response of a caterpillar to NPV infection

Hemolin, a member of the immunoglobulin superfamily, plays a crucial role in the immune responses of insects against pathogens. However, the innate immune response of Hemolin to baculovirus infection varies among different insects, and the antiviral effects of Hemolin in Hyphantria cunea (HcHemolin) remain poorly understood. Our results showed that HcHemolin was expressed throughout all developmental stages, with higher expressions observed during pupal and adult stages of H. cunea. Additionally, HcHemolin was expressed in reproductive and digestive organs. The expression levels of the HcHemolin were induced significantly following H. cunea nucleopolyhedrovirus (HcNPV) infection. The susceptibility of H. cunea larvae to HcNPV decreased upon silencing of HcHemolin, resulting in a 40% reduction in median lifespan compared to the control group. The relative growth rate (RGR), the relative efficiency of consumption rate (RCR), the efficiency of the conversion of ingested food (ECI), and efficiency of the conversion of digested food (ECD) of silenced H. cunea larvae were significantly lower than those of the control group. Immune challenge assays showed that the median lifespan of treated H. cunea larvae was two-fold longer than the control group after HcNPV and HcHemolin protein co-injection. Therefore, we propose that HcHemolin plays a crucial role in regulating the growth, development, and food utilization of H. cunea, as well as in the antiviral immune response against HcNPV. These findings provide implications for the development of targeted nucleic acid pesticides and novel strategies for pollution-free biological control synergists for HcNPV.

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来源期刊
Journal of insect physiology
Journal of insect physiology 生物-昆虫学
CiteScore
4.50
自引率
4.50%
发文量
77
审稿时长
57 days
期刊介绍: All aspects of insect physiology are published in this journal which will also accept papers on the physiology of other arthropods, if the referees consider the work to be of general interest. The coverage includes endocrinology (in relation to moulting, reproduction and metabolism), pheromones, neurobiology (cellular, integrative and developmental), physiological pharmacology, nutrition (food selection, digestion and absorption), homeostasis, excretion, reproduction and behaviour. Papers covering functional genomics and molecular approaches to physiological problems will also be included. Communications on structure and applied entomology can be published if the subject matter has an explicit bearing on the physiology of arthropods. Review articles and novel method papers are also welcomed.
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