BmPGPR-L4 is a negative regulator of the humoral immune response in the silkworm Bombyx mori

IF 1.5 4区 农林科学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Archives of Insect Biochemistry and Physiology Pub Date : 2024-02-26 DOI:10.1002/arch.22093
Weiyi Yang, Yongyi Lin, Yanying He, Qi Li, Weijian Chen, Qingsha Lin, Luc Swevers, Jisheng Liu
{"title":"BmPGPR-L4 is a negative regulator of the humoral immune response in the silkworm Bombyx mori","authors":"Weiyi Yang,&nbsp;Yongyi Lin,&nbsp;Yanying He,&nbsp;Qi Li,&nbsp;Weijian Chen,&nbsp;Qingsha Lin,&nbsp;Luc Swevers,&nbsp;Jisheng Liu","doi":"10.1002/arch.22093","DOIUrl":null,"url":null,"abstract":"<p>Toll, immune deficiency and prophenoloxidase cascade represent vital immune signaling pathways in insects. Peptidoglycan recognition proteins (PGRPs) are innate immune receptors that activate and regulate the immune signaling pathways. Previously, we reported that <i>BmPGPR-L4</i> was induced in the silkworm <i>Bombyx mori</i> larvae by bacteria and peptidoglycan challenges. Here, we focused on the function of <i>BmPGRP-L4</i> in regulating the expression of antimicrobial peptides (AMPs). The hemolymph from <i>BmPGRP-L4</i>-silenced larvae exhibited an enhanced inhibitory effect on the growth of <i>Escherichia coli</i>, either by growth curve or inhibitory zone experiments. Coincidentally, most of the AMP genes were upregulated after RNAi of <i>BmPGRP-L4</i>. Oral administration of heat-inactivated <i>E. coli</i> and <i>Staphylococcus aureus</i> after RNAi of <i>BmPGRP-L4</i> resulted in the increased expression of <i>BmPGRP-L4</i> in different tissues of the silkworm larvae, revealing an auto-regulatory mechanism. By contrast, the expression of most AMP genes was downregulated by oral bacterial administration after RNAi of <i>BmPGRP-L4</i>. The above results demonstrate that <i>BmPGRP-L4</i> recognizes bacterial pathogen-associated molecular patterns and negatively regulates AMP expression to achieve immunological homeostasis. As a negative regulator, <i>BmPGPR-L4</i> is proposed to be involved in the feedback regulation of the immune signaling pathways of the silkworm to prevent excessive activation of the immune response.</p>","PeriodicalId":8281,"journal":{"name":"Archives of Insect Biochemistry and Physiology","volume":"115 2","pages":""},"PeriodicalIF":1.5000,"publicationDate":"2024-02-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Archives of Insect Biochemistry and Physiology","FirstCategoryId":"97","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/arch.22093","RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Toll, immune deficiency and prophenoloxidase cascade represent vital immune signaling pathways in insects. Peptidoglycan recognition proteins (PGRPs) are innate immune receptors that activate and regulate the immune signaling pathways. Previously, we reported that BmPGPR-L4 was induced in the silkworm Bombyx mori larvae by bacteria and peptidoglycan challenges. Here, we focused on the function of BmPGRP-L4 in regulating the expression of antimicrobial peptides (AMPs). The hemolymph from BmPGRP-L4-silenced larvae exhibited an enhanced inhibitory effect on the growth of Escherichia coli, either by growth curve or inhibitory zone experiments. Coincidentally, most of the AMP genes were upregulated after RNAi of BmPGRP-L4. Oral administration of heat-inactivated E. coli and Staphylococcus aureus after RNAi of BmPGRP-L4 resulted in the increased expression of BmPGRP-L4 in different tissues of the silkworm larvae, revealing an auto-regulatory mechanism. By contrast, the expression of most AMP genes was downregulated by oral bacterial administration after RNAi of BmPGRP-L4. The above results demonstrate that BmPGRP-L4 recognizes bacterial pathogen-associated molecular patterns and negatively regulates AMP expression to achieve immunological homeostasis. As a negative regulator, BmPGPR-L4 is proposed to be involved in the feedback regulation of the immune signaling pathways of the silkworm to prevent excessive activation of the immune response.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
BmPGPR-L4是家蚕体液免疫反应的负调控因子
Toll、免疫缺陷和丙醇氧化酶级联是昆虫体内重要的免疫信号通路。肽聚糖识别蛋白(PGRPs)是先天性免疫受体,可激活和调节免疫信号通路。此前,我们曾报道细菌和肽聚糖挑战会诱导家蚕幼虫体内的 BmPGPR-L4。在此,我们重点研究了 BmPGRP-L4 在调节抗菌肽(AMPs)表达方面的功能。通过生长曲线或抑制区实验,BmPGRP-L4沉默幼虫的血淋巴对大肠杆菌的生长有更强的抑制作用。巧合的是,大多数 AMP 基因在 BmPGRP-L4 的 RNAi 作用下上调。在对 BmPGRP-L4 进行 RNAi 后,口服热灭活的大肠杆菌和金黄色葡萄球菌会导致 BmPGRP-L4 在蚕幼虫不同组织中的表达增加,这揭示了一种自动调节机制。相比之下,在 BmPGRP-L4 的 RNAi 作用下,大多数 AMP 基因在口服细菌后表达下调。上述结果表明,BmPGRP-L4能识别细菌病原体相关分子模式,并负向调节AMP的表达,从而实现免疫平衡。作为一种负调控因子,BmPGPR-L4 被认为参与了家蚕免疫信号通路的反馈调控,以防止免疫反应的过度激活。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
4.30
自引率
4.50%
发文量
115
审稿时长
12 months
期刊介绍: Archives of Insect Biochemistry and Physiology is an international journal that publishes articles in English that are of interest to insect biochemists and physiologists. Generally these articles will be in, or related to, one of the following subject areas: Behavior, Bioinformatics, Carbohydrates, Cell Line Development, Cell Signalling, Development, Drug Discovery, Endocrinology, Enzymes, Lipids, Molecular Biology, Neurobiology, Nucleic Acids, Nutrition, Peptides, Pharmacology, Pollinators, Proteins, Toxicology. Archives will publish only original articles. Articles that are confirmatory in nature or deal with analytical methods previously described will not be accepted.
期刊最新文献
Evaluating the Potential Immunostimulatory Effects of Cryptomeria japonica Leaf Essential Oil on Honey Bees (Apis mellifera) Detecting Brown Planthopper, Nilaparvata lugens (Stål) Damage in Rice Using Hyperspectral Remote Sensing Genetic Control of Social Experience-Dependent Changes in Locomotor Activity in Drosophila melanogaster Males Microcystin-Lr-Induced Changes in Growth Performance, Intestinal Microbiota, and Lipid Metabolism of Black Soldier Fly Larvae (Hermetia illucens) Overexpression of Acetylation-Defective Heat Shock Protein 60 Inhibits the Proliferation of Nucleopolyhedrovirus in Bombyx mori
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1