肽聚糖识别蛋白SA参与熊蜂Imd通路免疫应答的机制
批准号:
32102606
项目类别:
青年科学基金项目(C类)
资助金额:
30.0 万元
负责人:
刘彦杰
依托单位:
学科分类:
养蜂学
结题年份:
2024
批准年份:
2021
项目状态:
已结题
项目参与者:
刘彦杰
中文摘要
熊蜂是一类重要的膜翅目传粉昆虫,而病原微生物侵害是其种群数量下降的重要原因。其肽聚糖识别蛋白(PGRPs)介导的Imd和Toll通路免疫应答在清除病原微生物侵染过程中起着十分重要的作用。熊蜂PGRP-SA以高亲和力结合Dap-type肽聚糖介导Imd通路免疫应答,其不同于双翅目果蝇PGRP-SA识别Lys-type肽聚糖介导Toll通路免疫应答。为了揭示熊蜂PGRP-SA识别Dap-type肽聚糖介导Imd通路免疫应答的机制,本项目拟鉴定PGRP-SA-Dap-type肽聚糖复合物的互作受体,验证互作受体参与PGRP-SA介导Imd通路免疫应答的功能。并解析PGRP-SA-Dap-type肽聚糖与互作受体的三维结构,阐明三者的互作结构基础。研究结果将阐明熊蜂PGRP-SA介导Imd通路免疫应答的互作受体及其与PGRP-SA的互作机制,对进一步研究熊蜂的特殊免疫机制及病害防治均有重要意义。
英文摘要
Bumblebee is a type of important Hymenoptera pollinators. However, the colonies of bumblebees have declined dramatically in recent years, and the invasion of pathogens is one of the key factors resulting in the decline of bumblebee colonies. The immune responses of Imd and Toll signaling pathways mediated by peptidoglycan recognition proteins (PGRPs) in bumblebee play an important role in the clearance of pathogen infections. Bumblebee PGRP-SA mediates the immune response of Imd signaling pathway by binding with high affinity to Dap-type peptidoglycan, which differs from the Diptera drosophila PGRP-SA recognizing Lys-type peptidoglycan and participating in the immune response of Toll signaling pathway. To explain the mechanism of bumblebee PGRP-SA recognizing Dap-type peptidoglycan and activating immune response of Imd signaling pathway. This project aims to identify the interaction receptor of PGRP-SA-Dap-type peptidoglycan complex and verify its function in the immune response of Imd pathway mediated by PGRP-SA. The three-dimensional structure of PGRP-SA-Dap-type peptidoglycan and its receptor will be determined to elucidate the structural basis of interaction between PGRP-SA and its interaction receptor. The results will illustrate the interaction receptor of bumblebee PGRP-SA involved in the immune response of Imd signaling pathway and the interaction mechanism between PGRP-SA and its receptor, which is of great significance for further study of the bumblebee's special innate immune mechanism and disease control.
肽聚糖识别蛋白SA(PGRP-SA)是昆虫先天免疫中至关重要的模式识别受体。熊蜂作为一类重要的传粉昆虫,其PGRP-SA能够以高亲和力结合Dap型肽聚糖,进而参与Imd通路免疫应答过程。然而,与双翅目果蝇的PGRP-SA识别Lys型肽聚糖并参与Toll通路免疫应答的机制有所不同。截至目前,熊蜂 PGRP-SA识别Dap型肽聚糖并参与胞内Imd通路免疫应答的具体机制仍不明确。.本研究从以下三个方面展开探究:一是Dap型细菌感染后,PGRP-SA在熊蜂中肠及脂肪体中的免疫应答反应;二是肠道内其他基因表达情况;三是微生物的变化趋势。同时,本研究还对PGRP-SA受体进行了筛选。.研究结果显示,枯草芽孢杆菌(B.subtilis)与大肠杆菌(E.coli)的感染,致使熊蜂中肠的 PGRP-SA、PGRP-LC、Relish及Dorsal基因呈现下调表达,而在脂肪体中,PGRP-SA、PGRP-LC、relish基因则显著上调表达。此外,脂肪体中的抗菌肽Defensin、Hymenoptaecin与Abaecin基因均表现出显著的上调表达趋势,在中肠中仅Defensin、Hymenoptaecin呈现显著上调表达。.中肠转录组与16SrRNA测序结果表明,中肠上调基因主要富集在蛋白合成、能量代谢以及嘌呤代谢相关途径。而且,中肠条件致病菌Alphaproteobacteria的丰度变化,导致了Fructobacillus 菌群的产生。.综上所述,本研究结果表明PGRP-SA介导的免疫应答反应主要在脂肪体发生,通过PGRP-SA/PGRP-LC诱导Imd通路活化,从而诱发抗菌肽Abaecin的表达与释放。抗菌肽Defensin、Hymenoptaecin的合成与释放并不依赖于PGRPs介导的Toll或Imd通路,而是独立发挥抗菌作用或对肠道菌群进行调节。
国内基金
海外基金