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蜜蜂寄生螨瓦螨中速激肽和 Natalisin 神经肽系统的配体选择性。

Ligand selectivity in tachykinin and natalisin neuropeptidergic systems of the honey bee parasitic mite Varroa destructor.

机构信息

Department of Entomology, Kansas State University, Manhattan, Kansas 66506, United States.

Key Laboratory of Entomology and Pest Control Engineering, College of Plant Protection, Southwest University, Chongqing 400715, People's Republic of China.

出版信息

Sci Rep. 2016 Jan 28;6:19547. doi: 10.1038/srep19547.

Abstract

The varroa mite, Varroa destructor, is a devastating ectoparasite of the honey bees Apis mellifera and A. cerana. Control of these mites in beehives is a challenge in part due to the lack of toxic agents that are specific to mites and not to the host honey bee. In searching for a specific toxic target of varroa mites, we investigated two closely related neuropeptidergic systems, tachykinin-related peptide (TRP) and natalisin (NTL), and their respective receptors. Honey bees lack both NTL and the NTL receptor in their genome sequences, providing the rationale for investigating these receptors to understand their specificities to various ligands. We characterized the receptors for NTL and TRP of V. destructor (VdNTL-R and VdTRP-R, respectively) and for TRP of A. mellifera (AmTRP-R) in a heterologous reporter assay system to determine the activities of various ligands including TRP/NTL peptides and peptidomimetics. Although we found that AmTRP-R is highly promiscuous, activated by various ligands including two VdNTL peptides when a total of 36 ligands were tested, we serendipitously found that peptides carrying the C-terminal motif -FWxxRamide are highly specific to VdTRP-R. This motif can serve as a seed sequence for designing a VdTRP-R-specific agonist.

摘要

瓦螨(Varroa destructor)是蜜蜂(Apis mellifera 和 A. cerana)的一种破坏性外寄生虫。在蜂箱中控制这些螨虫在一定程度上是一个挑战,部分原因是缺乏专门针对螨虫而不是宿主蜜蜂的有毒物质。在寻找瓦螨的特定毒性靶标时,我们研究了两种密切相关的神经肽系统,速激肽相关肽(TRP)和 Natalisin(NTL)及其各自的受体。蜜蜂基因组序列中缺乏 NTL 和 NTL 受体,这为研究这些受体提供了理由,以了解它们对各种配体的特异性。我们在异源报告基因检测系统中鉴定了 V. destructor 的 NTL 和 TRP 受体(分别为 VdNTL-R 和 VdTRP-R)以及 A. mellifera 的 TRP 受体(AmTRP-R),以确定各种配体的活性,包括 TRP/NTL 肽和肽模拟物。虽然我们发现 AmTRP-R 高度混杂,可被包括两种 VdNTL 肽在内的各种配体激活,当总共测试了 36 种配体时,我们偶然发现携带 C 末端基序-FWxxRamide 的肽对 VdTRP-R 具有高度特异性。这个基序可以作为设计 VdTRP-R 特异性激动剂的种子序列。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3a8/4730192/ea85297fb52d/srep19547-f1.jpg

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