新发现的c型凝集素(TcCTL17)在木栗的免疫和发育中的双重功能。

IF 1.6 3区 农林科学 Q2 ENTOMOLOGY
Peng Chen, Huayi Ai, Zhiping Liu, Chengjun Li, Bin Li
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引用次数: 0

摘要

c型凝集素(ctl)是一种多样化的模式识别受体家族,对无脊椎动物的免疫识别和病原体清除至关重要。TcCTL17包含1个碳水化合物识别结构域和3个富含cys的清道夫受体结构域。时空表达分析显示,TcCTL17在20 d的早期蛹、早期成虫和幼虫肠道中高表达。重组TcCTL17在体外表现出与脂多糖和肽聚糖的剂量依赖性结合,Ca2+依赖性结合和细菌的凝集性。在细菌暴露前敲除TcCTL17会降低castaneum幼虫的存活率,增加细菌负荷,同时降低抗菌肽表达和血淋巴酚氧化酶活性。此外,TcCTL17 RNA干扰可能通过影响20E、JH和卵黄原蛋白通路导致发育异常,影响变态和繁殖力。这些发现强调了TcCTL17在免疫和发育中的双重功能,使其成为害虫防治的潜在靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The dual functions of a newly identified C-type lectin (TcCTL17) in the immunity and development of Tribolium castaneum.

C-type lectins (CTLs), a diverse family of pattern recognition receptors, are essential for immune recognition and pathogen clearance in invertebrates. TcCTL17 contains one carbohydrate recognition domain and three scavenger receptor Cys-rich domains. Spatial and temporal expression analysis revealed that TcCTL17 is highly expressed in early pupa, early adult stages, and the larval gut at 20 days. The recombinant TcCTL17 exhibited dose-dependent binding to lipopolysaccharides and peptidoglycans, Ca2+-dependent binding and agglutination of bacteria in vitro. Knocking down TcCTL17 before bacterial exposure reduced survival rates and increased bacterial loads in T. castaneum larvae, accompanied by decreased antimicrobial peptide expression and haemolymph phenoloxidase activity. Additionally, TcCTL17 RNA interference caused developmental abnormalities, affecting metamorphosis and fecundity, possibly by influencing the 20E, JH, and vitellogenin pathways. These findings underscore dual functions of TcCTL17 in immunity and development, making it a potential target for pest management.

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来源期刊
CiteScore
4.00
自引率
0.00%
发文量
160
审稿时长
6-12 weeks
期刊介绍: Established in 1910, the internationally recognised Bulletin of Entomological Research aims to further global knowledge of entomology through the generalisation of research findings rather than providing more entomological exceptions. The Bulletin publishes high quality and original research papers, ''critiques'' and review articles concerning insects or other arthropods of economic importance in agriculture, forestry, stored products, biological control, medicine, animal health and natural resource management. The scope of papers addresses the biology, ecology, behaviour, physiology and systematics of individuals and populations, with a particular emphasis upon the major current and emerging pests of agriculture, horticulture and forestry, and vectors of human and animal diseases. This includes the interactions between species (plants, hosts for parasites, natural enemies and whole communities), novel methodological developments, including molecular biology, in an applied context. The Bulletin does not publish the results of pesticide testing or traditional taxonomic revisions.
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