病原体反应基因(REPAT)SfREPAT38 通过介导 Toll 信号通路参与鞘翅目幼虫的免疫反应。

IF 2.3 2区 农林科学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Yuxue Wang, Natasha Isabel Tanatsiwa Mbiza, Ting Liu, Yi Wang, Yi Zhang, Xincheng Luo, Longyan Chu, Jianping Li, Yazhen Yang, Xiangping Wang, Jianmin Zhang, Yonghao Yu
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引用次数: 0

摘要

REPAT(对病原体的反应)是一个免疫相关基因家族,在昆虫对病原体的免疫反应中发挥着重要作用。尽管目前已在鳞翅目蛙科(Spodoptera frugiperda)中发现了 9 个 REPAT 基因,但它们在对病原体的免疫应答中的功能和机制仍不清楚。因此,研究人员对鞘翅目蛙科昆虫的病原体应答基因(REPAT)SfREPAT38进行了特征描述和功能分析。结果表明,SfREPAT38含有一个信号肽和一个转录激活因子MBF2(多蛋白桥接因子2)结构域。定量实时聚合酶链反应分析表明,SfREPAT38在六龄幼虫(L6)中高表达,在L6的中肠中表达量最高。我们发现,SfREPAT38的表达可被四种微生物病原体(苏云金芽孢杆菌、甲线虫、核多角体病和大肠杆菌)激活,但大肠杆菌感染后12 h除外。此外,注射或喂食 SfREPAT38 dsRNA 后 24、48 和 72 h,SfREPAT38 的表达水平显著下降。喂食 SfREPAT38 dsRNA 会明显降低俭毛蛛的增重,连续喂食会导致俭毛蛛幼虫从第四天开始死亡。此外,注射 SfREPAT38 dsRNA 会导致第五天的增重显著下降。沉默SfREPAT38基因可下调Toll通路免疫基因的表达水平,包括SPZ、Myd88、DIF、Cactus、Pell和Toll18W。经 SfREPAT38 dsRNA 处理后,褶鳃蝇对苏云金杆菌感染变得极为敏感,存活率急剧上升,第八天死亡率达 100%。从第 2 天开始,S. frugiperda 幼虫的体重也明显低于对照组。此外,参与 Toll 信号通路的基因和一些抗菌肽相关基因在处理后出现下调。这些结果表明,SfREPAT38 通过介导 Toll 信号通路参与了节肢动物幼虫的免疫反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

SfREPAT38, a pathogen response gene (REPAT), is involved in immune response of Spodoptera frugiperda larvae through mediating Toll signalling pathway

SfREPAT38, a pathogen response gene (REPAT), is involved in immune response of Spodoptera frugiperda larvae through mediating Toll signalling pathway

SfREPAT38, a pathogen response gene (REPAT), is involved in immune response of Spodoptera frugiperda larvae through mediating Toll signalling pathway

REPAT (response to pathogen) is an immune-associated gene family that plays important roles in insect immune response to pathogens. Although nine REPAT genes have been identified in Spodoptera frugiperda (Lepidoptera: Noctuidae) currently, their functions and mechanisms in the immune response to pathogens still remain unclear. Therefore, SfREPAT38, a pathogen response gene (REPAT) of S. frugiperda, was characterised and its function was analysed. The results showed that SfREPAT38 contains a signal peptide and a transcription activator MBF2 (multi-protein bridging factor 2) domain. Quantitative real-time polymerase chain reaction analysis showed that SfREPAT38 was highly expressed in the sixth-instar larvae (L6) and was the highest in expression in the midgut of L6. We found that the expression of SfREPAT38 could be activated by challenge with four microbial pathogens (Bacillus thuringiensis, Metarhizium anisopliae, Spodoptera exigua nuclearpolyhedrosis and Escherichia coli), except 12 h after E. coli infection. Furthermore, the SfREPAT38 expression levels significantly decreased at 24, 48 and 72 h after SfREPAT38 dsRNA injection or feeding. Feeding with SfREPAT38 dsRNA significantly decreased the weight gain of S. frugiperda, and continuous feeding led to the death of S. frugiperda larvae from the fourth day. Moreover, SfREPAT38 dsRNA injection resulted in a significant decrease of weight gain on the fifth day. Silencing SfREPAT38 gene down-regulated the expression levels of immune genes belonging to the Toll pathway, including SPZ, Myd88, DIF, Cactus, Pell and Toll18W. After treatment with SfREPAT38 dsRNA, S. frugiperda became extremely sensitive to the B. thuringiensis infection, and the survival rate dramatically increased, with 100% mortality by the eighth day. The weight of S. frugiperda larvae was also significantly lower than that of the control groups from the second day onwards. In addition, the genes involved in the Toll signalling pathway and a few antibacterial peptide related genes were down-regulated after treatment. These results showed that SfREPAT38 is involved in the immune response of S. frugiperda larvae through mediating Toll signalling pathway.

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来源期刊
Insect Molecular Biology
Insect Molecular Biology 生物-昆虫学
CiteScore
4.80
自引率
3.80%
发文量
68
审稿时长
6-12 weeks
期刊介绍: Insect Molecular Biology has been dedicated to providing researchers with the opportunity to publish high quality original research on topics broadly related to insect molecular biology since 1992. IMB is particularly interested in publishing research in insect genomics/genes and proteomics/proteins. This includes research related to: • insect gene structure • control of gene expression • localisation and function/activity of proteins • interactions of proteins and ligands/substrates • effect of mutations on gene/protein function • evolution of insect genes/genomes, especially where principles relevant to insects in general are established • molecular population genetics where data are used to identify genes (or regions of genomes) involved in specific adaptations • gene mapping using molecular tools • molecular interactions of insects with microorganisms including Wolbachia, symbionts and viruses or other pathogens transmitted by insects Papers can include large data sets e.g.from micro-array or proteomic experiments or analyses of genome sequences done in silico (subject to the data being placed in the context of hypothesis testing).
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