{"title":"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。","authors":"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","doi":"10.1111/imb.12909","DOIUrl":null,"url":null,"abstract":"<p>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 <i>Spodoptera frugiperda</i> (Lepidoptera: Noctuidae) currently, their functions and mechanisms in the immune response to pathogens still remain unclear. Therefore, <i>SfREPAT38</i>, a pathogen response gene (REPAT) of <i>S. frugiperda</i>, was characterised and its function was analysed. The results showed that <i>SfREPAT38</i> contains a signal peptide and a transcription activator MBF2 (multi-protein bridging factor 2) domain. Quantitative real-time polymerase chain reaction analysis showed that <i>SfREPAT38</i> 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 <i>SfREPAT38</i> could be activated by challenge with four microbial pathogens (<i>Bacillus thuringiensis</i>, <i>Metarhizium anisopliae</i>, <i>Spodoptera exigua</i> nuclearpolyhedrosis and <i>Escherichia coli</i>), except 12 h after <i>E. coli</i> infection. Furthermore, the <i>SfREPAT38</i> expression levels significantly decreased at 24, 48 and 72 h after <i>SfREPAT38</i> dsRNA injection or feeding. Feeding with <i>SfREPAT38</i> dsRNA significantly decreased the weight gain of <i>S. frugiperda</i>, and continuous feeding led to the death of <i>S. frugiperda</i> larvae from the fourth day. Moreover, <i>SfREPAT3</i>8 dsRNA injection resulted in a significant decrease of weight gain on the fifth day. Silencing <i>SfREPAT38</i> gene down-regulated the expression levels of immune genes belonging to the Toll pathway, including <i>SPZ</i>, <i>Myd88</i>, <i>DIF</i>, <i>Cactus</i>, <i>Pell</i> and <i>Toll18W.</i> After treatment with <i>SfREPAT3</i>8 dsRNA, <i>S. frugiperda</i> became extremely sensitive to the <i>B. thuringiensis</i> infection, and the survival rate dramatically increased, with 100% mortality by the eighth day. The weight of <i>S. frugiperda</i> 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 <i>SfREPAT38</i> is involved in the immune response of <i>S. frugiperda</i> larvae through mediating Toll signalling pathway.</p>","PeriodicalId":13526,"journal":{"name":"Insect Molecular Biology","volume":"33 4","pages":"417-426"},"PeriodicalIF":2.3000,"publicationDate":"2024-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"SfREPAT38, a pathogen response gene (REPAT), is involved in immune response of Spodoptera frugiperda larvae through mediating Toll signalling pathway\",\"authors\":\"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\",\"doi\":\"10.1111/imb.12909\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>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 <i>Spodoptera frugiperda</i> (Lepidoptera: Noctuidae) currently, their functions and mechanisms in the immune response to pathogens still remain unclear. Therefore, <i>SfREPAT38</i>, a pathogen response gene (REPAT) of <i>S. frugiperda</i>, was characterised and its function was analysed. The results showed that <i>SfREPAT38</i> contains a signal peptide and a transcription activator MBF2 (multi-protein bridging factor 2) domain. Quantitative real-time polymerase chain reaction analysis showed that <i>SfREPAT38</i> 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 <i>SfREPAT38</i> could be activated by challenge with four microbial pathogens (<i>Bacillus thuringiensis</i>, <i>Metarhizium anisopliae</i>, <i>Spodoptera exigua</i> nuclearpolyhedrosis and <i>Escherichia coli</i>), except 12 h after <i>E. coli</i> infection. Furthermore, the <i>SfREPAT38</i> expression levels significantly decreased at 24, 48 and 72 h after <i>SfREPAT38</i> dsRNA injection or feeding. Feeding with <i>SfREPAT38</i> dsRNA significantly decreased the weight gain of <i>S. frugiperda</i>, and continuous feeding led to the death of <i>S. frugiperda</i> larvae from the fourth day. Moreover, <i>SfREPAT3</i>8 dsRNA injection resulted in a significant decrease of weight gain on the fifth day. Silencing <i>SfREPAT38</i> gene down-regulated the expression levels of immune genes belonging to the Toll pathway, including <i>SPZ</i>, <i>Myd88</i>, <i>DIF</i>, <i>Cactus</i>, <i>Pell</i> and <i>Toll18W.</i> After treatment with <i>SfREPAT3</i>8 dsRNA, <i>S. frugiperda</i> became extremely sensitive to the <i>B. thuringiensis</i> infection, and the survival rate dramatically increased, with 100% mortality by the eighth day. The weight of <i>S. frugiperda</i> 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 <i>SfREPAT38</i> is involved in the immune response of <i>S. frugiperda</i> larvae through mediating Toll signalling pathway.</p>\",\"PeriodicalId\":13526,\"journal\":{\"name\":\"Insect Molecular Biology\",\"volume\":\"33 4\",\"pages\":\"417-426\"},\"PeriodicalIF\":2.3000,\"publicationDate\":\"2024-03-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Insect Molecular Biology\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/imb.12909\",\"RegionNum\":2,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Insect Molecular Biology","FirstCategoryId":"97","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/imb.12909","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
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.
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).