{"title":"黄颡菌模式识别受体βGRP1和βGRP2的结构和功能研究","authors":"ChunLi Luo, SiQi Chen, FeiYan Gou, DaoWei Zhang, Jing Chen","doi":"10.1007/s13355-023-00833-w","DOIUrl":null,"url":null,"abstract":"<div><p>Beta-1,3-glucan recognition protein (βGRP) is an important pattern recognition receptor, which induces an immune response by recognizing and binding the pathogenic bacteria. In this study, we identified two <i>βGRP</i> genes in <i>S. furcifera</i>, <i>βGRP1</i> and <i>βGRP2</i>. Both βGRP1 and βGRP2 proteins have a glycosyl hydrolases family 16 (GH16) domain and a concanavalin A-like lectin/glucanase domain near the C-terminal. Quantitative polymerase chain reaction (qRT-PCR) analysis showed that the transcript levels of <i>βGRP1</i> and <i>βGRP2</i> in the fat body and gut were higher than those in other tissues. Furthermore, both were upregulated in response to challenges with <i>Escherichia coli</i> and <i>Staphylococcus aureus</i>. Recombinant βGRP1 and βGRP2 had a strong affinity for <i>E</i><i>. coli</i> and <i>S. aureus</i> and caused bacteria to agglutinate. However, the results of the CCK-8 and bacteriostatic zone methods showed that recombinant βGRP1 and βGRP2 inhibited <i>S. aureus</i> but did not inhibit the growth of <i>E. coli.</i> Moreover, the silencing of <i>βGRP1</i> or <i>βGRP2</i> using dsRNA significantly downregulated the expression of the Toll pathway gene <i>Dorsal</i> after <i>S. aureus</i> challenge, while it did not affect the Imd pathway gene <i>Relish</i>.</p></div>","PeriodicalId":8551,"journal":{"name":"Applied Entomology and Zoology","volume":"58 4","pages":"303 - 313"},"PeriodicalIF":1.3000,"publicationDate":"2023-07-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Structural and functional studies of pattern recognition receptors βGRP1 and βGRP2 in Sogatella furcifera\",\"authors\":\"ChunLi Luo, SiQi Chen, FeiYan Gou, DaoWei Zhang, Jing Chen\",\"doi\":\"10.1007/s13355-023-00833-w\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Beta-1,3-glucan recognition protein (βGRP) is an important pattern recognition receptor, which induces an immune response by recognizing and binding the pathogenic bacteria. In this study, we identified two <i>βGRP</i> genes in <i>S. furcifera</i>, <i>βGRP1</i> and <i>βGRP2</i>. Both βGRP1 and βGRP2 proteins have a glycosyl hydrolases family 16 (GH16) domain and a concanavalin A-like lectin/glucanase domain near the C-terminal. Quantitative polymerase chain reaction (qRT-PCR) analysis showed that the transcript levels of <i>βGRP1</i> and <i>βGRP2</i> in the fat body and gut were higher than those in other tissues. Furthermore, both were upregulated in response to challenges with <i>Escherichia coli</i> and <i>Staphylococcus aureus</i>. Recombinant βGRP1 and βGRP2 had a strong affinity for <i>E</i><i>. coli</i> and <i>S. aureus</i> and caused bacteria to agglutinate. However, the results of the CCK-8 and bacteriostatic zone methods showed that recombinant βGRP1 and βGRP2 inhibited <i>S. aureus</i> but did not inhibit the growth of <i>E. coli.</i> Moreover, the silencing of <i>βGRP1</i> or <i>βGRP2</i> using dsRNA significantly downregulated the expression of the Toll pathway gene <i>Dorsal</i> after <i>S. aureus</i> challenge, while it did not affect the Imd pathway gene <i>Relish</i>.</p></div>\",\"PeriodicalId\":8551,\"journal\":{\"name\":\"Applied Entomology and Zoology\",\"volume\":\"58 4\",\"pages\":\"303 - 313\"},\"PeriodicalIF\":1.3000,\"publicationDate\":\"2023-07-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Applied Entomology and Zoology\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s13355-023-00833-w\",\"RegionNum\":4,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ENTOMOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Applied Entomology and Zoology","FirstCategoryId":"97","ListUrlMain":"https://link.springer.com/article/10.1007/s13355-023-00833-w","RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENTOMOLOGY","Score":null,"Total":0}
Structural and functional studies of pattern recognition receptors βGRP1 and βGRP2 in Sogatella furcifera
Beta-1,3-glucan recognition protein (βGRP) is an important pattern recognition receptor, which induces an immune response by recognizing and binding the pathogenic bacteria. In this study, we identified two βGRP genes in S. furcifera, βGRP1 and βGRP2. Both βGRP1 and βGRP2 proteins have a glycosyl hydrolases family 16 (GH16) domain and a concanavalin A-like lectin/glucanase domain near the C-terminal. Quantitative polymerase chain reaction (qRT-PCR) analysis showed that the transcript levels of βGRP1 and βGRP2 in the fat body and gut were higher than those in other tissues. Furthermore, both were upregulated in response to challenges with Escherichia coli and Staphylococcus aureus. Recombinant βGRP1 and βGRP2 had a strong affinity for E. coli and S. aureus and caused bacteria to agglutinate. However, the results of the CCK-8 and bacteriostatic zone methods showed that recombinant βGRP1 and βGRP2 inhibited S. aureus but did not inhibit the growth of E. coli. Moreover, the silencing of βGRP1 or βGRP2 using dsRNA significantly downregulated the expression of the Toll pathway gene Dorsal after S. aureus challenge, while it did not affect the Imd pathway gene Relish.
期刊介绍:
Applied Entomology and Zoology publishes articles concerned with applied entomology, applied zoology, agricultural chemicals and pest control in English. Contributions of a basic and fundamental nature may be accepted at the discretion of the Editor. Manuscripts of original research papers, technical notes and reviews are accepted for consideration. No manuscript that has been published elsewhere will be accepted for publication.