Jianjun Feng , Peng Lin , Yilei Wang , Songlin Guo , Ziping Zhang , Lili Yu
{"title":"日本鳗鲡ⅰ型干扰素(IFN)基因的鉴定及体内外表达分析","authors":"Jianjun Feng , Peng Lin , Yilei Wang , Songlin Guo , Ziping Zhang , Lili Yu","doi":"10.1016/j.aggene.2017.07.003","DOIUrl":null,"url":null,"abstract":"<div><p><span>Type I interferon (IFN) is a key cytokine of innate immune response for viral infection in teleost fish. In present study we report the identification of a type I IFN gene (</span><em>Aj</em><span>IFN) from Japanese eel (</span><em>Anguilla japonica</em>) and provide evidence that <em>Aj</em>IFN has been involved in Japanese eel host response against not only the virus but also the bacterial infection. The full-length cDNA of <em>Aj</em>IFN (826<!--> <!-->bp) has an ORF of 531<!--> <!-->bp. The analysis of NCBI CDD showed that the <em>Aj</em><span><span>IFN protein had the typical conserved domains, including IFabd conserved domain, and two conserved cysteine residues potentially forming disulphide bridges. Based on the </span>phylogenetic analysis, </span><em>Aj</em>IFN was classified into type I IFNs families belonging to the subgroup-a of the 2Cys group. <em>In vivo</em>, the <em>Aj</em>IFN expressions in liver and kidney were induced following injection with LPS, the viral mimic poly I:C, and <span><em>Aeromonas hydrophila</em></span> infection. <em>In vitro</em>, the <em>Aj</em>IFN transcripts of Japanese eel liver cells were enhanced by LPS, poly I:C and CpG-DNA stimulation and no change of the expression level was found post PGN treatment. Following <em>A. hydrophila</em> infection, the low concentration of 1<!--> <!-->×<!--> <!-->10<sup>6</sup> <!-->cfu/mL failed to induce the expression of <em>Aj</em>IFN whereas the concentration of 1<!--> <!-->×<!--> <!-->10<sup>7</sup> <!-->cfu/mL and 1<!--> <!-->×<!--> <!-->10<sup>8</sup> <!-->cfu/mL successfully induced the expression of <em>Aj</em>IFN. These results collectively suggested <em>Aj</em>IFN is an inducible gene possibly involved in Japanese eel defense against viral and bacterial infection.</p></div>","PeriodicalId":37751,"journal":{"name":"Agri Gene","volume":"5 ","pages":"Pages 19-26"},"PeriodicalIF":0.0000,"publicationDate":"2017-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.aggene.2017.07.003","citationCount":"5","resultStr":"{\"title\":\"Identification of a type I interferon (IFN) gene from Japanese eel and its expression analysis in vivo and in vitro\",\"authors\":\"Jianjun Feng , Peng Lin , Yilei Wang , Songlin Guo , Ziping Zhang , Lili Yu\",\"doi\":\"10.1016/j.aggene.2017.07.003\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><span>Type I interferon (IFN) is a key cytokine of innate immune response for viral infection in teleost fish. In present study we report the identification of a type I IFN gene (</span><em>Aj</em><span>IFN) from Japanese eel (</span><em>Anguilla japonica</em>) and provide evidence that <em>Aj</em>IFN has been involved in Japanese eel host response against not only the virus but also the bacterial infection. The full-length cDNA of <em>Aj</em>IFN (826<!--> <!-->bp) has an ORF of 531<!--> <!-->bp. The analysis of NCBI CDD showed that the <em>Aj</em><span><span>IFN protein had the typical conserved domains, including IFabd conserved domain, and two conserved cysteine residues potentially forming disulphide bridges. Based on the </span>phylogenetic analysis, </span><em>Aj</em>IFN was classified into type I IFNs families belonging to the subgroup-a of the 2Cys group. <em>In vivo</em>, the <em>Aj</em>IFN expressions in liver and kidney were induced following injection with LPS, the viral mimic poly I:C, and <span><em>Aeromonas hydrophila</em></span> infection. <em>In vitro</em>, the <em>Aj</em>IFN transcripts of Japanese eel liver cells were enhanced by LPS, poly I:C and CpG-DNA stimulation and no change of the expression level was found post PGN treatment. Following <em>A. hydrophila</em> infection, the low concentration of 1<!--> <!-->×<!--> <!-->10<sup>6</sup> <!-->cfu/mL failed to induce the expression of <em>Aj</em>IFN whereas the concentration of 1<!--> <!-->×<!--> <!-->10<sup>7</sup> <!-->cfu/mL and 1<!--> <!-->×<!--> <!-->10<sup>8</sup> <!-->cfu/mL successfully induced the expression of <em>Aj</em>IFN. These results collectively suggested <em>Aj</em>IFN is an inducible gene possibly involved in Japanese eel defense against viral and bacterial infection.</p></div>\",\"PeriodicalId\":37751,\"journal\":{\"name\":\"Agri Gene\",\"volume\":\"5 \",\"pages\":\"Pages 19-26\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2017-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.aggene.2017.07.003\",\"citationCount\":\"5\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Agri Gene\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2352215117300120\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"Agricultural and Biological Sciences\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Agri Gene","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2352215117300120","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Agricultural and Biological Sciences","Score":null,"Total":0}
Identification of a type I interferon (IFN) gene from Japanese eel and its expression analysis in vivo and in vitro
Type I interferon (IFN) is a key cytokine of innate immune response for viral infection in teleost fish. In present study we report the identification of a type I IFN gene (AjIFN) from Japanese eel (Anguilla japonica) and provide evidence that AjIFN has been involved in Japanese eel host response against not only the virus but also the bacterial infection. The full-length cDNA of AjIFN (826 bp) has an ORF of 531 bp. The analysis of NCBI CDD showed that the AjIFN protein had the typical conserved domains, including IFabd conserved domain, and two conserved cysteine residues potentially forming disulphide bridges. Based on the phylogenetic analysis, AjIFN was classified into type I IFNs families belonging to the subgroup-a of the 2Cys group. In vivo, the AjIFN expressions in liver and kidney were induced following injection with LPS, the viral mimic poly I:C, and Aeromonas hydrophila infection. In vitro, the AjIFN transcripts of Japanese eel liver cells were enhanced by LPS, poly I:C and CpG-DNA stimulation and no change of the expression level was found post PGN treatment. Following A. hydrophila infection, the low concentration of 1 × 106 cfu/mL failed to induce the expression of AjIFN whereas the concentration of 1 × 107 cfu/mL and 1 × 108 cfu/mL successfully induced the expression of AjIFN. These results collectively suggested AjIFN is an inducible gene possibly involved in Japanese eel defense against viral and bacterial infection.
Agri GeneAgricultural and Biological Sciences-Agricultural and Biological Sciences (miscellaneous)
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期刊介绍:
Agri Gene publishes papers that focus on the regulation, expression, function and evolution of genes in crop plants, farm animals, and agriculturally important insects and microorganisms. Agri Gene strives to be a diverse journal and topics in multiple fields will be considered for publication so long as their main focus is on agriculturally important organisms (plants, animals, insects, or microorganisms). Although not limited to the following, some examples of potential topics include: Gene discovery and characterization. Genetic markers to guide traditional breeding. Genetic effects of transposable elements. Evolutionary genetics, molecular evolution, population genetics, and phylogenetics. Profiling of gene expression and genetic variation. Biotechnology and crop or livestock improvement. Genetic improvement of biological control microorganisms. Genetic control of secondary metabolic pathways and metabolic enzymes of crop pathogens. Transcription analysis of beneficial or pest insect developmental stages Agri Gene encourages submission of novel manuscripts that present a reasonable level of analysis, functional relevance and/or mechanistic insight. Agri Gene also welcomes papers that have predominantly a descriptive component but improve the essential basis of knowledge for subsequent functional studies, or which provide important confirmation of recently published discoveries provided that the information is new.