Literature DB >> 22796486

Expression profiles of NODs in channel catfish (Ictalurus punctatus) after infection with Edwardsiella tarda, Aeromonas hydrophila, Streptococcus iniae and channel catfish hemorrhage reovirus.

Min Li1, Qi-long Wang, Yang Lu, Song-lin Chen, Qi Li, Zhen-xia Sha.   

Abstract

NLRs are a large family of intracellular pathogen recognition receptors (PRRs) that recognize pathogen associated molecular patterns (PAMPs). In the previous study, the identification of NLRs subfamily A (NODs) and gene expression was carried out in channel catfish (Ictalurus punctatus). However, the gene expression profiles of channel catfish NODs (NOD1, NOD2, NLRC3, NLRC5 and NLRX1) after infection with various bacteria and virus are still unclear. In this study, expression of five NODs genes was analyzed by quantitative real-time PCR method. In healthy catfish tissues, all tested NODs genes were found to be ubiquitously expressed. After infection with Edwardsiella tarda, Aeromonas hydrophila, Streptococcus iniae, or channel catfish hemorrhage reovirus (CCRV), expression of NOD1, NOD2, NLRC3, NLRC5 showed a significant up-regulation in the intestine, liver and head kidney, whereas down-regulation was observed in the spleen after infection with A. hydrophila and CCRV. Expression of NLRX1 gene was up-regulated in the intestine, liver and head kidney, while obviously decreased in the spleen after infection with four pathogens. Among four different pathogens, S. iniae largely up-regulated NODs mRNAs, while CCRV only slightly enhanced NODs gene expression. Among four immune-related tissues, the order for NODs up-regulation was liver, head kidney, intestine, and spleen after infection with various pathogens. All data suggest NODs are involved in the immune responses of channel catfish against the intracellular bacterial and virus pathogens in tissue-specific and pathogen-specific manners, and provide the evidence for exploring the precise immune-related molecular mechanism of NODs in channel catfish.
Copyright © 2012 Elsevier Ltd. All rights reserved.

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Year:  2012        PMID: 22796486     DOI: 10.1016/j.fsi.2012.06.033

Source DB:  PubMed          Journal:  Fish Shellfish Immunol        ISSN: 1050-4648            Impact factor:   4.581


  8 in total

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Authors:  Yi Wei Hu; Xiao Man Wu; Shi Si Ren; Lu Cao; Pin Nie; Ming Xian Chang
Journal:  Sci Rep       Date:  2017-06-07       Impact factor: 4.379

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Journal:  Front Immunol       Date:  2021-12-15       Impact factor: 8.786

Review 6.  A Comparative Review of Pyroptosis in Mammals and Fish.

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Authors:  Shenji Wu; Jinqiang Huang; Yongjuan Li; Mingquan Lei; Lu Zhao; Zhe Liu
Journal:  Front Immunol       Date:  2022-09-02       Impact factor: 8.786

8.  Transcriptome-wide mapping of signaling pathways and early immune responses in lumpfish leukocytes upon in vitro bacterial exposure.

Authors:  Håvard Ø Eggestøl; Harald S Lunde; Anita Rønneseth; David Fredman; Kjell Petersen; Charitra K Mishra; Tomasz Furmanek; Duncan J Colquhoun; Heidrun I Wergeland; Gyri T Haugland
Journal:  Sci Rep       Date:  2018-03-27       Impact factor: 4.379

  8 in total

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