Characterization of two tripartite motif-containing genes from Asian Seabass Lates calcarifer and their expression in response to virus infection and microbial molecular motifs

© 2023 American Fisheries Society.

Bibliographische Detailangaben
Veröffentlicht in:Journal of aquatic animal health. - 1998. - 35(2023), 3 vom: 01. Sept., Seite 169-186
1. Verfasser: Raji Sathyan, Krishnapriya (VerfasserIn)
Weitere Verfasser: Premraj, Avinash, Thavarool Puthiyedathu, Sajeevan
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2023
Zugriff auf das übergeordnete Werk:Journal of aquatic animal health
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Lates calcarifer TRIM21 TRIM39 RGNNV Zymosan A poly(I:C) Pathogen-Associated Molecular Pattern Molecules Zymosan mehr... 9010-72-4 Fish Proteins Poly I-C O84C90HH2L Antiviral Agents
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100 1 |a Raji Sathyan, Krishnapriya  |e verfasserin  |4 aut 
245 1 0 |a Characterization of two tripartite motif-containing genes from Asian Seabass Lates calcarifer and their expression in response to virus infection and microbial molecular motifs 
264 1 |c 2023 
336 |a Text  |b txt  |2 rdacontent 
337 |a ƒaComputermedien  |b c  |2 rdamedia 
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500 |a Date Completed 23.10.2023 
500 |a Date Revised 30.10.2023 
500 |a published: Print-Electronic 
500 |a RefSeq: MN516801.1 
500 |a Citation Status MEDLINE 
520 |a © 2023 American Fisheries Society. 
520 |a OBJECTIVE: We identified two tripartite motif (TRIM) genes, LcTRIM21 and LcTRIM39, from the Asian Seabass Lates calcarifer, and examined their responses to experimental betanodavirus infection and stimulation with microbial pathogen-associated molecular patterns 
520 |a METHODS: Genes encoding LcTRIM21 and LcTRIM39 were identified, cloned, and sequenced from the Asian Seabass. We analyzed the sequence using a variety of bioinformatics tools to determine protein structure, localization, and establish a phylogenetic tree. By using quantitative real-time PCR, we analyzed expression profiles of the LcTRIM21 and LcTRIM39 genes in response to betanodavirus challenge as well as molecular pathogen-associated molecular patterns like poly(I:C) and Zymosan A. The tissue distribution pattern of these genes was also examined in healthy animals 
520 |a RESULT: Asian Seabass homologues of the TRIM gene, LcTRIM21 and LcTRIM39, were cloned, both encoding proteins with 547 amino acids. LcTRIM21 is predicted to have an isoelectric point of 6.32 and a molecular mass of 62.11 kilodaltons, while LcTRIM39 has an isoelectric point of 5.57 and a molecular mass of 62.11 kilodaltons. LcTRIM21 and LcTRIM39 homologues were predicted to be localized in cytoplasm by in silico protein localization. Structurally, both proteins contain an N-terminal really interesting new gene (RING) zinc-finger domain, B-box domain, coiled-coil domain and C-terminal PRY/SPRY domain. Most tissues and organs examined showed constitutive expression of LcTRIM21 and LcTRIM39. Upon poly(I:C) challenge or red-spotted grouper nervous necrosis virus infection, LcTRIM21 and LcTRIM39 mRNA expression was significantly upregulated, suggesting that they may play a critical antiviral role against fish viruses. LcTRIM21 and LcTRIM39 expression were also upregulated by administration of the glucan Zymosan A 
520 |a CONCLUSION: The TRIM-containing gene is an E3 ubiquitin ligase that exhibits antiviral activity by targeting viral proteins via proteasome-mediated ubiquitination. TRIM proteins can be explored for the discovery of antivirals and strategies to combat diseases like viral nervous necrosis, that threaten seabass aquaculture 
650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
650 4 |a Lates calcarifer 
650 4 |a TRIM21 
650 4 |a TRIM39 
650 4 |a RGNNV 
650 4 |a Zymosan A 
650 4 |a poly(I:C) 
650 7 |a Pathogen-Associated Molecular Pattern Molecules  |2 NLM 
650 7 |a Zymosan  |2 NLM 
650 7 |a 9010-72-4  |2 NLM 
650 7 |a Fish Proteins  |2 NLM 
650 7 |a Poly I-C  |2 NLM 
650 7 |a O84C90HH2L  |2 NLM 
650 7 |a Antiviral Agents  |2 NLM 
700 1 |a Premraj, Avinash  |e verfasserin  |4 aut 
700 1 |a Thavarool Puthiyedathu, Sajeevan  |e verfasserin  |4 aut 
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773 1 8 |g volume:35  |g year:2023  |g number:3  |g day:01  |g month:09  |g pages:169-186 
856 4 0 |u http://dx.doi.org/10.1002/aah.10187  |3 Volltext 
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