Transcriptional responses of liver and spleen in Lota lota to polyriboinosinic polyribocytidylic acid
IntroductionThe cultured Lota lota can meet the market demand in the context of the decline of wild resources, but the disease in the high-density culture process also deserves attention. Therefore, understanding the immune regulation mechanisms of L. lota will be the basis for obtaining high benefi...
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ftdoajarticles:oai:doaj.org/article:cc4ed725c6144c0fa64ef4c2d95b7865 2023-11-12T04:20:46+01:00 Transcriptional responses of liver and spleen in Lota lota to polyriboinosinic polyribocytidylic acid Fangrui Lou Yuan Zhang Anle Xu Tianxiang Gao 2023-10-01T00:00:00Z https://doi.org/10.3389/fimmu.2023.1272393 https://doaj.org/article/cc4ed725c6144c0fa64ef4c2d95b7865 EN eng Frontiers Media S.A. https://www.frontiersin.org/articles/10.3389/fimmu.2023.1272393/full https://doaj.org/toc/1664-3224 1664-3224 doi:10.3389/fimmu.2023.1272393 https://doaj.org/article/cc4ed725c6144c0fa64ef4c2d95b7865 Frontiers in Immunology, Vol 14 (2023) Lota lota liver spleen transcriptome poly (I:C) viral response mechanism Immunologic diseases. Allergy RC581-607 article 2023 ftdoajarticles https://doi.org/10.3389/fimmu.2023.1272393 2023-10-15T00:36:07Z IntroductionThe cultured Lota lota can meet the market demand in the context of the decline of wild resources, but the disease in the high-density culture process also deserves attention. Therefore, understanding the immune regulation mechanisms of L. lota will be the basis for obtaining high benefits in artificial culture.MethodsTo explore the viral response mechanism of L. lota, RNA-seq was applied to identify the transcriptomic changes of the liver and spleen in L. lota by poly (I:C) stress.ResultsThe DEGs (liver: 2186 to 3123; spleen 1542 to 2622) and up-regulated genes (liver: 1231 to 1776; spleen 769 to 1502) in the liver and spleen increased with the prolongation (12h to 48h) of poly (I:C)-stimulation time. This means L. lota needs to mobilize more functional genes in response to longer periods of poly (I:C)-stimulation. Despite the responses of L. lota to poly (I:C) showed tissue-specificity, we hypothesized that both liver and spleen of L. lota can respond to poly (I:C) challenge may be through promoting apoptosis of DNA-damaged cells, increasing the activity of immune-enhancing enzymes, and increasing energy supply based on DEGs annotation information.ConclusionsOur results demonstrate the transcriptional responses of L. lota to poly (I:C)-stimulation, and these data provide the first resource on the genetic regulation mechanisms of L. lota against viruses. Furthermore, the present study can provide basic information for the prevention of viral diseases in L. lota artificial culture process. Article in Journal/Newspaper Lota lota lota Directory of Open Access Journals: DOAJ Articles Frontiers in Immunology 14 |
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Open Polar |
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Directory of Open Access Journals: DOAJ Articles |
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English |
topic |
Lota lota liver spleen transcriptome poly (I:C) viral response mechanism Immunologic diseases. Allergy RC581-607 |
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Lota lota liver spleen transcriptome poly (I:C) viral response mechanism Immunologic diseases. Allergy RC581-607 Fangrui Lou Yuan Zhang Anle Xu Tianxiang Gao Transcriptional responses of liver and spleen in Lota lota to polyriboinosinic polyribocytidylic acid |
topic_facet |
Lota lota liver spleen transcriptome poly (I:C) viral response mechanism Immunologic diseases. Allergy RC581-607 |
description |
IntroductionThe cultured Lota lota can meet the market demand in the context of the decline of wild resources, but the disease in the high-density culture process also deserves attention. Therefore, understanding the immune regulation mechanisms of L. lota will be the basis for obtaining high benefits in artificial culture.MethodsTo explore the viral response mechanism of L. lota, RNA-seq was applied to identify the transcriptomic changes of the liver and spleen in L. lota by poly (I:C) stress.ResultsThe DEGs (liver: 2186 to 3123; spleen 1542 to 2622) and up-regulated genes (liver: 1231 to 1776; spleen 769 to 1502) in the liver and spleen increased with the prolongation (12h to 48h) of poly (I:C)-stimulation time. This means L. lota needs to mobilize more functional genes in response to longer periods of poly (I:C)-stimulation. Despite the responses of L. lota to poly (I:C) showed tissue-specificity, we hypothesized that both liver and spleen of L. lota can respond to poly (I:C) challenge may be through promoting apoptosis of DNA-damaged cells, increasing the activity of immune-enhancing enzymes, and increasing energy supply based on DEGs annotation information.ConclusionsOur results demonstrate the transcriptional responses of L. lota to poly (I:C)-stimulation, and these data provide the first resource on the genetic regulation mechanisms of L. lota against viruses. Furthermore, the present study can provide basic information for the prevention of viral diseases in L. lota artificial culture process. |
format |
Article in Journal/Newspaper |
author |
Fangrui Lou Yuan Zhang Anle Xu Tianxiang Gao |
author_facet |
Fangrui Lou Yuan Zhang Anle Xu Tianxiang Gao |
author_sort |
Fangrui Lou |
title |
Transcriptional responses of liver and spleen in Lota lota to polyriboinosinic polyribocytidylic acid |
title_short |
Transcriptional responses of liver and spleen in Lota lota to polyriboinosinic polyribocytidylic acid |
title_full |
Transcriptional responses of liver and spleen in Lota lota to polyriboinosinic polyribocytidylic acid |
title_fullStr |
Transcriptional responses of liver and spleen in Lota lota to polyriboinosinic polyribocytidylic acid |
title_full_unstemmed |
Transcriptional responses of liver and spleen in Lota lota to polyriboinosinic polyribocytidylic acid |
title_sort |
transcriptional responses of liver and spleen in lota lota to polyriboinosinic polyribocytidylic acid |
publisher |
Frontiers Media S.A. |
publishDate |
2023 |
url |
https://doi.org/10.3389/fimmu.2023.1272393 https://doaj.org/article/cc4ed725c6144c0fa64ef4c2d95b7865 |
genre |
Lota lota lota |
genre_facet |
Lota lota lota |
op_source |
Frontiers in Immunology, Vol 14 (2023) |
op_relation |
https://www.frontiersin.org/articles/10.3389/fimmu.2023.1272393/full https://doaj.org/toc/1664-3224 1664-3224 doi:10.3389/fimmu.2023.1272393 https://doaj.org/article/cc4ed725c6144c0fa64ef4c2d95b7865 |
op_doi |
https://doi.org/10.3389/fimmu.2023.1272393 |
container_title |
Frontiers in Immunology |
container_volume |
14 |
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1782336550186516480 |