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Hepatopancreas immune response during molt cycle in the mud crab, Scylla paramamosain

Molt is a critical developmental process in crustaceans. Recent studies have shown that the hepatopancreas is an important source of innate immune molecules, yet hepatopancreatic patterns of gene expression during the molt cycle which may underlie changes in immune mechanism are unknown. In this stu...

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Autores principales: Xu, Zhanning, Liu, An, Li, Shengkang, Wang, Guizhong, Ye, Haihui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7403367/
https://www.ncbi.nlm.nih.gov/pubmed/32753724
http://dx.doi.org/10.1038/s41598-020-70139-2
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author Xu, Zhanning
Liu, An
Li, Shengkang
Wang, Guizhong
Ye, Haihui
author_facet Xu, Zhanning
Liu, An
Li, Shengkang
Wang, Guizhong
Ye, Haihui
author_sort Xu, Zhanning
collection PubMed
description Molt is a critical developmental process in crustaceans. Recent studies have shown that the hepatopancreas is an important source of innate immune molecules, yet hepatopancreatic patterns of gene expression during the molt cycle which may underlie changes in immune mechanism are unknown. In this study, we performed Illumina sequencing for the hepatopancreas of the mud crab, Scylla paramamosain during molt cycle (pre-molt stage, post-molt stage, and inter-molt stage). A total of 44.55 Gb high-quality reads were obtained from the normalized cDNA of hepatopancreas. A total of 70,591 transcripts were assembled; 55,167 unigenes were identified. Transcriptomic comparison revealed 948 differentially expressed genes (DEGs) in the hepatopancreas from the three molt stages. We found that genes associated with immune response patterns changed in expression during the molt cycle. Antimicrobial peptide genes, inflammatory response genes, Toll signaling pathway factors, the phenoloxidase system, antioxidant enzymes, metal-binding proteins and other immune related genes are significantly up-regulated at the post-molt stage and inter-molt stage compared with the pre-molt stage, respectively. These genes are either not expressed or are expressed at low levels at the pre-molt stage. To our knowledge, this is the first systematic transcriptome analysis of genes capable of mobilizing a hepatopancreas immune response during the molt cycle in crustaceans, and this study will contribute to a better understanding of the hepatopancreas immune system and mud crab prophylactic immune mechanisms at the post-molt stage.
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spelling pubmed-74033672020-08-07 Hepatopancreas immune response during molt cycle in the mud crab, Scylla paramamosain Xu, Zhanning Liu, An Li, Shengkang Wang, Guizhong Ye, Haihui Sci Rep Article Molt is a critical developmental process in crustaceans. Recent studies have shown that the hepatopancreas is an important source of innate immune molecules, yet hepatopancreatic patterns of gene expression during the molt cycle which may underlie changes in immune mechanism are unknown. In this study, we performed Illumina sequencing for the hepatopancreas of the mud crab, Scylla paramamosain during molt cycle (pre-molt stage, post-molt stage, and inter-molt stage). A total of 44.55 Gb high-quality reads were obtained from the normalized cDNA of hepatopancreas. A total of 70,591 transcripts were assembled; 55,167 unigenes were identified. Transcriptomic comparison revealed 948 differentially expressed genes (DEGs) in the hepatopancreas from the three molt stages. We found that genes associated with immune response patterns changed in expression during the molt cycle. Antimicrobial peptide genes, inflammatory response genes, Toll signaling pathway factors, the phenoloxidase system, antioxidant enzymes, metal-binding proteins and other immune related genes are significantly up-regulated at the post-molt stage and inter-molt stage compared with the pre-molt stage, respectively. These genes are either not expressed or are expressed at low levels at the pre-molt stage. To our knowledge, this is the first systematic transcriptome analysis of genes capable of mobilizing a hepatopancreas immune response during the molt cycle in crustaceans, and this study will contribute to a better understanding of the hepatopancreas immune system and mud crab prophylactic immune mechanisms at the post-molt stage. Nature Publishing Group UK 2020-08-04 /pmc/articles/PMC7403367/ /pubmed/32753724 http://dx.doi.org/10.1038/s41598-020-70139-2 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Xu, Zhanning
Liu, An
Li, Shengkang
Wang, Guizhong
Ye, Haihui
Hepatopancreas immune response during molt cycle in the mud crab, Scylla paramamosain
title Hepatopancreas immune response during molt cycle in the mud crab, Scylla paramamosain
title_full Hepatopancreas immune response during molt cycle in the mud crab, Scylla paramamosain
title_fullStr Hepatopancreas immune response during molt cycle in the mud crab, Scylla paramamosain
title_full_unstemmed Hepatopancreas immune response during molt cycle in the mud crab, Scylla paramamosain
title_short Hepatopancreas immune response during molt cycle in the mud crab, Scylla paramamosain
title_sort hepatopancreas immune response during molt cycle in the mud crab, scylla paramamosain
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7403367/
https://www.ncbi.nlm.nih.gov/pubmed/32753724
http://dx.doi.org/10.1038/s41598-020-70139-2
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