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Transcriptomic analysis of Procambarus clarkii affected by “Black May” disease

Each year from April to May, high mortality rates are reported in red swamp crayfish (Procambarus clarkii) cultured in Jiangsu and other regions, in China, and this phenomenon has come to be known as “Black May” disease (BMD). Therefore, in order to investigate the possible causes of this disease, t...

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Autores principales: Shen, Guoqing, Zhang, Xiao, Gong, Jie, Wang, Yang, Huang, Pengdan, Shui, Yan, Xu, Zenghong, Shen, Huaishun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7719172/
https://www.ncbi.nlm.nih.gov/pubmed/33277587
http://dx.doi.org/10.1038/s41598-020-78191-8
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author Shen, Guoqing
Zhang, Xiao
Gong, Jie
Wang, Yang
Huang, Pengdan
Shui, Yan
Xu, Zenghong
Shen, Huaishun
author_facet Shen, Guoqing
Zhang, Xiao
Gong, Jie
Wang, Yang
Huang, Pengdan
Shui, Yan
Xu, Zenghong
Shen, Huaishun
author_sort Shen, Guoqing
collection PubMed
description Each year from April to May, high mortality rates are reported in red swamp crayfish (Procambarus clarkii) cultured in Jiangsu and other regions, in China, and this phenomenon has come to be known as “Black May” disease (BMD). Therefore, in order to investigate the possible causes of this disease, this study gathered BMD-affected P. clarkii samples and performed transcriptome analysis on hepatopancreas, gill, and muscle tissues. A total of 19,995,164, 149,212,804, and 222,053,848 clean reads were respectively obtained from the gills, muscle, and hepatopancreas of BMD-affected P. clarkii, and 114,024 unigenes were identified. The number of differentially expressed genes (DEGs) in gill, muscle, and hepatopancreas was 1703, 964, and 476, respectively. GO and KEGG enrichment analyses of the DEGs were then conducted. Based on KEGG pathway enrichment analysis, the most significantly differentially expressed pathways were mainly those involved with metabolism, human disease, and cellular processes. Further analysis of the significantly DEGs revealed that they were mainly related to the mitochondrial-mediated apoptosis pathway and that the expression of these DEGs was mostly down-regulated. Moreover, the expression of genes related to immune and metabolism-related pathways was also significantly down-regulated, and these significantly-inhibited pathways were the likely causes of P. clarkii death. Therefore, our results provide a basis for the identification of BMD causes.
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spelling pubmed-77191722020-12-08 Transcriptomic analysis of Procambarus clarkii affected by “Black May” disease Shen, Guoqing Zhang, Xiao Gong, Jie Wang, Yang Huang, Pengdan Shui, Yan Xu, Zenghong Shen, Huaishun Sci Rep Article Each year from April to May, high mortality rates are reported in red swamp crayfish (Procambarus clarkii) cultured in Jiangsu and other regions, in China, and this phenomenon has come to be known as “Black May” disease (BMD). Therefore, in order to investigate the possible causes of this disease, this study gathered BMD-affected P. clarkii samples and performed transcriptome analysis on hepatopancreas, gill, and muscle tissues. A total of 19,995,164, 149,212,804, and 222,053,848 clean reads were respectively obtained from the gills, muscle, and hepatopancreas of BMD-affected P. clarkii, and 114,024 unigenes were identified. The number of differentially expressed genes (DEGs) in gill, muscle, and hepatopancreas was 1703, 964, and 476, respectively. GO and KEGG enrichment analyses of the DEGs were then conducted. Based on KEGG pathway enrichment analysis, the most significantly differentially expressed pathways were mainly those involved with metabolism, human disease, and cellular processes. Further analysis of the significantly DEGs revealed that they were mainly related to the mitochondrial-mediated apoptosis pathway and that the expression of these DEGs was mostly down-regulated. Moreover, the expression of genes related to immune and metabolism-related pathways was also significantly down-regulated, and these significantly-inhibited pathways were the likely causes of P. clarkii death. Therefore, our results provide a basis for the identification of BMD causes. Nature Publishing Group UK 2020-12-04 /pmc/articles/PMC7719172/ /pubmed/33277587 http://dx.doi.org/10.1038/s41598-020-78191-8 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Shen, Guoqing
Zhang, Xiao
Gong, Jie
Wang, Yang
Huang, Pengdan
Shui, Yan
Xu, Zenghong
Shen, Huaishun
Transcriptomic analysis of Procambarus clarkii affected by “Black May” disease
title Transcriptomic analysis of Procambarus clarkii affected by “Black May” disease
title_full Transcriptomic analysis of Procambarus clarkii affected by “Black May” disease
title_fullStr Transcriptomic analysis of Procambarus clarkii affected by “Black May” disease
title_full_unstemmed Transcriptomic analysis of Procambarus clarkii affected by “Black May” disease
title_short Transcriptomic analysis of Procambarus clarkii affected by “Black May” disease
title_sort transcriptomic analysis of procambarus clarkii affected by “black may” disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7719172/
https://www.ncbi.nlm.nih.gov/pubmed/33277587
http://dx.doi.org/10.1038/s41598-020-78191-8
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