Wuxi Fisheries College, Nanjing Agricultural University, Nanjing, 210095, China.
Key Laboratory of Freshwater Fisheries and Germplasm Resources Utilization, Ministry of Agriculture, Freshwater Fisheries Research Center, Chinese Academy of Fishery Sciences, No. 9 Shanshui East Road, Wuxi, 214081, Jiangsu, China.
Sci Rep. 2020 Dec 4;10(1):21225. doi: 10.1038/s41598-020-78191-8.
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.
每年 4 月至 5 月,中国江苏和其他地区养殖的克氏原螯虾(Procambarus clarkii)死亡率较高,这种现象被称为“黑五月”病(BMD)。因此,为了调查该病的可能病因,本研究收集了受 BMD 影响的 P. clarkii 样本,并对其肝胰腺、鳃和肌肉组织进行了转录组分析。分别从受 BMD 影响的 P. clarkii 的鳃、肌肉和肝胰腺中获得了 19995164、149212804 和 222053848 条清洁读段,鉴定出 114024 个基因。鳃、肌肉和肝胰腺中差异表达基因(DEGs)的数量分别为 1703、964 和 476 个。然后对 DEGs 进行了 GO 和 KEGG 富集分析。基于 KEGG 通路富集分析,最显著差异表达的通路主要与代谢、人类疾病和细胞过程有关。对显著 DEGs 的进一步分析表明,它们主要与线粒体介导的细胞凋亡途径有关,这些 DEGs 的表达大多下调。此外,与免疫和代谢相关途径相关的基因的表达也显著下调,这些受到显著抑制的途径可能是 P. clarkii 死亡的原因。因此,我们的结果为鉴定 BMD 病因提供了依据。