Jiang Jun-Jie, Bian Dan-Dan, Liu Xin, Zhang Dai-Zhen, Liu Qiu-Ning, Tang Bo-Ping, Zhang Mei-Ling
Key Laboratory of Freshwater Aquatic Genetic Resources, Ministry of Agriculture and Rural Affairs, College of Aquaculture and Life Science, Shanghai Ocean University, Shanghai 201306, People's Republic of China; School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou 325035, People's Republic of China; Jiangsu Key Laboratory for Bioresources of Saline Soils, Jiangsu Synthetic Innovation Center for Coastal Bio-agriculture, Jiangsu Provincial Key Laboratory of Coastal Wetland Bioresources and Environmental Protection, School of Wetlands, Yancheng Teachers University, Yancheng 224007, People's Republic of China.
Jiangsu Key Laboratory for Bioresources of Saline Soils, Jiangsu Synthetic Innovation Center for Coastal Bio-agriculture, Jiangsu Provincial Key Laboratory of Coastal Wetland Bioresources and Environmental Protection, School of Wetlands, Yancheng Teachers University, Yancheng 224007, People's Republic of China; Anhui Key Laboratory of Resource Insect Biology and Innovative Utilization, College of Life Sciences, Anhui Agricultural University, Hefei 230036, People's Republic of China.
Comp Biochem Physiol Part D Genomics Proteomics. 2024 Dec;52:101315. doi: 10.1016/j.cbd.2024.101315. Epub 2024 Aug 20.
Procambarus clarkii is an economically important species in China; however, its high mortality rate due to pathogenic bacteria, particularly Vibrio parahaemolyticus, results in significant economic loss. This study aimed to understand the immune response of crayfish to bacterial infection by comparing and analyzing transcriptome data of hepatopancreatic tissue from P. clarkii challenged with V. parahaemolyticus or treated with PBS. Physiological indices (TP, Alb, ACP, and AKP) were analyzed, and tissue sections were prepared. After assembling and annotating the data, 18,756 unigenes were identified. A comparison of the expression levels of these unigenes between the control and V. parahaemolyticus groups revealed 4037 DEGs, with 2278 unigenes upregulated and 1759 downregulated in the V. parahaemolyticus group. GO (Gene Ontology) enrichment analysis shows that the DGEs are mainly enriched in cellular anatomical activity, bindinga and cellular process, enrichment analysis of KEGG (Kyoto Encyclopedia of Genes and Genomes) pathways showed that DGEs were mainly enriched in Base excision repair, Phagosome and Longevity regulating pathway. At the same time, lysosome was also enriched. The phagosome and lysosome pathways play a crucial role in the immune defense of crayfish against V. parahaemolyticus injection that will be highlighted. In addition, the expression levels of six selected immune-related DEGs were measured using qRT-PCR, which validated the results of RNA-seq analysis. This study provides a new perspective on the immune system and defense mechanisms of P. clarkii and a valuable foundation for further investigation of the molecular immune mechanisms of this species.
克氏原螯虾是中国一种具有重要经济价值的物种;然而,其因致病细菌,尤其是副溶血性弧菌导致的高死亡率造成了重大经济损失。本研究旨在通过比较和分析经副溶血性弧菌攻击或用PBS处理的克氏原螯虾肝胰腺组织的转录组数据,了解小龙虾对细菌感染的免疫反应。分析了生理指标(总蛋白、白蛋白、酸性磷酸酶和碱性磷酸酶),并制备了组织切片。在对数据进行组装和注释后,鉴定出18756个单基因。对照组和副溶血性弧菌组之间这些单基因表达水平的比较显示有4037个差异表达基因(DEG),在副溶血性弧菌组中2278个单基因上调,1759个下调。基因本体论(GO)富集分析表明,差异表达基因主要富集在细胞解剖活性、结合和细胞过程中,京都基因与基因组百科全书(KEGG)通路富集分析表明,差异表达基因主要富集在碱基切除修复、吞噬体和寿命调节通路中。同时,溶酶体也有富集。吞噬体和溶酶体通路在小龙虾抵抗副溶血性弧菌注射的免疫防御中起关键作用,这将是重点。此外,使用qRT-PCR测量了六个选定的免疫相关差异表达基因的表达水平,验证了RNA测序分析的结果。本研究为克氏原螯虾的免疫系统和防御机制提供了新的视角,并为进一步研究该物种的分子免疫机制奠定了宝贵的基础。