Transcriptomic analyses provide new insights into immune response of the Procambarus clarkii intestines to Aeromonas hydrophila challenge

被引:2
|
作者
Liu, Xin [1 ,2 ,3 ]
Bian, Dan -Dan [1 ]
Jiang, Jun-Jie [1 ,3 ]
Tang, Sheng [1 ,3 ]
Lu, Xiang [1 ,3 ]
Zhang, Dai-Zhen [3 ]
Liu, Qiu-Ning [3 ]
Tang, Bo-Ping [3 ]
Dai, Li-Shang [2 ]
机构
[1] Shanghai Ocean Univ, Coll Aquaculture & Life Sci, Key Lab Freshwater Aquat Genet Resources, Minist Agr & Rural Affairs, Shanghai, Peoples R China
[2] Wenzhou Med Univ, Sch Pharmaceut Sci, Wenzhou 325035, Peoples R China
[3] Yancheng Teachers Univ, Jiangsu Synthet Innovat Ctr Coastal Bioagr, Jiangsu Key Lab Bioresources Saline Soils, Jiangsu Prov Key Lab Coastal Wetland Bioresources, Yancheng, Peoples R China
关键词
Procambarus clarkii; Gene expression; Aeromonas hydrophila; Immune defense mechanism; Transcriptome; RED SWAMP CRAYFISH; PATTERN-RECOGNITION RECEPTOR; TYROSINE METABOLISM; I CRUSTIN; LYSOZYME; PROTEINS; IDENTIFICATION; PHENOLOXIDASE; BIOSYNTHESIS; ACCUMULATION;
D O I
10.1016/j.aqrep.2024.102103
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
In recent years, the death rate of Procambarus clarkii increased sharply due to pathogenic bacterial infections, leading to huge economic losses. To determine the immune response of the intestinal tissues of P. clarkii to bacterial infections, we compared the immune indexes, histopathological damage, and transcriptome data of the control and Aeromonas hydrophila -infected P. clarkii . With the injection of A. hydrophila , it was found that intestinal mucosal folds increased, intestinal villi showed obvious vacuolation, and the tissue structure changed significantly. The results of non-specific immunoenzyme activity showed that the Total protein (TP) content was significantly lower than that of the control group at 24 h, and the Acid phosphatase (ACP) and Alkaline phosphatase (AKP) activities in the treatment group showed a significant increasing trend ( p < 0.05). In terms of the transcriptome, an average of 22,927,523 clean reads and 27,866 genes were found in the control and treatment groups through gene assembly and annotation. Among these genes, 567 were identified as differentially expressed genes (DEGs), of which 501 were up-regulated and 66 were down-regulated. Quantitative-polymerase chain reaction (qPCR) analysis of six randomly selected genes was used to verify the RNA-sequencing results. The Gene Ontology enrichment analysis revealed that the DEGs were primarily involved in cell processes, metabolic processes, and biological regulation, while the Kyoto Encyclopedia of Genes and Genomes enrichment analysis showed that these DEGs were involved in tyrosine metabolism, glycosphingolipid biosynthesis -ganglionic series, and nitrogen metabolism. We studied the tyrosine metabolic pathway and found that it contributes to the immune defense mechanism of P. clarkii . The results of our study provide important insights into the intestinal immune response of P. clarkii to A. hydrophila infection.
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页数:13
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