Immune-related miRNA-mRNA regulation network in the livers of DHAV-3-infected ducklings

被引:17
作者
Wu, Fengyao [1 ,2 ]
Lu, Fengying [1 ,2 ]
Fan, Xin [1 ,3 ]
Chao, Jin [1 ,4 ]
Liu, Chuanmin [1 ,2 ]
Pan, Qunxing [1 ,2 ]
Sun, Huawei [1 ,2 ]
Zhang, Xiaofei [1 ,2 ]
机构
[1] Jiangsu Acad Agr Sci, Inst Vet Med, Nanjing, Jiangsu, Peoples R China
[2] Minist Agr, Key Lab Vet Biol Engn & Technol, Nanjing, Jiangsu, Peoples R China
[3] Tibet Agr & Anim Husb Univ, Acad Anim Sci, Linzhi, TN, Peoples R China
[4] Anhui Agr Univ, Coll Anim Sci & Technol, Hefei, Anhui, Peoples R China
基金
中国博士后科学基金; 国家重点研发计划;
关键词
Duck hepatitis a virus type 3; miRNA; Transcriptome; miRNA-mRNA network; Innate immune response; Host-virus interactions; TOLL-LIKE RECEPTORS; VIRUS TYPES 1; MICRORNAS; EXPRESSION; DISEASE; REPLICATION; CONTRIBUTES; SUPPRESSION; INFECTION; RESPONSES;
D O I
10.1186/s12864-020-6539-7
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background Duck hepatitis A virus type 3 (DHAV-3) is one of the most harmful pathogens in the duck industry. However, the molecular mechanism underlying DHAV-3 infection in ducklings remains poorly understood. To study the genetic regulatory network for miRNA-mRNA and the signaling pathways involved in DHAV-3 infection in ducklings, we conducted global miRNA and mRNA expression profiling of duckling liver tissues infected with lethal DHAV-3 by high-throughput sequencing. Results We found 156 differentially expressed miRNAs (DEMs) and 7717 differentially expressed genes (DEGs) in livers of mock-infected and DHAV-3-infected duckling. A total of 19,606 miRNA-mRNA pairs with negatively correlated expression patterns were identified in miRNA-mRNA networks constructed on the basis of these DEMs and DEGs. Moreover, immune-related pathways, including the cytokine-cytokine receptor interaction, apoptosis, Toll-like receptor, Jak-STAT, and RIG-I-like receptor signaling pathway, were significantly enriched through analyzing functions of mRNAs in the network in response to DHAV-3 infection. Furthermore, apl-miR-32-5p, apl-miR-125-5p, apl-miR-128-3p, apl-miR-460-5p, and novel-m0012-3p were identified as potential regulators in the immune-related signaling pathways during DHAV-3 infection. And some host miRNAs were predicted to target the DHAV-3 genome. Conclusions This is the first integrated analysis of miRNA and mRNA in DHAV-3-infected ducklings. The results indicated the important roles of miRNAs in regulating immune response genes and revealed the immune related miRNA-mRNA regulation network in the DHAV-3-infected duckling liver. These findings increase our knowledge of the roles of miRNAs and their target genes in DHAV-3 replication and pathogenesis. They also aid in the understanding of host-virus interactions.
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页数:14
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