Genome-wide analysis of long noncoding RNA and mRNA profiles in PRRSV-infected porcine alveolar macrophages

被引:12
|
作者
Wu, Junjing [1 ]
Peng, Xianwen [1 ]
Qiao, Mu [1 ]
Zhao, Haizhong [1 ]
Li, Mingbo [1 ]
Liu, Guisheng [1 ]
Mei, Shuqi [1 ]
机构
[1] Hubei Prov Acad Agr Sci, Inst Anim Husb & Vet, Hubei Key Lab Anim Embryo & Mol Breeding, Wuhan 430064, Peoples R China
关键词
RNA-seq; lncRNA; PRRSV; Porcine alveolar macrophages; RESPIRATORY SYNDROME VIRUS; EXPRESSION; QUANTIFICATION; IDENTIFICATION; ANNOTATION; REVEALS; GENE;
D O I
10.1016/j.ygeno.2019.10.024
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
Porcine reproductive and respiratory syndrome (PARS), which is caused by PARS virus (PRRSV), is one of the most globally devastating swine diseases. It is essential to develop new strategy to control PARS via an understanding of mechanisms that PRRSV utilizes to interfere with the host's innate immunity. In this study, we deeply sequenced and analyzed long noncoding RNA (lncRNA) and mRNA expression profiles of the porcine alveolar macrophages (PAMs) after PRRSV infection. 126 lncRNAs and 753 mRNAs were differentially expressed between PRRSV-infected and control PAMs. The co-expressed genes of down-regulated lncRNAs were significantly enriched within NF-kappa B and toll-like receptor signaling pathways. Co-expression network analysis indicated that part of the dysregulated lncRNAs associated with the interferon-induced genes. These dysregulated lncRNAs may play an important role in the host's innate immune responses to PRRSV infection. However, further research is required to characterize the function of these lncRNAs.
引用
收藏
页码:1879 / 1888
页数:10
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