Li Na, Yan Yunhuan, Zhang Angke, Gao Jiming, Zhang Chong, Wang Xue, Hou Gaopeng, Zhang Gaiping, Jia Jinbu, Zhou En-Min, Xiao Shuqi
College of Veterinary Medicine, Northwest A&F University, Yangling, Shaanxi 712100, China.
Experimental Station of Veterinary Pharmacology and Veterinary Biotechnology, Ministry of Agriculture, Yangling, Shaanxi 712100, China.
Oncotarget. 2016 Dec 13;7(50):82902-82920. doi: 10.18632/oncotarget.12703.
Many viruses encode microRNAs (miRNAs) that are small non-coding single-stranded RNAs which play critical roles in virus-host interactions. Porcine reproductive and respiratory syndrome virus (PRRSV) is one of the most economically impactful viruses in the swine industry. The present study sought to determine whether PRRSV encodes miRNAs that could regulate PRRSV replication. Four viral small RNAs (vsRNAs) were mapped to the stem-loop structures in the ORF1a, ORF1b and GP2a regions of the PRRSV genome by bioinformatics prediction and experimental verification. Of these, the structures with the lowest minimum free energy (MFE) values predicted for PRRSV-vsRNA1 corresponded to typical stem-loop, hairpin structures. Inhibition of PRRSV-vsRNA1 function led to significant increases in viral replication. Transfection with PRRSV-vsRNA1 mimics significantly inhibited PRRSV replication in primary porcine alveolar macrophages (PAMs). The time-dependent increase in the abundance of PRRSV-vsRNA1 mirrored the gradual upregulation of PRRSV RNA expression. Knockdown of proteins associated with cellular miRNA biogenesis demonstrated that Drosha and Argonaute (Ago2) are involved in PRRSV-vsRNA1 biogenesis. Moreover, PRRSV-vsRNA1 bound specifically to the nonstructural protein 2 (NSP2)-coding sequence of PRRSV genome RNA. Collectively, the results reveal that PRRSV encodes a functional PRRSV-vsRNA1 which auto-regulates PRRSV replication by directly targeting and suppressing viral NSP2 gene expression. These findings not only provide new insights into the mechanism of the pathogenesis of PRRSV, but also explore a potential avenue for controlling PRRSV infection using viral small RNAs.
许多病毒编码微小RNA(miRNA),它们是小的非编码单链RNA,在病毒与宿主的相互作用中发挥关键作用。猪繁殖与呼吸综合征病毒(PRRSV)是养猪业中经济影响最大的病毒之一。本研究旨在确定PRRSV是否编码可调节PRRSV复制的miRNA。通过生物信息学预测和实验验证,将四种病毒小RNA(vsRNA)定位到PRRSV基因组的ORF1a、ORF1b和GP2a区域的茎环结构上。其中,预测PRRSV-vsRNA1的最低最小自由能(MFE)值的结构对应于典型的茎环、发夹结构。抑制PRRSV-vsRNA1的功能导致病毒复制显著增加。用PRRSV-vsRNA1模拟物转染可显著抑制原代猪肺泡巨噬细胞(PAM)中的PRRSV复制。PRRSV-vsRNA1丰度的时间依赖性增加反映了PRRSV RNA表达的逐渐上调。敲低与细胞miRNA生物合成相关的蛋白质表明,Drosha和AGO2(Argonaute 2)参与PRRSV-vsRNA1的生物合成。此外,PRRSV-vsRNA1与PRRSV基因组RNA的非结构蛋白2(NSP2)编码序列特异性结合。总体而言,结果表明PRRSV编码功能性的PRRSV-vsRNA1,其通过直接靶向和抑制病毒NSP2基因表达来自动调节PRRSV复制。这些发现不仅为PRRSV发病机制提供了新见解,还探索了利用病毒小RNA控制PRRSV感染的潜在途径。