Zhao Fu-Rong, Su Shuo, Zhou Dong-Hui, Zhou Pei, Xu Ting-Chuan, Zhang Liang-Quan, Cao Nan, Qi Wen-Bao, Zhang Gui-Hong, Li Shou-Jun
State Key Laboratory of Veterinary Etiological Biology, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, Gansu Province 730046, People's Republic of China.
College of Veterinary Medicine, South China Agricultural University, Guangzhou, Guangdong Province 510642, People's Republic of China.
Infect Genet Evol. 2014 Jan;21:367-74. doi: 10.1016/j.meegid.2013.11.019. Epub 2013 Dec 11.
MicroRNAs (miRNAs) are a class of endogenous non-coding small RNAs of 18-22-nucleotides in length that regulate gene expression at the post-transcriptional level. The objective of this study was to examine the differences in the miRNA expression profiles of the lungs and trachea of beagle dogs infected with canine influenza virus (CIV). Total RNA was isolated from lung and trachea tissues of beagle dogs infected and non-infected with H3N2 CIV at 4 dpi. A total of 41,512,315 and 39,107,475 reads were obtained from the lung and trachea, respectively. Out of a total 288 dog miRNAs available in miRBase, 227 and 236 miRNAs were detected in the infected (Fg) and the non-infected lungs (Fc), respectively, whereas 242 miRNAs were detected in both the infected (Qg) and the non-infected trachea (Qc). From these, 34 and 45 miRNAs were differentially expressed in the lungs and trachea between the infected and non-infected dogs, respectively. More miRNAs were highly expressed in the non-infected tissues than in the infected tissues. miR-143 was the most abundantly expressed miRNA in the four samples, followed by let-7. In total, 252, 234, 196 and 235 novel miRNAs were identified in the Fc, Fg, Qc, and Qg groups, respectively. To our knowledge, this is the first study examining the miRNA gene expression in CIV infected dogs using the Solexa sequencing approach. We have revealed the existence of a large number miRNAs that are affected by CIV infection as well as identified some potentially new miRNAs. These findings will help us better understand the host-CIV interaction and its relationship to pathogenesis, as well as contribute to the prevention and control of CIV.
微小RNA(miRNA)是一类内源性非编码小RNA,长度为18 - 22个核苷酸,在转录后水平调节基因表达。本研究的目的是检测感染犬流感病毒(CIV)的比格犬肺和气管中miRNA表达谱的差异。在感染后第4天,从感染和未感染H3N2 CIV的比格犬的肺和气管组织中分离总RNA。分别从肺和气管中获得了总计41,512,315和39,107,475条读数。在miRBase中总共288个犬miRNA中,在感染的肺(Fg)和未感染的肺(Fc)中分别检测到227和236个miRNA,而在感染的气管(Qg)和未感染的气管(Qc)中均检测到242个miRNA。其中,感染犬和未感染犬的肺和气管中分别有34和45个miRNA差异表达。未感染组织中高表达的miRNA比感染组织中的更多。miR - 143是四个样本中表达最丰富的miRNA,其次是let - 7。总共在Fc、Fg、Qc和Qg组中分别鉴定出252、234、196和235个新的miRNA。据我们所知,这是第一项使用Solexa测序方法检测CIV感染犬中miRNA基因表达的研究。我们揭示了大量受CIV感染影响的miRNA的存在,并鉴定出一些潜在的新miRNA。这些发现将有助于我们更好地理解宿主与CIV的相互作用及其与发病机制的关系,也有助于CIV的预防和控制。