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MicroRNA Expression Profile in Peripheral Blood Lymphocytes of Sheep Vaccinated with Nigeria 75/1 Peste Des Petits Ruminants Virus

机译:接种尼日利亚75/1 Peste Des小反刍动物病毒的绵羊外周血淋巴细胞中MicroRNA表达谱

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摘要

Peste des petits ruminants (PPR) is one of the highly contagious transboundary viral diseases of small ruminants. Host microRNA (miRNA) expression patterns may change in response to virus infection, and it mainly works as a post-transcriptional moderator in gene expression and affects viral pathogenesis and replication. In this study, the change of miRNA expression profile in peripheral blood lymphocyte (PBMC) from sheep inoculated with PPR vaccine virus in vivo as well as primary sheep testicular (ST) cells inoculated with PPR vaccine virus in vitro were determined via deep sequencing technology. In PBMC cells, 373 and 115 differentially expressed miRNAs (DEmiRNAs) were identified 3 days and 5 days post inoculated (dpi), respectively. While, 575 DEmiRNAs were identified when comparing miRNA profiles on 5 dpi with 3 dpi. Some of the DEmiRNAs were found to change significantly via time-course during PPR vaccine virus inoculated. Similarly, in ST cells, 136 DEmiRNAs were identified at 3 dpi in comparison with mock-inoculation. A total of 12 DEmiRNAs were validated by real-time quantitative PCR (RT-qPCR). The oar-miR-150, oar-miR-370-3p and oar-miR-411b-3p were found common differentially expressed in both PPR vaccine virus-inoculated PBMC cells and ST cells. Targets prediction and functional analysis of the DEmiRNAs uncovered mainly gathering in antigen processing and presentation pathways, protein processing in endoplasmic reticulum pathways and cell adhesion molecules pathways. Our study supplies information about the DEmiRNAs in PPR vaccine virus-inoculated PBMC cells and ST cells, and provides clues for further understanding the function of miRNAs in PPR vaccine virus replication.
机译:小反刍兽疫(PPR)是小反刍动物高度传染性的跨界病毒性疾病之一。宿主microRNA(miRNA)的表达模式可能会因病毒感染而发生变化,并且主要充当基因表达的转录后调节剂,并影响病毒的发病机理和复制。在这项研究中,通过深度测序技术确定了体内接种PPR疫苗病毒的绵羊外周血淋巴细胞(PBMC)以及体外接种PPR疫苗病毒的原代绵羊睾丸(ST)细胞中miRNA表达谱的变化。在PBMC细胞中,分别在接种后3天和5天(dpi)鉴定出373和115个差异表达的miRNA(DEmiRNA)。同时,比较5 dpi和3 dpi的miRNA图谱时,鉴定出575个DEmiRNA。在接种PPR疫苗病毒期间,发现某些DEmiRNA随时间发生显着变化。同样,在ST细胞中,与模拟接种相比,在3 dpi下鉴定出136个DEmiRNA。通过实时定量PCR(RT-qPCR)验证了总共12个DEmiRNA。发现在PPR疫苗病毒接种的PBMC细胞和ST细胞中,oar-miR-150,oar-miR-370-3p和oar-miR-411b-3p共同差异表达。发现的DEmiRNA的目标预测和功能分析主要集中在抗原加工和呈递途径,内质网途径和细胞粘附分子途径中的蛋白质加工。我们的研究提供了有关接种PPR疫苗病毒的PBMC细胞和ST细胞中DEmiRNA的信息,并为进一步了解miRNA在PPR疫苗病毒复制中的功能提供了线索。

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