Abstract

Orf, caused by Orf virus (ORFV), is a globally distributed zoonotic disease responsible for serious economic losses in the agricultural sector. However, the mechanism underlying ORFV infection remains largely unknown. Circular RNAs (circRNAs), a novel type of endogenous non-coding RNAs, play important roles in various pathological processes but their involvement in ORFV infection and host response is unclear. In the current study, whole transcriptome sequencing and small RNA sequencing were performed in ORFV-infected goat skin fibroblast cells and uninfected cells. A total of 151 circRNAs, 341 messenger RNAs (mRNAs), and 56 microRNAs (miRNAs) were differently expressed following ORFV infection. Four circRNAs: circRNA1001, circRNA1684, circRNA3127 and circRNA7880 were validated by qRT-PCR and Sanger sequencing. Gene ontology (GO) analysis indicated that host genes of differently expressed circRNAs were significantly enriched in regulation of inflammatory response, epithelial structure maintenance, positive regulation of cell migration, positive regulation of ubiquitin-protein transferase activity, regulation of ion transmembrane transport, etc. The constructed circRNA-miRNA-mRNA network suggested that circRNAs may function as miRNA sponges indirectly regulating gene expression following ORFV infection. Our study presented the first comprehensive profiles of circRNAs in response to ORFV infection, thus providing new clues for the mechanisms of interactions between ORFV and the host.

Highlights

  • Circular RNAs, a new member of non-coding RNAs, are generally produced by back-splicing of pre-messenger RNAs (mRNAs)(Barrett & Salzman, 2016; Barrett, Wang & Salzman, 2015)

  • We aligned the reads unmapped to goat genome from each sample to Orf virus reference genome (Orf virus NA1/11 strain under GenBank number KF234407.1)

  • The results indicated that a total of 125,619 reads, 165,878 reads and 157,779 reads were mapped to Orf virus genome in ORFV infected GSF samples (OV)-1, OV-2, and OV-3 sample, respectively

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Summary

Introduction

Circular RNAs (circRNAs), a new member of non-coding RNAs, are generally produced by back-splicing of pre-mRNA(Barrett & Salzman, 2016; Barrett, Wang & Salzman, 2015). Because of their unique circular structure, circRNAs can resist the activity of RNA exonuclease digestion. They are more stable and have longer half-lives than their linear transcripts in vivo (Jeck et al, 2013; Suzuki et al, 2006).

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