Abstract

Ovine progressive pneumonia virus (OPPV) is an important virus that causes serious diseases in sheep and goats with a prevalence of 36% in the USA. Although OPPV was discovered more than half of a century ago, little is known about the infection and pathogenesis of this virus. In this report, we used RNA-seq technology to conduct a genome-wide probe for cellular factors that are associated with OPPV infection. A total of approximately 22,000 goat host genes were detected of which 657 were found to have been significantly up-regulated and 889 down-regulated at 12 hours post-infection. In addition to previously known restriction factors from other viral infections, a number of factors which may be specific for OPPV infection were uncovered. The data from this RNA-seq study will be helpful in our understanding of OPPV infection, and also for further study in the prevention and intervention of this viral disease.

Highlights

  • Ovine progressive pneumonia virus (OPPV), or visna/maedi virus (VMV) in sheep [1,2,3], and caprine arthritis encephalitis virus (CAEV) in goats [4,5,6], all belong to one viral species called small ruminant lentiviruses (SRLV) according to current viral classifications [7]

  • During OPPV infection, the host responds to the infection and launches anti-viral defenses from both the innate and adaptive arms of the immune system

  • Our results indicate that OPPV infection dynamics peak at 12h p.i., and are reduced about one half by 24h p.i., remaining constant until 48h p.i. (Fig 1)

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Summary

Introduction

Ovine progressive pneumonia virus (OPPV), or visna/maedi virus (VMV) in sheep [1,2,3], and caprine arthritis encephalitis virus (CAEV) in goats [4,5,6], all belong to one viral species called small ruminant lentiviruses (SRLV) according to current viral classifications [7]. These viruses are genetically very similar, with some OPPV strains being more closely related to CAEV than to other OPPV strains [7]. Subtype classification of SRLV has been applied based on viral genetic

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