Abstract

Porcine circovirus 2 (PCV2) is a single stranded DNA virus with one of the highest mutation rates among DNA viruses. This ability allows it to generate a cloud of mutants constantly providing new opportunities to adapt and evade the immune system. This pig pathogen is associated to many diseases, globally called porcine circovirus diseases (PCVD) and has been a threat to pig industry since its discovery in the early 90’s. Although 11 ORFs have been predicted from its genome, only two main proteins have been deeply characterized, i.e. Rep and Cap. The structural Cap protein possesses the majority of the epitopic determinants of this non-enveloped virus. The evolution of PCV2 is affected by both natural and vaccine-induced immune responses, which enhances the genetic variability, especially in the most immunogenic Cap region. Intra-host variability has been also demonstrated in infected animals where long-lasting infections can take place. However, the association between this intra-host variability and pathogenesis has never been studied for this virus. Here, the within-host PCV2 variability was monitored over time by next generation sequencing during an experimental infection, demonstrating the presence of large heterogeneity. Remarkably, the level of quasispecies diversity, affecting particularly the Cap coding region, was statistically different depending on viremia levels and clinical signs detected after infection. Moreover, we proved the existence of hyper mutant subjects harboring a remarkably higher number of genetic variants. Altogether, these results suggest an interaction between genetic diversity, host immune system and disease severity.

Highlights

  • The viral life-cycle is essentially dominated by a complex balance of interaction and competition with the host

  • These animals were selected based on two main variables: Porcine circovirus 2 (PCV2) viremia measured by real-time quantitative ­PCR23 and fulfillment or not of the diagnostic criteria for PCV2-SD9

  • Animals that did not accomplish the abovementioned definition were considered as non-PCV2-systemic disease (PCV2-SD)

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Summary

Introduction

The viral life-cycle is essentially dominated by a complex balance of interaction and competition with the host. The other ORFs (ORFs 3 to 6) coding for non-structural proteins not essential for viral replication, are involved in regulating cell apoptosis and interacting with the transcription and function of other viral/host proteins, potentially enhancing viral replication, survival, and even immune ­evasion[11,12,13,14]. PCV2 interaction with the host immune system is complex, since both immune activation and suppression have been proven to enhance viral replication, correlating with the emergence of overt clinical s­ igns[17,18]. In the present study, the within-host PCV2 variability was monitored over time by generation sequencing (NGS) in experimentally infected animals showing different clinical outcomes and viral loads

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