Comparative in vivo analysis of recombinant type II feline coronaviruses with truncated and completed ORF3 region

PLoS One. 2014 Feb 20;9(2):e88758. doi: 10.1371/journal.pone.0088758. eCollection 2014.

Abstract

Our previous in vitro comparative study on a feline coronavirus (FCoV) pair, differing only in the intactness of their ORF3abc regions, showed that the truncated ORF3abc plays an important role in the efficient macrophage/monocyte tropism of type II feline infectious peritonitis virus (FIPV). In the present study, we describe a challenge experiment with the same recombinant FCoVs in order to gain data on the in vivo characteristics on these viruses. While parent virus FIPV DF-2 developed feline infectious peritonitis in all the infected cats, its recombinant virus PBFIPV-DF-2, differing only in seven nucleotides, proved to be surprisingly low virulent, although caused an acute febrile episode similarly to the original FIPV DF-2. PBFIPV-DF-2 infection induced significantly lower virus neutralization titers than its parent virus, and lacked the second phase of viremia and development of fatal course of the disease. The recombinant PBFIPV-DF-2-R3i with completed ORF3abc gained biological properties that differentiate between the feline enteric coronavirus (FECV) and FIPV biotypes such as intensive replication in the gut, absence of viremia and weak or no serological response. Using reverse genetic approaches our study is the first experimental proof that ORF3abc is indeed responsible for the restriction of FECV replication to the intestine in vivo.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Neutralizing / immunology
  • Base Sequence
  • Cat Diseases / virology*
  • Cats
  • Coronavirus, Feline / genetics*
  • Coronavirus, Feline / pathogenicity
  • Enzyme-Linked Immunosorbent Assay / veterinary
  • Feline Infectious Peritonitis / immunology
  • Feline Infectious Peritonitis / virology*
  • Intestines / virology
  • Molecular Sequence Data
  • Open Reading Frames / genetics*
  • Reverse Genetics / methods
  • Sequence Alignment
  • Sequence Analysis, DNA / veterinary
  • Viral Load
  • Virulence
  • Virus Replication / physiology*

Substances

  • Antibodies, Neutralizing

Grants and funding

This study was supported by Award of Excellence from the Swedish University of Agricultural Sciences; Agria Animal Insurance Company Agria Djurförsäkring; Országos Tudományos Kutatási Alapprogramok (OTKA), and Nemzeti Kutatási és Technológiai Hivatal (NKTH) (Mobilitás 08-C OTKA 81187; and János Bolyai Fellowship from the Hungarian Academy of Sciences (BO/00414/10). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.