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

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

Author information

1
National Food Chain Safety Office Veterinary Diagnostic Directorate, Budapest, Hungary.
2
National Food Chain Safety Office Directorate of Veterinary Medicinal Products, Budapest, Hungary.
3
Institute for Veterinary Medical Research, Centre for Agricultural Research, Hungarian Academy of Sciences, Budapest, Hungary.
4
Department of Virology, Immunobiology and Parasitology, National Veterinary Institute, SVA, Uppsala, Sweden.

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.

PMID:
24586385
PMCID:
PMC3930587
DOI:
10.1371/journal.pone.0088758
[Indexed for MEDLINE]
Free PMC Article

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