Abstract

Feline panleukopenia is a common contagious disease with high morbidity and mortality. At present, feline parvovirus (FPV) and canine parvovirus (CPV) variants are the pathogens of feline panleukopenia. Many studies have shown that miRNAs are involved in virus-host interactions. Nevertheless, miRNA expression profiling of FPV (original virus) or CPV-2b (new virus) in cats has not been reported. To investigate these profiles, three 10-week-old cats were orally inoculated with 106 TCID50 of the viruses (FPV and CPV-2b), and the jejunums of one cat in each group were sectioned for miRNA sequencing at 5 days post-inoculation (dpi). This study is the first attempt to use miRNA analysis to understand the molecular basis of FPV and CPV infection in cats. The miRNA expression profiles of the jejunums of cats infected with FPV and CPV were obtained, and a subset of miRNAs was validated by real-time qPCR. The results show that a variety of metabolism-related pathways, cytokine- and pathogen-host interaction-related pathways, and pathology- and cellar structure-related pathways, as well as others, were affected. Specifically, the JAK-STAT signaling pathway, which is critical for cytokines and growth factors, was enriched. This description of the miRNAs involved in regulating FPV and CPV infection in vivo provides further insight into the mechanisms of viral infection and adaptation and might provide an alternative antiviral strategy for disease control and prevention.

Highlights

  • Feline panleukopenia, a common contagious disease with high morbidity and mortality, is caused by the single-stranded DNA virus feline parvovirus (FPV)

  • In addition to the one euthanized cat in each group, the other two FPV-inoculated cats died at 7 dpi and 9 dpi, and the other two Canine parvovirus (CPV)-inoculated cats died at 10 dpi and 11 dpi

  • All inoculated cats persistently shed the virus from 2 dpi until death, and viral titers were persistently near 7.0 logTCID50/ml in the FPV group and near 5.0 logTCID50/ml in the CPV group (Fig 1A)

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Summary

Introduction

A common contagious disease with high morbidity and mortality, is caused by the single-stranded DNA virus feline parvovirus (FPV). FPV is a member of the genus Protoparvovirus in the family Parvoviridae. The DNA genome of FPV is 5.2 kb long and contains two open reading frames (ORFs). The first ORF encodes two non-structural proteins, NS1 and NS2, and the second ORF encodes two structural proteins, VP1 and VP2 [1]. Canine parvovirus (CPV) derived from FPV with several amino acid mutations [2,3,4,5,6], but other evidence suggests that CPV and FPV might have evolved separately from common viral ancestors.

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