Snapshot of viral infections in wild carnivores reveals ubiquity of parvovirus and susceptibility of Egyptian mongoose to feline panleukopenia virus

PLoS One. 2013;8(3):e59399. doi: 10.1371/journal.pone.0059399. Epub 2013 Mar 20.

Abstract

The exposure of wild carnivores to viral pathogens, with emphasis on parvovirus (CPV/FPLV), was assessed based on the molecular screening of tissue samples from 128 hunted or accidentally road-killed animals collected in Portugal from 2008 to 2011, including Egyptian mongoose (Herpestes ichneumon, n = 99), red fox (Vulpes vulpes, n = 19), stone marten (Martes foina, n = 3), common genet (Genetta genetta, n = 3) and Eurasian badger (Meles meles, n = 4). A high prevalence of parvovirus DNA (63%) was detected among all surveyed species, particularly in mongooses (58%) and red foxes (79%), along with the presence of CPV/FPLV circulating antibodies that were identified in 90% of a subset of parvovirus-DNA positive samples. Most specimens were extensively autolysed, restricting macro and microscopic investigations for lesion evaluation. Whenever possible to examine, signs of active disease were not present, supporting the hypothesis that the parvovirus vp2 gene fragments detected by real-time PCR possibly correspond to viral DNA reminiscent from previous infections. The molecular characterization of viruses, based on the analysis of the complete or partial sequence of the vp2 gene, allowed typifying three viral strains of mongoose and four red fox's as feline panleukopenia virus (FPLV) and one stone marten's as newCPV-2b type. The genetic similarity found between the FPLV viruses from free-ranging and captive wild species originated in Portugal and publicly available comparable sequences, suggests a closer genetic relatedness among FPLV circulating in Portugal. Although the clinical and epidemiological significance of infection could not be established, this study evidences that exposure of sympatric wild carnivores to parvovirus is common and geographically widespread, potentially carrying a risk to susceptible populations at the wildlife-domestic interface and to threatened species, such as the wildcat (Felis silvestris) and the critically endangered Iberian lynx (Lynx pardinus).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animal Distribution*
  • Animals
  • Antibodies, Viral / blood
  • Area Under Curve
  • Base Sequence
  • Bayes Theorem
  • Capsid Proteins / genetics
  • Carnivora / virology*
  • Disease Susceptibility / veterinary*
  • Feline Panleukopenia Virus / genetics*
  • Herpestidae / virology*
  • Models, Genetic
  • Molecular Sequence Data
  • Parvoviridae Infections / epidemiology*
  • Parvoviridae Infections / pathology
  • Phylogeny*
  • Portugal / epidemiology
  • Real-Time Polymerase Chain Reaction / veterinary
  • Sequence Alignment
  • Species Specificity

Substances

  • Antibodies, Viral
  • Capsid Proteins

Grants and funding

The authors are grateful to Fundação para a Ciência e Tecnologia (FCT), Portugal, for funding research contracts to MVC, AMH and SCB, in the framework of “Ciência 2008” Program, a post-doctoral fellowship to LMR (SFRH/BPD/14435/2003), and PhD grants to MPB (SFRH/BD/38410/2007), TB (SFRH/BD/71112/2010), and VB (SFRH/BD/51540/2011). MVC and CF acknowledge FCT through QREN-POFC-COMPETE program (PTDC/CVT/117794/2010 and PTDC/BIA-BEC/104401/2008). LMR also acknowledges the financial support from FAPESP (Proc. 2011/00408-4). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.