Abstract

Canine minute virus (CnMV) is a member of the Bocavirus genus, together with Bovine parvovirus (BPV), which emerged as a new pathogen of dogs in 1967. The genus Bocavirus gained more recognition after the recent identification of Human bocavirus in pooled specimens from the respiratory tract of children. The cell culture host range of CnMV appears to be restricted to the Walter Reed canine cell (WRCC) line, although there is a report that indicates susceptibility of the Madin-Darby canine kidney (MDCK) cell line. In order to study the susceptibility of different cell lines to CnMV, the replication in cell cultures of canine, bovine, and human origin and the interaction of the virus with freshly isolated canine peripheral blood mononuclear cells were evaluated. The in vitro host range was unexpectedly wide. As shown by indirect fluorescent antibody and polymerase chain reaction assays, CnMV replicates efficiently in the A72 and MDCK canine cell lines. Bovine and human cell lines support the replication of CnMV less efficiently. In contrast, canine mononuclear blood cells are permissive to replication of CnMV in vitro. The present study revealed the ability of CnMV to replicate in continuous cell lines of different origin and, partially, in canine mononuclear cells.

Highlights

  • Canine minute virus (CnMV) and Bovine parvovirus (BPV) are members of the genus Bocavirus within the Parvoviridae family

  • A virus associated with lower respiratory tract infections in human beings was identified in 2005 and named Human bocavirus (HBoV) because of its similarity to BPV and CnMV

  • The Walter Reed canine cell (WRCC) line has been reported to support the growth of CnMV.[2]

Read more

Summary

Introduction

Canine minute virus (CnMV) and Bovine parvovirus (BPV) are members of the genus Bocavirus within the Parvoviridae family. In order to study the susceptibility of cell cultures to infection with CnMV, the replication of CnMV in different cell lines of canine, bovine, and human origin was tested.

Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.