Literature DB >> 24239972

The DNA replication, virogenesis and infection of canine minute virus in non-permissive and permissive cells.

Fang Li1, Qian Zhang2, Qing Yao2, Long Chen2, Jianning Li2, Jianming Qiu3, Yuning Sun4.   

Abstract

Canine minute virus (CnMV), a kind of autonomous parvovirus, is a member of genus bocavirus in parvovirdae family. In our previous study, we constructed and obtained infectious clones of CnMV, analyzed genome characteristics, RNA transcription profile, and revealed some molecular mechanisms of cytopathic effect of target cells. The purpose of this study was to investigate DNA replication, virogenesis and infectious tropism of CnMV in non-permissive and permissive cells. We demonstrated that the genomic DNA of CnMV, besides WRD cells, could replicate significantly in some non-permissive cells (CrFK, EBtR and COS-7) following transfection with infectious clone of CnMV, pI-MVC. Moreover, by using Western blotting and immunofluorescence, we found that the NS1 protein of CnMV was obviously expressed in both 293, CrFK, EBtR and COS-7 cells transfected with pI-MVC. Meanwhile, two-rounds of reinfection on WRD cells (blind passage) of the transfected cell lysates in CrFK, EBtR and COS-7 cells tranfected with pI-MVC showed that pI-MVC could produce infectious virions in these types of non-permissive cells. Furthermore, it is confirmed that CnMV only infected WRD cells (permissive cells for CnMV), could not infect any non-permissive cells including CrFK, EBtR, COS-7, HK293, A549 and A9 cells. Taken together, for the first time, we have demonstrated that bocavirus CnMV DNA could replicate and form infectious progeny virus in some non-permissive cells. And what is more, unlike other parvoviruses, CnMV did not infect some non-permissive cells, although the DNA replication of CnMV occurred in these cells.
Copyright © 2013 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Bocavirus; Canine minute virus; DNA replication; Infection; Non-permissive cells; Permissive cells; Virogenesis

Mesh:

Year:  2013        PMID: 24239972     DOI: 10.1016/j.virusres.2013.10.019

Source DB:  PubMed          Journal:  Virus Res        ISSN: 0168-1702            Impact factor:   3.303


  1 in total

1.  Classic nuclear localization signals and a novel nuclear localization motif are required for nuclear transport of porcine parvovirus capsid proteins.

Authors:  Maude Boisvert; Véronique Bouchard-Lévesque; Sandra Fernandes; Peter Tijssen
Journal:  J Virol       Date:  2014-07-30       Impact factor: 5.103

  1 in total

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