Replication of cytopathic and noncytopathic bovine viral diarrhea virus in zona-free and zona-intact in vitro-produced bovine embryos and the effect on embryo quality

Biol Reprod. 1998 Mar;58(3):857-66. doi: 10.1095/biolreprod58.3.857.

Abstract

The aim of the present study was to determine whether or not cytopathic (CP) and noncytopathic (NCP) bovine viral diarrhea virus (BVDV) are able to replicate within in vitro-produced embryos and to investigate whether inoculation of embryos with BVDV affects their normal development. Zona pellucida (ZP)-free oocytes, zygotes, 8-cell-stage embryos, morulae, and hatched blastocysts (HB) were incubated for 1 h in 1 ml of Minimal Essential Medium containing 10(6.00) tissue culture infectious dose (TCID)50/ml NCP BVDV isolate 22,146 or 10(6.25) TCID50/ml CP BVDV strain Oregon C24V. At 0, 12, 24, 36, 48, 60, and 72 h postinoculation (hpi), groups of embryos were collected for virus titration. A small amount of newly produced virus was detected in 8-cell embryos at 60 hpi (10(1.8) TCID50/100 cells), but only for CP BVDV. For ZP-free morulae and HB, maximal intracellular virus titers were, respectively, 10(1.47) and 10(2.33) TCID50/100 cells at 48 hpi for the CP biotype and 10(0.64) and 10(0.84) TCID50/100 cells at 72 hpi for the NCP biotype. Only an infection with CP BVDV had a significant inhibitory effect on further development of ZP-free morulae. It can be concluded that ZP-free in vitro-produced embryos are permissive to an infection with BVDV, with increasing susceptibility of the embryos in accordance with their developmental stage. In contrast to observations in ZP-free in vitro-produced embryos, no virus replication or signs of embryonic degeneration were detected in ZP-intact in vitro-derived embryos.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Viral / metabolism
  • Blastocyst / cytology
  • Blastocyst / virology
  • Bovine Virus Diarrhea-Mucosal Disease / prevention & control
  • Bovine Virus Diarrhea-Mucosal Disease / transmission
  • Bovine Virus Diarrhea-Mucosal Disease / virology
  • Cattle
  • Cytopathogenic Effect, Viral
  • Diarrhea Viruses, Bovine Viral / immunology
  • Diarrhea Viruses, Bovine Viral / pathogenicity*
  • Diarrhea Viruses, Bovine Viral / physiology*
  • Embryo Transfer / adverse effects
  • Embryo Transfer / veterinary
  • Embryo, Mammalian / virology*
  • Embryonic and Fetal Development
  • Fertilization in Vitro
  • In Vitro Techniques
  • Virus Replication*
  • Zona Pellucida / physiology

Substances

  • Antigens, Viral