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Journal of Virology, April 2007, p. 3327-3338, Vol. 81, No. 7
0022-538X/07/$08.00+0     doi:10.1128/JVI.02372-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Bovine Viral Diarrhea Virus: Prevention of Persistent Fetal Infection by a Combination of Two Mutations Affecting Erns RNase and Npro Protease{triangledown}

Gregor Meyers,1* Andreas Ege,1 Christiane Fetzer,1,{dagger} Martina von Freyburg,1,{ddagger} Knut Elbers,2 Veronica Carr,3 Helen Prentice,3 Bryan Charleston,3 and Eva-Maria Schürmann1

Institut für Immunologie, Friedrich-Loeffler-Institut, D-72001 Tübingen, Germany,1 Boehringer Ingelheim Vetmedica GmbH, D-55216 Ingelheim am Rhein, Germany,2 Institute for Animal Health, Compton, Newbury, Berkshire RG20 7NN, United Kingdom3

Received 30 October 2006/ Accepted 3 January 2007

Different genetically engineered mutants of bovine viral diarrhea virus (BVDV) were analyzed for the ability to establish infection in the fetuses of pregnant heifers. The virus mutants exhibited either a deletion of the overwhelming part of the genomic region coding for the N-terminal protease Npro, a deletion of codon 349, which abrogates the RNase activity of the structural glycoprotein Erns, or a combination of both mutations. Two months after infection of pregnant cattle with wild-type virus or either of the single mutants, the majority of the fetuses contained virus or were aborted or found dead in the uterus. In contrast, the double mutant was not recovered from fetal tissues after a similar challenge, and no dead fetuses were found. This result was verified with a nonrelated BVDV containing similar mutations. After intrauterine challenge with wild-type virus, mutated viruses, and cytopathogenic BVDV, all viruses could be detected in fetal tissue after 5, 7, and 14 days. Type 1 interferon (IFN) could be detected in fetal serum after challenge, except with wild-type noncytopathogenic BVDV. On days 7 and 14 after challenge, the largest quantities of IFN in fetal serum were induced by the Npro and RNase-negative double mutant virus. The longer duration of fetal infection with the double mutant resulted in abortion. Therefore, for the first time, we have demonstrated the essential role of both Npro and Erns RNase in blocking interferon induction and establishing persistent infection by a pestivirus in the natural host.

* Corresponding author. Mailing address: Institut für Immunologie, Friedrich-Loeffler-Institut, Paul-Ehrlich-Str. 28, D-72076 Tübingen, Germany. Phone: 49 7071-9670. Fax: 49 7071-967303. E-mail: gregor.meyers{at}fli.bund.de.

{triangledown} Published ahead of print on 10 January 2007.

{dagger} Present address: BioScreen European Veterinary Disease Management Center GmbH, Mendelstr. 11, Building L1, D-48149 Münster, Germany.

{ddagger} Present address: Boehringer Ingelheim Vetmedica GmbH, D-55216 Ingelheim am Rhein, Germany.

Journal of Virology, April 2007, p. 3327-3338, Vol. 81, No. 7
0022-538X/07/$08.00+0     doi:10.1128/JVI.02372-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.



This article has been cited by other articles:

  • Tews, B. A., Schurmann, E.-M., Meyers, G. (2009). Mutation of Cysteine 171 of Pestivirus Erns RNase Prevents Homodimer Formation and Leads to Attenuation of Classical Swine Fever Virus. J. Virol. 83: 4823-4834 [Abstract] [Full Text]  
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