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Transplacental transmission of field and rescued strains of BTV-2 and BTV-8 in experimentally infected sheep

Transplacental transmission of bluetongue virus has been shown previously for the North European strain of serotype 8 (BTV-8) and for tissue culture or chicken egg-adapted vaccine strains but not for field strains of other serotypes. In this study, pregnant ewes (6 per group) were inoculated with ei...

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Autores principales: Rasmussen, Lasse Dam, Savini, Giovanni, Lorusso, Alessio, Bellacicco, Anna, Palmarini, Massimo, Caporale, Marco, Rasmussen, Thomas Bruun, Belsham, Graham J, Bøtner, Anette
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3848766/
https://www.ncbi.nlm.nih.gov/pubmed/24007601
http://dx.doi.org/10.1186/1297-9716-44-75
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author Rasmussen, Lasse Dam
Savini, Giovanni
Lorusso, Alessio
Bellacicco, Anna
Palmarini, Massimo
Caporale, Marco
Rasmussen, Thomas Bruun
Belsham, Graham J
Bøtner, Anette
author_facet Rasmussen, Lasse Dam
Savini, Giovanni
Lorusso, Alessio
Bellacicco, Anna
Palmarini, Massimo
Caporale, Marco
Rasmussen, Thomas Bruun
Belsham, Graham J
Bøtner, Anette
author_sort Rasmussen, Lasse Dam
collection PubMed
description Transplacental transmission of bluetongue virus has been shown previously for the North European strain of serotype 8 (BTV-8) and for tissue culture or chicken egg-adapted vaccine strains but not for field strains of other serotypes. In this study, pregnant ewes (6 per group) were inoculated with either field or rescued strains of BTV-2 and BTV-8 in order to determine the ability of these viruses to cross the placental barrier. The field BTV-2 and BTV-8 strains was passaged once in Culicoides KC cells and once in mammalian cells. All virus inoculated sheep became infected and seroconverted against the different BTV strains used in this study. BTV RNA was detectable in the blood of all but two ewes for over 28 days but infectious virus could only be detected in the blood for a much shorter period. Interestingly, transplacental transmission of BTV-2 (both field and rescued strains) was demonstrated at high efficiency (6 out of 13 lambs born to BTV-2 infected ewes) while only 1 lamb of 12 born to BTV-8 infected ewes showed evidence of in utero infection. In addition, evidence for horizontal transmission of BTV-2 between ewes was observed. As expected, the parental BTV-2 and BTV-8 viruses and the viruses rescued by reverse genetics showed very similar properties to each other. This study showed, for the first time, that transplacental transmission of BTV-2, which had been minimally passaged in cell culture, can occur; hence such transmission might be more frequent than previously thought.
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spelling pubmed-38487662013-12-04 Transplacental transmission of field and rescued strains of BTV-2 and BTV-8 in experimentally infected sheep Rasmussen, Lasse Dam Savini, Giovanni Lorusso, Alessio Bellacicco, Anna Palmarini, Massimo Caporale, Marco Rasmussen, Thomas Bruun Belsham, Graham J Bøtner, Anette Vet Res Research Transplacental transmission of bluetongue virus has been shown previously for the North European strain of serotype 8 (BTV-8) and for tissue culture or chicken egg-adapted vaccine strains but not for field strains of other serotypes. In this study, pregnant ewes (6 per group) were inoculated with either field or rescued strains of BTV-2 and BTV-8 in order to determine the ability of these viruses to cross the placental barrier. The field BTV-2 and BTV-8 strains was passaged once in Culicoides KC cells and once in mammalian cells. All virus inoculated sheep became infected and seroconverted against the different BTV strains used in this study. BTV RNA was detectable in the blood of all but two ewes for over 28 days but infectious virus could only be detected in the blood for a much shorter period. Interestingly, transplacental transmission of BTV-2 (both field and rescued strains) was demonstrated at high efficiency (6 out of 13 lambs born to BTV-2 infected ewes) while only 1 lamb of 12 born to BTV-8 infected ewes showed evidence of in utero infection. In addition, evidence for horizontal transmission of BTV-2 between ewes was observed. As expected, the parental BTV-2 and BTV-8 viruses and the viruses rescued by reverse genetics showed very similar properties to each other. This study showed, for the first time, that transplacental transmission of BTV-2, which had been minimally passaged in cell culture, can occur; hence such transmission might be more frequent than previously thought. BioMed Central 2013 2013-09-05 /pmc/articles/PMC3848766/ /pubmed/24007601 http://dx.doi.org/10.1186/1297-9716-44-75 Text en Copyright © 2013 Rasmussen et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Rasmussen, Lasse Dam
Savini, Giovanni
Lorusso, Alessio
Bellacicco, Anna
Palmarini, Massimo
Caporale, Marco
Rasmussen, Thomas Bruun
Belsham, Graham J
Bøtner, Anette
Transplacental transmission of field and rescued strains of BTV-2 and BTV-8 in experimentally infected sheep
title Transplacental transmission of field and rescued strains of BTV-2 and BTV-8 in experimentally infected sheep
title_full Transplacental transmission of field and rescued strains of BTV-2 and BTV-8 in experimentally infected sheep
title_fullStr Transplacental transmission of field and rescued strains of BTV-2 and BTV-8 in experimentally infected sheep
title_full_unstemmed Transplacental transmission of field and rescued strains of BTV-2 and BTV-8 in experimentally infected sheep
title_short Transplacental transmission of field and rescued strains of BTV-2 and BTV-8 in experimentally infected sheep
title_sort transplacental transmission of field and rescued strains of btv-2 and btv-8 in experimentally infected sheep
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3848766/
https://www.ncbi.nlm.nih.gov/pubmed/24007601
http://dx.doi.org/10.1186/1297-9716-44-75
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