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Pleural effusion disease in rabbits: Observations on viraemia, immunity and transmissibility

Baby rabbits surviving infection with pleural effusion disease virus (PEDV) developed viraemia persisting for at least six months. Only the infectious serum samples collected during the first 2 months of disease could transfer the typical PED. Six months after neonatal infection, virus concentration...

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Detalles Bibliográficos
Autores principales: Fennestad, K. L., Mansa, B., Larsen, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 1981
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7086771/
https://www.ncbi.nlm.nih.gov/pubmed/7332487
http://dx.doi.org/10.1007/BF01320789
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author Fennestad, K. L.
Mansa, B.
Larsen, S.
author_facet Fennestad, K. L.
Mansa, B.
Larsen, S.
author_sort Fennestad, K. L.
collection PubMed
description Baby rabbits surviving infection with pleural effusion disease virus (PEDV) developed viraemia persisting for at least six months. Only the infectious serum samples collected during the first 2 months of disease could transfer the typical PED. Six months after neonatal infection, virus concentration in serum was 10(2) to 10(4) rabbit-infectious doses per ml, the level of IgG appeared elevated, and serum rendered non-infectious by ether-treatment had a protective effect in passive immunisation experiments. No evidence of glomerulonephritis or deposits of immunoglobulins could be demonstrated in the kidneys. During the nursing period PEDV was transmitted from infected baby rabbits to two out of four dams, but not to control litter-mates. After the nursing period control rabbits, caged together with the viraemic rabbits for 60 to 150 days, remained free from PEDV infection.
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spelling pubmed-70867712020-03-23 Pleural effusion disease in rabbits: Observations on viraemia, immunity and transmissibility Fennestad, K. L. Mansa, B. Larsen, S. Arch Virol Original Papers Baby rabbits surviving infection with pleural effusion disease virus (PEDV) developed viraemia persisting for at least six months. Only the infectious serum samples collected during the first 2 months of disease could transfer the typical PED. Six months after neonatal infection, virus concentration in serum was 10(2) to 10(4) rabbit-infectious doses per ml, the level of IgG appeared elevated, and serum rendered non-infectious by ether-treatment had a protective effect in passive immunisation experiments. No evidence of glomerulonephritis or deposits of immunoglobulins could be demonstrated in the kidneys. During the nursing period PEDV was transmitted from infected baby rabbits to two out of four dams, but not to control litter-mates. After the nursing period control rabbits, caged together with the viraemic rabbits for 60 to 150 days, remained free from PEDV infection. Springer-Verlag 1981 /pmc/articles/PMC7086771/ /pubmed/7332487 http://dx.doi.org/10.1007/BF01320789 Text en © Springer-Verlag 1981 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Original Papers
Fennestad, K. L.
Mansa, B.
Larsen, S.
Pleural effusion disease in rabbits: Observations on viraemia, immunity and transmissibility
title Pleural effusion disease in rabbits: Observations on viraemia, immunity and transmissibility
title_full Pleural effusion disease in rabbits: Observations on viraemia, immunity and transmissibility
title_fullStr Pleural effusion disease in rabbits: Observations on viraemia, immunity and transmissibility
title_full_unstemmed Pleural effusion disease in rabbits: Observations on viraemia, immunity and transmissibility
title_short Pleural effusion disease in rabbits: Observations on viraemia, immunity and transmissibility
title_sort pleural effusion disease in rabbits: observations on viraemia, immunity and transmissibility
topic Original Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7086771/
https://www.ncbi.nlm.nih.gov/pubmed/7332487
http://dx.doi.org/10.1007/BF01320789
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