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Kinetic Study of Yellow Fever 17DD Viral Infection in Gallus gallus domesticus Embryos

Yellow fever continues to be an important epidemiological problem in Africa and South America even though the disease can be controlled by vaccination. The vaccine has been produced since 1937 and is based on YFV 17DD chicken embryo infection. However, little is known about the histopathological bac...

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Detalles Bibliográficos
Autores principales: Manso, Pedro Paulo de Abreu, E. P. Dias de Oliveira, Bárbara Cristina, Carvalho de Sequeira, Patrícia, Rodrigues Maia de Souza, Yuli, dos Santos Ferro, Jessica Maria, da Silva, Igor José, Gonçalves Caputo, Luzia Fátima, Tavares Guedes, Priscila, Araujo Cunha dos Santos, Alexandre, da Silva Freire, Marcos, Bonaldo, Myrna Cristina, Pelajo Machado, Marcelo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4861264/
https://www.ncbi.nlm.nih.gov/pubmed/27158977
http://dx.doi.org/10.1371/journal.pone.0155041
Descripción
Sumario:Yellow fever continues to be an important epidemiological problem in Africa and South America even though the disease can be controlled by vaccination. The vaccine has been produced since 1937 and is based on YFV 17DD chicken embryo infection. However, little is known about the histopathological background of virus infection and replication in this model. Here we show by morphological and molecular methods (brightfield and confocal microscopies, immunofluorescence, nested-PCR and sequencing) the kinetics of YFV 17DD infection in chicken embryos with 9 days of development, encompassing 24 to 96 hours post infection. Our principal findings indicate that the main cells involved in virus production are myoblasts with a mesenchymal shape, which also are the first cells to express virus proteins in Gallus gallus embryos at 48 hours after infection. At 72 hours post infection, we observed an increase of infected cells in embryos. Many sites are thus affected in the infection sequence, especially the skeletal muscle. We were also able to confirm an increase of nervous system infection at 96 hours post infection. Our data contribute to the comprehension of the pathogenesis of YF 17DD virus infection in Gallus gallus embryos.