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Yellow Fever 17DD Vaccine Virus Infection Causes Detectable Changes in Chicken Embryos
The yellow fever (YF) 17D vaccine is one of the most effective human vaccines ever created. The YF vaccine has been produced since 1937 in embryonated chicken eggs inoculated with the YF 17D virus. Yet, little information is available about the infection mechanism of YF 17DD virus in this biological...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4570825/ https://www.ncbi.nlm.nih.gov/pubmed/26371874 http://dx.doi.org/10.1371/journal.pntd.0004064 |
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author | Manso, Pedro Paulo de Abreu Dias de Oliveira, Barbara C. E. P. de Sequeira, Patrícia Carvalho Maia de Souza, Yuli Rodrigues Ferro, Jessica Maria dos Santos da Silva, Igor José Caputo, Luzia Fátima Gonçalves Guedes, Priscila Tavares dos Santos, Alexandre Araujo Cunha Freire, Marcos da Silva Bonaldo, Myrna Cristina Pelajo-Machado, Marcelo |
author_facet | Manso, Pedro Paulo de Abreu Dias de Oliveira, Barbara C. E. P. de Sequeira, Patrícia Carvalho Maia de Souza, Yuli Rodrigues Ferro, Jessica Maria dos Santos da Silva, Igor José Caputo, Luzia Fátima Gonçalves Guedes, Priscila Tavares dos Santos, Alexandre Araujo Cunha Freire, Marcos da Silva Bonaldo, Myrna Cristina Pelajo-Machado, Marcelo |
author_sort | Manso, Pedro Paulo de Abreu |
collection | PubMed |
description | The yellow fever (YF) 17D vaccine is one of the most effective human vaccines ever created. The YF vaccine has been produced since 1937 in embryonated chicken eggs inoculated with the YF 17D virus. Yet, little information is available about the infection mechanism of YF 17DD virus in this biological model. To better understand this mechanism, we infected embryos of Gallus gallus domesticus and analyzed their histopathology after 72 hours of YF infection. Some embryos showed few apoptotic bodies in infected tissues, suggesting mild focal infection processes. Confocal and super-resolution microscopic analysis allowed us to identify as targets of viral infection: skeletal muscle cells, cardiomyocytes, nervous system cells, renal tubular epithelium, lung parenchyma, and fibroblasts associated with connective tissue in the perichondrium and dermis. The virus replication was heaviest in muscle tissues. In all of these specimens, RT-PCR methods confirmed the presence of replicative intermediate and genomic YF RNA. This clearer characterization of cell targets in chicken embryos paves the way for future development of a new YF vaccine based on a new cell culture system. |
format | Online Article Text |
id | pubmed-4570825 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-45708252015-09-18 Yellow Fever 17DD Vaccine Virus Infection Causes Detectable Changes in Chicken Embryos Manso, Pedro Paulo de Abreu Dias de Oliveira, Barbara C. E. P. de Sequeira, Patrícia Carvalho Maia de Souza, Yuli Rodrigues Ferro, Jessica Maria dos Santos da Silva, Igor José Caputo, Luzia Fátima Gonçalves Guedes, Priscila Tavares dos Santos, Alexandre Araujo Cunha Freire, Marcos da Silva Bonaldo, Myrna Cristina Pelajo-Machado, Marcelo PLoS Negl Trop Dis Research Article The yellow fever (YF) 17D vaccine is one of the most effective human vaccines ever created. The YF vaccine has been produced since 1937 in embryonated chicken eggs inoculated with the YF 17D virus. Yet, little information is available about the infection mechanism of YF 17DD virus in this biological model. To better understand this mechanism, we infected embryos of Gallus gallus domesticus and analyzed their histopathology after 72 hours of YF infection. Some embryos showed few apoptotic bodies in infected tissues, suggesting mild focal infection processes. Confocal and super-resolution microscopic analysis allowed us to identify as targets of viral infection: skeletal muscle cells, cardiomyocytes, nervous system cells, renal tubular epithelium, lung parenchyma, and fibroblasts associated with connective tissue in the perichondrium and dermis. The virus replication was heaviest in muscle tissues. In all of these specimens, RT-PCR methods confirmed the presence of replicative intermediate and genomic YF RNA. This clearer characterization of cell targets in chicken embryos paves the way for future development of a new YF vaccine based on a new cell culture system. Public Library of Science 2015-09-15 /pmc/articles/PMC4570825/ /pubmed/26371874 http://dx.doi.org/10.1371/journal.pntd.0004064 Text en © 2015 Manso et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Manso, Pedro Paulo de Abreu Dias de Oliveira, Barbara C. E. P. de Sequeira, Patrícia Carvalho Maia de Souza, Yuli Rodrigues Ferro, Jessica Maria dos Santos da Silva, Igor José Caputo, Luzia Fátima Gonçalves Guedes, Priscila Tavares dos Santos, Alexandre Araujo Cunha Freire, Marcos da Silva Bonaldo, Myrna Cristina Pelajo-Machado, Marcelo Yellow Fever 17DD Vaccine Virus Infection Causes Detectable Changes in Chicken Embryos |
title | Yellow Fever 17DD Vaccine Virus Infection Causes Detectable Changes in Chicken Embryos |
title_full | Yellow Fever 17DD Vaccine Virus Infection Causes Detectable Changes in Chicken Embryos |
title_fullStr | Yellow Fever 17DD Vaccine Virus Infection Causes Detectable Changes in Chicken Embryos |
title_full_unstemmed | Yellow Fever 17DD Vaccine Virus Infection Causes Detectable Changes in Chicken Embryos |
title_short | Yellow Fever 17DD Vaccine Virus Infection Causes Detectable Changes in Chicken Embryos |
title_sort | yellow fever 17dd vaccine virus infection causes detectable changes in chicken embryos |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4570825/ https://www.ncbi.nlm.nih.gov/pubmed/26371874 http://dx.doi.org/10.1371/journal.pntd.0004064 |
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