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Goat umbilical cord cells are permissive to small ruminant lentivirus infection in vitro
Small ruminant lentiviruses isolated from peripheral blood leukocytes and target organs can be propagated in vitro in fibroblasts derived from goat synovial membrane cells. These cells are obtained from tissues collected from embryos or fetuses and are necessary for the establishment of the fibrobla...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5221357/ https://www.ncbi.nlm.nih.gov/pubmed/27899238 http://dx.doi.org/10.1016/j.bjm.2016.11.002 |
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author | Martins, Gabrielle R. Marinho, Rebeca C. Junior, Rosivaldo Q. Bezerra Alves, Antoniel de O. Câmara, Lilia M.C. Albuquerque-Pinto, Luiz C. Teixeira, Maria F. da S. |
author_facet | Martins, Gabrielle R. Marinho, Rebeca C. Junior, Rosivaldo Q. Bezerra Alves, Antoniel de O. Câmara, Lilia M.C. Albuquerque-Pinto, Luiz C. Teixeira, Maria F. da S. |
author_sort | Martins, Gabrielle R. |
collection | PubMed |
description | Small ruminant lentiviruses isolated from peripheral blood leukocytes and target organs can be propagated in vitro in fibroblasts derived from goat synovial membrane cells. These cells are obtained from tissues collected from embryos or fetuses and are necessary for the establishment of the fibroblast primary culture. A new alternative type of host cells, derived from goat umbilical cord, was isolated and characterized phenotypically with its main purpose being to obtain cell monolayers that could be used for the diagnosis and isolation of small ruminant lentiviruses in cell culture. To accomplish this goal, cells were isolated from umbilical cords; characterized phenotypically by flow cytometry analysis; differentiate into osteogenic, chondrogenic and adipogenic lineage; and submitted to viral challenge. The proliferation of goat umbilical cord cells was fast and cell monolayers formed after 15 days. These cells exhibited morphology, immunophenotype, growth characteristics, and lineage differentiation potential similar to mesenchymal stem cells of other origins. The goat umbilical cord derived cells stained positive for vimentin and CD90, but negative for cytokeratin, CD34 and CD105 markers. Syncytia and cell lysis were observed in cell monolayers infected by CAEV-Cork and MVV-K1514, showing that the cells are permissive to small ruminant lentivirus infection in vitro. These data demonstrate the proliferative competence of cells derived from goat umbilical cords and provide a sound basis for future research to standardize this cell lineage. |
format | Online Article Text |
id | pubmed-5221357 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-52213572017-01-18 Goat umbilical cord cells are permissive to small ruminant lentivirus infection in vitro Martins, Gabrielle R. Marinho, Rebeca C. Junior, Rosivaldo Q. Bezerra Alves, Antoniel de O. Câmara, Lilia M.C. Albuquerque-Pinto, Luiz C. Teixeira, Maria F. da S. Braz J Microbiol Veterinary Microbiology Small ruminant lentiviruses isolated from peripheral blood leukocytes and target organs can be propagated in vitro in fibroblasts derived from goat synovial membrane cells. These cells are obtained from tissues collected from embryos or fetuses and are necessary for the establishment of the fibroblast primary culture. A new alternative type of host cells, derived from goat umbilical cord, was isolated and characterized phenotypically with its main purpose being to obtain cell monolayers that could be used for the diagnosis and isolation of small ruminant lentiviruses in cell culture. To accomplish this goal, cells were isolated from umbilical cords; characterized phenotypically by flow cytometry analysis; differentiate into osteogenic, chondrogenic and adipogenic lineage; and submitted to viral challenge. The proliferation of goat umbilical cord cells was fast and cell monolayers formed after 15 days. These cells exhibited morphology, immunophenotype, growth characteristics, and lineage differentiation potential similar to mesenchymal stem cells of other origins. The goat umbilical cord derived cells stained positive for vimentin and CD90, but negative for cytokeratin, CD34 and CD105 markers. Syncytia and cell lysis were observed in cell monolayers infected by CAEV-Cork and MVV-K1514, showing that the cells are permissive to small ruminant lentivirus infection in vitro. These data demonstrate the proliferative competence of cells derived from goat umbilical cords and provide a sound basis for future research to standardize this cell lineage. Elsevier 2016-11-19 /pmc/articles/PMC5221357/ /pubmed/27899238 http://dx.doi.org/10.1016/j.bjm.2016.11.002 Text en © 2016 Sociedade Brasileira de Microbiologia. Published by Elsevier Editora Ltda. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Veterinary Microbiology Martins, Gabrielle R. Marinho, Rebeca C. Junior, Rosivaldo Q. Bezerra Alves, Antoniel de O. Câmara, Lilia M.C. Albuquerque-Pinto, Luiz C. Teixeira, Maria F. da S. Goat umbilical cord cells are permissive to small ruminant lentivirus infection in vitro |
title | Goat umbilical cord cells are permissive to small ruminant lentivirus infection in vitro |
title_full | Goat umbilical cord cells are permissive to small ruminant lentivirus infection in vitro |
title_fullStr | Goat umbilical cord cells are permissive to small ruminant lentivirus infection in vitro |
title_full_unstemmed | Goat umbilical cord cells are permissive to small ruminant lentivirus infection in vitro |
title_short | Goat umbilical cord cells are permissive to small ruminant lentivirus infection in vitro |
title_sort | goat umbilical cord cells are permissive to small ruminant lentivirus infection in vitro |
topic | Veterinary Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5221357/ https://www.ncbi.nlm.nih.gov/pubmed/27899238 http://dx.doi.org/10.1016/j.bjm.2016.11.002 |
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