Long-term infection passaging of Human Adenovirus 36 in monkey kidney cells
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Revista do Instituto de Medicina Tropical de São Paulo |
Texto Completo: | https://www.revistas.usp.br/rimtsp/article/view/204564 |
Resumo: | Human Adenovirus 36 (HAdV-36) has been related to diverse effects on metabolism and may attenuate the lipid accumulation in kidneys with increased adiposity. Some of these effects would be related to viral persistence. However, until now, a model of persistent in vitro infection by HAdV-36 is unknown. In this study, we examined the cells of the Vero lineage to explore their permissiveness to long-term HAdV-36 infection. HAdV-36 was productively replicated in Vero cells and maintained long-term infection for up to 35 cell passages. A subculture was obtained from the cells that survived the primary infection at a low MOI (0.5). The production of the extracellular infectious virus with titers ranging from 104 to 106 TCID50/mL and DNA-bearing cells was detected. In long-term infected cells, the intracellular distribution of viral antigen was demonstrated by performing immunolocalization (IFI) and expression of cell-viral antigen in 50% of cells by flow cytometry, using anti-HAdV-36 hyperimmune rabbit serum. Furthermore, E1a and E4orf1 genes in long-term infected passages showed a decreasing trend. Our preliminary results reveal that renal epithelial monkey cells are permissive for the productive infection of HAdV-36. Vero cell culture long-term infection might be a promising model for addressing the fundamental aspects of the HAdV-36 biology that cannot reveal broadly-used cultures, which do not maintain long-term infection in primary or transformed cells. |
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Long-term infection passaging of Human Adenovirus 36 in monkey kidney cellsHAdV-36Ad36Vero cellsHAdV-36 long-term in vitro infectionHuman Adenovirus 36 (HAdV-36) has been related to diverse effects on metabolism and may attenuate the lipid accumulation in kidneys with increased adiposity. Some of these effects would be related to viral persistence. However, until now, a model of persistent in vitro infection by HAdV-36 is unknown. In this study, we examined the cells of the Vero lineage to explore their permissiveness to long-term HAdV-36 infection. HAdV-36 was productively replicated in Vero cells and maintained long-term infection for up to 35 cell passages. A subculture was obtained from the cells that survived the primary infection at a low MOI (0.5). The production of the extracellular infectious virus with titers ranging from 104 to 106 TCID50/mL and DNA-bearing cells was detected. In long-term infected cells, the intracellular distribution of viral antigen was demonstrated by performing immunolocalization (IFI) and expression of cell-viral antigen in 50% of cells by flow cytometry, using anti-HAdV-36 hyperimmune rabbit serum. Furthermore, E1a and E4orf1 genes in long-term infected passages showed a decreasing trend. Our preliminary results reveal that renal epithelial monkey cells are permissive for the productive infection of HAdV-36. Vero cell culture long-term infection might be a promising model for addressing the fundamental aspects of the HAdV-36 biology that cannot reveal broadly-used cultures, which do not maintain long-term infection in primary or transformed cells.Universidade de São Paulo. Instituto de Medicina Tropical de São Paulo2022-11-17info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/rimtsp/article/view/20456410.1590/S1678-9946202264068Revista do Instituto de Medicina Tropical de São Paulo; Vol. 64 (2022); e68Revista do Instituto de Medicina Tropical de São Paulo; Vol. 64 (2022); e68Revista do Instituto de Medicina Tropical de São Paulo; v. 64 (2022); e681678-99460036-4665reponame:Revista do Instituto de Medicina Tropical de São Pauloinstname:Instituto de Medicina Tropical (IMT)instacron:IMTenghttps://www.revistas.usp.br/rimtsp/article/view/204564/188154Copyright (c) 2022 Patricia Alarcon-Valdes, Fabiola Sanchez-Aguillon, Fernando Martinez-Hernandez, Angelica Olivo-Diaz, Pablo Maravilla, Jonnathan Guadalupe Santillan-Benitez, Mirza Romero-Valdovinoshttps://creativecommons.org/licenses/by-nc/4.0info:eu-repo/semantics/openAccessAlarcon-Valdes, Patricia Sanchez-Aguillon, Fabiola Martinez-Hernandez, Fernando Olivo-Diaz, Angelica Maravilla, Pablo Santillan-Benitez, Jonnathan Guadalupe Romero-Valdovinos, Mirza 2022-11-17T18:00:44Zoai:revistas.usp.br:article/204564Revistahttp://www.revistas.usp.br/rimtsp/indexPUBhttps://www.revistas.usp.br/rimtsp/oai||revimtsp@usp.br1678-99460036-4665opendoar:2022-12-13T16:54:10.944105Revista do Instituto de Medicina Tropical de São Paulo - Instituto de Medicina Tropical (IMT)true |
dc.title.none.fl_str_mv |
Long-term infection passaging of Human Adenovirus 36 in monkey kidney cells |
title |
Long-term infection passaging of Human Adenovirus 36 in monkey kidney cells |
spellingShingle |
Long-term infection passaging of Human Adenovirus 36 in monkey kidney cells Alarcon-Valdes, Patricia HAdV-36 Ad36 Vero cells HAdV-36 long-term in vitro infection |
title_short |
Long-term infection passaging of Human Adenovirus 36 in monkey kidney cells |
title_full |
Long-term infection passaging of Human Adenovirus 36 in monkey kidney cells |
title_fullStr |
Long-term infection passaging of Human Adenovirus 36 in monkey kidney cells |
title_full_unstemmed |
Long-term infection passaging of Human Adenovirus 36 in monkey kidney cells |
title_sort |
Long-term infection passaging of Human Adenovirus 36 in monkey kidney cells |
author |
Alarcon-Valdes, Patricia |
author_facet |
Alarcon-Valdes, Patricia Sanchez-Aguillon, Fabiola Martinez-Hernandez, Fernando Olivo-Diaz, Angelica Maravilla, Pablo Santillan-Benitez, Jonnathan Guadalupe Romero-Valdovinos, Mirza |
author_role |
author |
author2 |
Sanchez-Aguillon, Fabiola Martinez-Hernandez, Fernando Olivo-Diaz, Angelica Maravilla, Pablo Santillan-Benitez, Jonnathan Guadalupe Romero-Valdovinos, Mirza |
author2_role |
author author author author author author |
dc.contributor.author.fl_str_mv |
Alarcon-Valdes, Patricia Sanchez-Aguillon, Fabiola Martinez-Hernandez, Fernando Olivo-Diaz, Angelica Maravilla, Pablo Santillan-Benitez, Jonnathan Guadalupe Romero-Valdovinos, Mirza |
dc.subject.por.fl_str_mv |
HAdV-36 Ad36 Vero cells HAdV-36 long-term in vitro infection |
topic |
HAdV-36 Ad36 Vero cells HAdV-36 long-term in vitro infection |
description |
Human Adenovirus 36 (HAdV-36) has been related to diverse effects on metabolism and may attenuate the lipid accumulation in kidneys with increased adiposity. Some of these effects would be related to viral persistence. However, until now, a model of persistent in vitro infection by HAdV-36 is unknown. In this study, we examined the cells of the Vero lineage to explore their permissiveness to long-term HAdV-36 infection. HAdV-36 was productively replicated in Vero cells and maintained long-term infection for up to 35 cell passages. A subculture was obtained from the cells that survived the primary infection at a low MOI (0.5). The production of the extracellular infectious virus with titers ranging from 104 to 106 TCID50/mL and DNA-bearing cells was detected. In long-term infected cells, the intracellular distribution of viral antigen was demonstrated by performing immunolocalization (IFI) and expression of cell-viral antigen in 50% of cells by flow cytometry, using anti-HAdV-36 hyperimmune rabbit serum. Furthermore, E1a and E4orf1 genes in long-term infected passages showed a decreasing trend. Our preliminary results reveal that renal epithelial monkey cells are permissive for the productive infection of HAdV-36. Vero cell culture long-term infection might be a promising model for addressing the fundamental aspects of the HAdV-36 biology that cannot reveal broadly-used cultures, which do not maintain long-term infection in primary or transformed cells. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022-11-17 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://www.revistas.usp.br/rimtsp/article/view/204564 10.1590/S1678-9946202264068 |
url |
https://www.revistas.usp.br/rimtsp/article/view/204564 |
identifier_str_mv |
10.1590/S1678-9946202264068 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://www.revistas.usp.br/rimtsp/article/view/204564/188154 |
dc.rights.driver.fl_str_mv |
https://creativecommons.org/licenses/by-nc/4.0 info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc/4.0 |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Universidade de São Paulo. Instituto de Medicina Tropical de São Paulo |
publisher.none.fl_str_mv |
Universidade de São Paulo. Instituto de Medicina Tropical de São Paulo |
dc.source.none.fl_str_mv |
Revista do Instituto de Medicina Tropical de São Paulo; Vol. 64 (2022); e68 Revista do Instituto de Medicina Tropical de São Paulo; Vol. 64 (2022); e68 Revista do Instituto de Medicina Tropical de São Paulo; v. 64 (2022); e68 1678-9946 0036-4665 reponame:Revista do Instituto de Medicina Tropical de São Paulo instname:Instituto de Medicina Tropical (IMT) instacron:IMT |
instname_str |
Instituto de Medicina Tropical (IMT) |
instacron_str |
IMT |
institution |
IMT |
reponame_str |
Revista do Instituto de Medicina Tropical de São Paulo |
collection |
Revista do Instituto de Medicina Tropical de São Paulo |
repository.name.fl_str_mv |
Revista do Instituto de Medicina Tropical de São Paulo - Instituto de Medicina Tropical (IMT) |
repository.mail.fl_str_mv |
||revimtsp@usp.br |
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1798951659406098432 |