Long-term infection passaging of Human Adenovirus 36 in monkey kidney cells

Detalhes bibliográficos
Autor(a) principal: Alarcon-Valdes, Patricia
Data de Publicação: 2022
Outros Autores: Sanchez-Aguillon, Fabiola, Martinez-Hernandez, Fernando, Olivo-Diaz, Angelica, Maravilla, Pablo, Santillan-Benitez, Jonnathan Guadalupe, Romero-Valdovinos, Mirza
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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spelling 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)
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