Iron and glucose-regulated protein 78: fundamental components in the coinfection of Rhizopus oryzae and SARS-CoV-2
Autor(a) principal: | |
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Data de Publicação: | 2023 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | por |
Título da fonte: | Clinical and Biomedical Research |
Texto Completo: | https://seer.ufrgs.br/index.php/hcpa/article/view/122904 |
Resumo: | The viral outbreak of severe acute respiratory syndrome coronavirus 2 emerged in China by the end of 2019 and was declared a global pandemic in early 2020. Along with the growing number of fatalities and lack of specific treatment at the time, the increasing incidence of mucormycosis worried World health agencies, as it ran the risk of more threatening outcomes for COVID-19 patients. In this context, this review aims to assemble case reports of COVID-19 associated mucormycosis and discuss virulence and host factors involved in the progress of these infections – key aspects that might unveil biological targets and pharmacological approaches to treat these infections. Recently, elevated serum iron levels during SARS-CoV-2 infection have been reported in the literature. Besides being a clinical characteristic of diabetic patients, iron overload is described as a risk factor for Rhizopus oryzae infection. Furthermore, the increased expression of human heat-shock protein GRP78 during iron overload and coronavirus infection displays a crucial role as a mediator in Mucorales invasion. These remarkable mechanisms might explain the high incidence of mucormycosis in COVID-19 patients with diabetes and, therefore, suggest regulation of GRP78 expression, management of glycemia and glucocorticoid treatment as potential therapeutic targets of this severe coinfection. |
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Clinical and Biomedical Research |
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Iron and glucose-regulated protein 78: fundamental components in the coinfection of Rhizopus oryzae and SARS-CoV-2Iron and glucose-regulated protein 78: fundamental components in the coinfection of Rhizopus oryzae and SARS-CoV-2SARS-CoV-2 InfectionsCOVID-19IronGRP78MucormycosisThe viral outbreak of severe acute respiratory syndrome coronavirus 2 emerged in China by the end of 2019 and was declared a global pandemic in early 2020. Along with the growing number of fatalities and lack of specific treatment at the time, the increasing incidence of mucormycosis worried World health agencies, as it ran the risk of more threatening outcomes for COVID-19 patients. In this context, this review aims to assemble case reports of COVID-19 associated mucormycosis and discuss virulence and host factors involved in the progress of these infections – key aspects that might unveil biological targets and pharmacological approaches to treat these infections. Recently, elevated serum iron levels during SARS-CoV-2 infection have been reported in the literature. Besides being a clinical characteristic of diabetic patients, iron overload is described as a risk factor for Rhizopus oryzae infection. Furthermore, the increased expression of human heat-shock protein GRP78 during iron overload and coronavirus infection displays a crucial role as a mediator in Mucorales invasion. These remarkable mechanisms might explain the high incidence of mucormycosis in COVID-19 patients with diabetes and, therefore, suggest regulation of GRP78 expression, management of glycemia and glucocorticoid treatment as potential therapeutic targets of this severe coinfection.The viral outbreak of severe acute respiratory syndrome coronavirus 2 emerged in China by the end of 2019 and was declared a global pandemic in early 2020. Along with the growing number of fatalities and lack of specific treatment at the time, the increasing incidence of mucormycosis worried World health agencies, as it ran the risk of more threatening outcomes for COVID-19 patients. In this context, this review aims to assemble case reports of COVID-19 associated mucormycosis and discuss virulence and host factors involved in the progress of these infections – key aspects that might unveil biological targets and pharmacological approaches to treat these infections. Recently, elevated serum iron levels during SARS-CoV-2 infection have been reported in the literature. Besides being a clinical characteristic of diabetic patients, iron overload is described as a risk factor for Rhizopus oryzae infection. Furthermore, the increased expression of human heat-shock protein GRP78 during iron overload and coronavirus infection displays a crucial role as a mediator in Mucorales invasion. These remarkable mechanisms might explain the high incidence of mucormycosis in COVID-19 patients with diabetes and, therefore, suggest regulation of GRP78 expression, management of glycemia and glucocorticoid treatment as potential therapeutic targets of this severe coinfection.HCPA/FAMED/UFRGS2023-09-05info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionPeer-reviewed ArticleAvaliados por Paresapplication/pdfhttps://seer.ufrgs.br/index.php/hcpa/article/view/122904Clinical & Biomedical Research; Vol. 43 No. 2 (2023): Clinical and Biomedical ResearchClinical and Biomedical Research; v. 43 n. 2 (2023): Clinical and Biomedical Research2357-9730reponame:Clinical and Biomedical Researchinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSporhttps://seer.ufrgs.br/index.php/hcpa/article/view/122904/89710Copyright (c) 2023 Manoela Mace, Bárbara Souza da Costa, Rubia do Nascimento Fuentefria, Alexandre Meneghello Fuentefriahttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessMace, ManoelaSouza da Costa, Bárbarado Nascimento Fuentefria, RubiaMeneghello Fuentefria, Alexandre2024-01-19T14:11:21Zoai:seer.ufrgs.br:article/122904Revistahttps://www.seer.ufrgs.br/index.php/hcpaPUBhttps://seer.ufrgs.br/index.php/hcpa/oai||cbr@hcpa.edu.br2357-97302357-9730opendoar:2024-01-19T14:11:21Clinical and Biomedical Research - Universidade Federal do Rio Grande do Sul (UFRGS)false |
dc.title.none.fl_str_mv |
Iron and glucose-regulated protein 78: fundamental components in the coinfection of Rhizopus oryzae and SARS-CoV-2 Iron and glucose-regulated protein 78: fundamental components in the coinfection of Rhizopus oryzae and SARS-CoV-2 |
title |
Iron and glucose-regulated protein 78: fundamental components in the coinfection of Rhizopus oryzae and SARS-CoV-2 |
spellingShingle |
Iron and glucose-regulated protein 78: fundamental components in the coinfection of Rhizopus oryzae and SARS-CoV-2 Mace, Manoela SARS-CoV-2 Infections COVID-19 Iron GRP78 Mucormycosis |
title_short |
Iron and glucose-regulated protein 78: fundamental components in the coinfection of Rhizopus oryzae and SARS-CoV-2 |
title_full |
Iron and glucose-regulated protein 78: fundamental components in the coinfection of Rhizopus oryzae and SARS-CoV-2 |
title_fullStr |
Iron and glucose-regulated protein 78: fundamental components in the coinfection of Rhizopus oryzae and SARS-CoV-2 |
title_full_unstemmed |
Iron and glucose-regulated protein 78: fundamental components in the coinfection of Rhizopus oryzae and SARS-CoV-2 |
title_sort |
Iron and glucose-regulated protein 78: fundamental components in the coinfection of Rhizopus oryzae and SARS-CoV-2 |
author |
Mace, Manoela |
author_facet |
Mace, Manoela Souza da Costa, Bárbara do Nascimento Fuentefria, Rubia Meneghello Fuentefria, Alexandre |
author_role |
author |
author2 |
Souza da Costa, Bárbara do Nascimento Fuentefria, Rubia Meneghello Fuentefria, Alexandre |
author2_role |
author author author |
dc.contributor.author.fl_str_mv |
Mace, Manoela Souza da Costa, Bárbara do Nascimento Fuentefria, Rubia Meneghello Fuentefria, Alexandre |
dc.subject.por.fl_str_mv |
SARS-CoV-2 Infections COVID-19 Iron GRP78 Mucormycosis |
topic |
SARS-CoV-2 Infections COVID-19 Iron GRP78 Mucormycosis |
description |
The viral outbreak of severe acute respiratory syndrome coronavirus 2 emerged in China by the end of 2019 and was declared a global pandemic in early 2020. Along with the growing number of fatalities and lack of specific treatment at the time, the increasing incidence of mucormycosis worried World health agencies, as it ran the risk of more threatening outcomes for COVID-19 patients. In this context, this review aims to assemble case reports of COVID-19 associated mucormycosis and discuss virulence and host factors involved in the progress of these infections – key aspects that might unveil biological targets and pharmacological approaches to treat these infections. Recently, elevated serum iron levels during SARS-CoV-2 infection have been reported in the literature. Besides being a clinical characteristic of diabetic patients, iron overload is described as a risk factor for Rhizopus oryzae infection. Furthermore, the increased expression of human heat-shock protein GRP78 during iron overload and coronavirus infection displays a crucial role as a mediator in Mucorales invasion. These remarkable mechanisms might explain the high incidence of mucormycosis in COVID-19 patients with diabetes and, therefore, suggest regulation of GRP78 expression, management of glycemia and glucocorticoid treatment as potential therapeutic targets of this severe coinfection. |
publishDate |
2023 |
dc.date.none.fl_str_mv |
2023-09-05 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion Peer-reviewed Article Avaliados por Pares |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://seer.ufrgs.br/index.php/hcpa/article/view/122904 |
url |
https://seer.ufrgs.br/index.php/hcpa/article/view/122904 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.none.fl_str_mv |
https://seer.ufrgs.br/index.php/hcpa/article/view/122904/89710 |
dc.rights.driver.fl_str_mv |
https://creativecommons.org/licenses/by/4.0 info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by/4.0 |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
HCPA/FAMED/UFRGS |
publisher.none.fl_str_mv |
HCPA/FAMED/UFRGS |
dc.source.none.fl_str_mv |
Clinical & Biomedical Research; Vol. 43 No. 2 (2023): Clinical and Biomedical Research Clinical and Biomedical Research; v. 43 n. 2 (2023): Clinical and Biomedical Research 2357-9730 reponame:Clinical and Biomedical Research instname:Universidade Federal do Rio Grande do Sul (UFRGS) instacron:UFRGS |
instname_str |
Universidade Federal do Rio Grande do Sul (UFRGS) |
instacron_str |
UFRGS |
institution |
UFRGS |
reponame_str |
Clinical and Biomedical Research |
collection |
Clinical and Biomedical Research |
repository.name.fl_str_mv |
Clinical and Biomedical Research - Universidade Federal do Rio Grande do Sul (UFRGS) |
repository.mail.fl_str_mv |
||cbr@hcpa.edu.br |
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1799767056362504192 |