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Candidate genes of SARS-CoV-2 gender susceptibility

The severe acute respiratory syndrome coronavirus (SARS-CoV-2) initiated a global viral pandemic since late 2019. Understanding that Coronavirus disease (COVID-19) disproportionately affects men than women results in great challenges. Although there is a growing body of published study on this topic...

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Autores principales: Russo, Cristina, Morello, Giovanna, Malaguarnera, Roberta, Piro, Salvatore, Furno, Debora Lo, Malaguarnera, Lucia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8578384/
https://www.ncbi.nlm.nih.gov/pubmed/34753980
http://dx.doi.org/10.1038/s41598-021-01131-7
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author Russo, Cristina
Morello, Giovanna
Malaguarnera, Roberta
Piro, Salvatore
Furno, Debora Lo
Malaguarnera, Lucia
author_facet Russo, Cristina
Morello, Giovanna
Malaguarnera, Roberta
Piro, Salvatore
Furno, Debora Lo
Malaguarnera, Lucia
author_sort Russo, Cristina
collection PubMed
description The severe acute respiratory syndrome coronavirus (SARS-CoV-2) initiated a global viral pandemic since late 2019. Understanding that Coronavirus disease (COVID-19) disproportionately affects men than women results in great challenges. Although there is a growing body of published study on this topic, effective explanations underlying these sex differences and their effects on the infection outcome still remain uncertain. We applied a holistic bioinformatics method to investigate molecular variations of known SARS-CoV-2 interacting human proteins mainly expressed in gonadal tissues (testis and ovary), allowing for the identification of potential genetic targets for this infection. Functional enrichment and interaction network analyses were also performed to better investigate the biological differences between testicular and ovarian responses in the SARS-CoV-2 infection, paying particular attention to genes linked to immune-related pathways, reactions of host cells after intracellular infection, steroid hormone biosynthesis, receptor signaling, and the complement cascade, in order to evaluate their potential association with sexual difference in the likelihood of infection and severity of symptoms. The analysis revealed that within the testis network TMPRSS2, ADAM10, SERPING1, and CCR5 were present, while within the ovary network we found BST2, GATA1, ENPEP, TLR4, TLR7, IRF1, and IRF2. Our findings could provide potential targets for forthcoming experimental investigation related to SARS-CoV-2 treatment.
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spelling pubmed-85783842021-11-10 Candidate genes of SARS-CoV-2 gender susceptibility Russo, Cristina Morello, Giovanna Malaguarnera, Roberta Piro, Salvatore Furno, Debora Lo Malaguarnera, Lucia Sci Rep Article The severe acute respiratory syndrome coronavirus (SARS-CoV-2) initiated a global viral pandemic since late 2019. Understanding that Coronavirus disease (COVID-19) disproportionately affects men than women results in great challenges. Although there is a growing body of published study on this topic, effective explanations underlying these sex differences and their effects on the infection outcome still remain uncertain. We applied a holistic bioinformatics method to investigate molecular variations of known SARS-CoV-2 interacting human proteins mainly expressed in gonadal tissues (testis and ovary), allowing for the identification of potential genetic targets for this infection. Functional enrichment and interaction network analyses were also performed to better investigate the biological differences between testicular and ovarian responses in the SARS-CoV-2 infection, paying particular attention to genes linked to immune-related pathways, reactions of host cells after intracellular infection, steroid hormone biosynthesis, receptor signaling, and the complement cascade, in order to evaluate their potential association with sexual difference in the likelihood of infection and severity of symptoms. The analysis revealed that within the testis network TMPRSS2, ADAM10, SERPING1, and CCR5 were present, while within the ovary network we found BST2, GATA1, ENPEP, TLR4, TLR7, IRF1, and IRF2. Our findings could provide potential targets for forthcoming experimental investigation related to SARS-CoV-2 treatment. Nature Publishing Group UK 2021-11-09 /pmc/articles/PMC8578384/ /pubmed/34753980 http://dx.doi.org/10.1038/s41598-021-01131-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Russo, Cristina
Morello, Giovanna
Malaguarnera, Roberta
Piro, Salvatore
Furno, Debora Lo
Malaguarnera, Lucia
Candidate genes of SARS-CoV-2 gender susceptibility
title Candidate genes of SARS-CoV-2 gender susceptibility
title_full Candidate genes of SARS-CoV-2 gender susceptibility
title_fullStr Candidate genes of SARS-CoV-2 gender susceptibility
title_full_unstemmed Candidate genes of SARS-CoV-2 gender susceptibility
title_short Candidate genes of SARS-CoV-2 gender susceptibility
title_sort candidate genes of sars-cov-2 gender susceptibility
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8578384/
https://www.ncbi.nlm.nih.gov/pubmed/34753980
http://dx.doi.org/10.1038/s41598-021-01131-7
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