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Human Adenovirus and Influenza A Virus Exacerbate SARS-CoV-2 Infection in Animal Models

In this study, we investigated the features of the infectious process by simulating co-infection with SARS-CoV-2 and human adenovirus type 5 (HAdV-5) or influenza A virus (IAV) in vitro and in vivo. The determination of infectious activity of viruses and digital PCR demonstrated that during simultan...

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Autores principales: Svyatchenko, Victor A., Ternovoi, Vladimir A., Lutkovskiy, Roman Y., Protopopova, Elena V., Gudymo, Andrei S., Danilchenko, Nataliya V., Susloparov, Ivan M., Kolosova, Nataliya P., Ryzhikov, Alexander B., Taranov, Oleg S., Omigov, Vladimir V., Gavrilova, Elena V., Agafonov, Alexander P., Maksyutov, Rinat A., Loktev, Valery B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9860643/
https://www.ncbi.nlm.nih.gov/pubmed/36677472
http://dx.doi.org/10.3390/microorganisms11010180
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author Svyatchenko, Victor A.
Ternovoi, Vladimir A.
Lutkovskiy, Roman Y.
Protopopova, Elena V.
Gudymo, Andrei S.
Danilchenko, Nataliya V.
Susloparov, Ivan M.
Kolosova, Nataliya P.
Ryzhikov, Alexander B.
Taranov, Oleg S.
Omigov, Vladimir V.
Gavrilova, Elena V.
Agafonov, Alexander P.
Maksyutov, Rinat A.
Loktev, Valery B.
author_facet Svyatchenko, Victor A.
Ternovoi, Vladimir A.
Lutkovskiy, Roman Y.
Protopopova, Elena V.
Gudymo, Andrei S.
Danilchenko, Nataliya V.
Susloparov, Ivan M.
Kolosova, Nataliya P.
Ryzhikov, Alexander B.
Taranov, Oleg S.
Omigov, Vladimir V.
Gavrilova, Elena V.
Agafonov, Alexander P.
Maksyutov, Rinat A.
Loktev, Valery B.
author_sort Svyatchenko, Victor A.
collection PubMed
description In this study, we investigated the features of the infectious process by simulating co-infection with SARS-CoV-2 and human adenovirus type 5 (HAdV-5) or influenza A virus (IAV) in vitro and in vivo. The determination of infectious activity of viruses and digital PCR demonstrated that during simultaneous and sequential HAdV-5 followed by SARS-CoV-2 infection in vitro and in vivo, the HAdV-5 infection does not interfere with replication of SARS-CoV-2. The hamsters co-infected and mono-infected with SARS-CoV-2 exhibited nearly identical viral titers and viral loads of SARS-CoV-2 in the lungs. The hamsters and ferrets co-infected by SARS-CoV-2- and IAV demonstrated more pronounced clinical manifestations than mono-infected animals. Additionally, the lung histological data illustrate that HAdV-5 or IAV and SARS-CoV-2 co-infection induces more severe pathological changes in the lungs than mono-infection. The expression of several genes specific to interferon and cytokine signaling pathways in the lungs of co-infected hamsters was more upregulated compared to single infected with SARS-CoV-2 animals. Thus, co-infection with HAdV-5 or IAV and SARS-CoV-2 leads to more severe pulmonary disease in animals.
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spelling pubmed-98606432023-01-22 Human Adenovirus and Influenza A Virus Exacerbate SARS-CoV-2 Infection in Animal Models Svyatchenko, Victor A. Ternovoi, Vladimir A. Lutkovskiy, Roman Y. Protopopova, Elena V. Gudymo, Andrei S. Danilchenko, Nataliya V. Susloparov, Ivan M. Kolosova, Nataliya P. Ryzhikov, Alexander B. Taranov, Oleg S. Omigov, Vladimir V. Gavrilova, Elena V. Agafonov, Alexander P. Maksyutov, Rinat A. Loktev, Valery B. Microorganisms Article In this study, we investigated the features of the infectious process by simulating co-infection with SARS-CoV-2 and human adenovirus type 5 (HAdV-5) or influenza A virus (IAV) in vitro and in vivo. The determination of infectious activity of viruses and digital PCR demonstrated that during simultaneous and sequential HAdV-5 followed by SARS-CoV-2 infection in vitro and in vivo, the HAdV-5 infection does not interfere with replication of SARS-CoV-2. The hamsters co-infected and mono-infected with SARS-CoV-2 exhibited nearly identical viral titers and viral loads of SARS-CoV-2 in the lungs. The hamsters and ferrets co-infected by SARS-CoV-2- and IAV demonstrated more pronounced clinical manifestations than mono-infected animals. Additionally, the lung histological data illustrate that HAdV-5 or IAV and SARS-CoV-2 co-infection induces more severe pathological changes in the lungs than mono-infection. The expression of several genes specific to interferon and cytokine signaling pathways in the lungs of co-infected hamsters was more upregulated compared to single infected with SARS-CoV-2 animals. Thus, co-infection with HAdV-5 or IAV and SARS-CoV-2 leads to more severe pulmonary disease in animals. MDPI 2023-01-11 /pmc/articles/PMC9860643/ /pubmed/36677472 http://dx.doi.org/10.3390/microorganisms11010180 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Svyatchenko, Victor A.
Ternovoi, Vladimir A.
Lutkovskiy, Roman Y.
Protopopova, Elena V.
Gudymo, Andrei S.
Danilchenko, Nataliya V.
Susloparov, Ivan M.
Kolosova, Nataliya P.
Ryzhikov, Alexander B.
Taranov, Oleg S.
Omigov, Vladimir V.
Gavrilova, Elena V.
Agafonov, Alexander P.
Maksyutov, Rinat A.
Loktev, Valery B.
Human Adenovirus and Influenza A Virus Exacerbate SARS-CoV-2 Infection in Animal Models
title Human Adenovirus and Influenza A Virus Exacerbate SARS-CoV-2 Infection in Animal Models
title_full Human Adenovirus and Influenza A Virus Exacerbate SARS-CoV-2 Infection in Animal Models
title_fullStr Human Adenovirus and Influenza A Virus Exacerbate SARS-CoV-2 Infection in Animal Models
title_full_unstemmed Human Adenovirus and Influenza A Virus Exacerbate SARS-CoV-2 Infection in Animal Models
title_short Human Adenovirus and Influenza A Virus Exacerbate SARS-CoV-2 Infection in Animal Models
title_sort human adenovirus and influenza a virus exacerbate sars-cov-2 infection in animal models
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9860643/
https://www.ncbi.nlm.nih.gov/pubmed/36677472
http://dx.doi.org/10.3390/microorganisms11010180
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