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Phospholipid analysis of two influenza A virus-infected cell lines differing in their viral replication kinetics
Fluctuations in phospholipid composition in infected cells during influenza A virus replication were analyzed using two different susceptible host cell lines: H292 cells, exhibiting a rapid cytopathic effect, and A549 cells, exhibiting a retarded cytopathic effect. Microarray analysis demonstrated t...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Vienna
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10080527/ https://www.ncbi.nlm.nih.gov/pubmed/37027089 http://dx.doi.org/10.1007/s00705-023-05766-x |
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author | Kawabata, Kohei Sato, Yuichiro Kubo, Takanori Tokumura, Akira Nishi, Hiroyuki Morimoto, Kinjiro |
author_facet | Kawabata, Kohei Sato, Yuichiro Kubo, Takanori Tokumura, Akira Nishi, Hiroyuki Morimoto, Kinjiro |
author_sort | Kawabata, Kohei |
collection | PubMed |
description | Fluctuations in phospholipid composition in infected cells during influenza A virus replication were analyzed using two different susceptible host cell lines: H292 cells, exhibiting a rapid cytopathic effect, and A549 cells, exhibiting a retarded cytopathic effect. Microarray analysis demonstrated that A549 cells recognized influenza A virus invasion, expression of pathogen recognition genes was affected, and antiviral genes were activated. On the other hand, H292 cells did not display such an antiviral state, and in these cells, rapid virus amplification and a rapid cytopathic effect were observed. Levels of ceramide, diacylglycerol, and lysolipids were higher in virus-infected cells than in the corresponding mock-infected cells at the later stages of infection. The accumulation of these lipids in IAV-infected cells occurred together with viral replication. The relationship between the characteristic features of ceramide, diacylglycerol, and lysolipid in the plasma membrane, where enveloped viruses are released, and their role in viral envelope formation are discussed. Our results indicate that viral replication disturbs cellular lipid metabolism, with consequences for viral replication kinetics. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00705-023-05766-x. |
format | Online Article Text |
id | pubmed-10080527 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Vienna |
record_format | MEDLINE/PubMed |
spelling | pubmed-100805272023-04-07 Phospholipid analysis of two influenza A virus-infected cell lines differing in their viral replication kinetics Kawabata, Kohei Sato, Yuichiro Kubo, Takanori Tokumura, Akira Nishi, Hiroyuki Morimoto, Kinjiro Arch Virol Original Article Fluctuations in phospholipid composition in infected cells during influenza A virus replication were analyzed using two different susceptible host cell lines: H292 cells, exhibiting a rapid cytopathic effect, and A549 cells, exhibiting a retarded cytopathic effect. Microarray analysis demonstrated that A549 cells recognized influenza A virus invasion, expression of pathogen recognition genes was affected, and antiviral genes were activated. On the other hand, H292 cells did not display such an antiviral state, and in these cells, rapid virus amplification and a rapid cytopathic effect were observed. Levels of ceramide, diacylglycerol, and lysolipids were higher in virus-infected cells than in the corresponding mock-infected cells at the later stages of infection. The accumulation of these lipids in IAV-infected cells occurred together with viral replication. The relationship between the characteristic features of ceramide, diacylglycerol, and lysolipid in the plasma membrane, where enveloped viruses are released, and their role in viral envelope formation are discussed. Our results indicate that viral replication disturbs cellular lipid metabolism, with consequences for viral replication kinetics. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00705-023-05766-x. Springer Vienna 2023-04-07 2023 /pmc/articles/PMC10080527/ /pubmed/37027089 http://dx.doi.org/10.1007/s00705-023-05766-x Text en © The Author(s), under exclusive licence to Springer-Verlag GmbH Austria, part of Springer Nature 2023, Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Original Article Kawabata, Kohei Sato, Yuichiro Kubo, Takanori Tokumura, Akira Nishi, Hiroyuki Morimoto, Kinjiro Phospholipid analysis of two influenza A virus-infected cell lines differing in their viral replication kinetics |
title | Phospholipid analysis of two influenza A virus-infected cell lines differing in their viral replication kinetics |
title_full | Phospholipid analysis of two influenza A virus-infected cell lines differing in their viral replication kinetics |
title_fullStr | Phospholipid analysis of two influenza A virus-infected cell lines differing in their viral replication kinetics |
title_full_unstemmed | Phospholipid analysis of two influenza A virus-infected cell lines differing in their viral replication kinetics |
title_short | Phospholipid analysis of two influenza A virus-infected cell lines differing in their viral replication kinetics |
title_sort | phospholipid analysis of two influenza a virus-infected cell lines differing in their viral replication kinetics |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10080527/ https://www.ncbi.nlm.nih.gov/pubmed/37027089 http://dx.doi.org/10.1007/s00705-023-05766-x |
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