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The elucidation of plasma lipidome profiles during severe influenza in a mouse model

Although influenza virus infection has been shown to affect lipid metabolism, details remain unknown. Therefore, we elucidated the kinetic lipid profiles of mice infected with different doses of influenza virus A/Puerto Rico/8/34 (H1N1) (PR8) by measuring multiple lipid molecular species using untar...

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Autores principales: Ohno, Marumi, Gowda, Siddabasave Gowda B., Sekiya, Toshiki, Nomura, Naoki, Shingai, Masashi, Hui, Shu-Ping, Kida, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10469212/
https://www.ncbi.nlm.nih.gov/pubmed/37648726
http://dx.doi.org/10.1038/s41598-023-41055-y
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author Ohno, Marumi
Gowda, Siddabasave Gowda B.
Sekiya, Toshiki
Nomura, Naoki
Shingai, Masashi
Hui, Shu-Ping
Kida, Hiroshi
author_facet Ohno, Marumi
Gowda, Siddabasave Gowda B.
Sekiya, Toshiki
Nomura, Naoki
Shingai, Masashi
Hui, Shu-Ping
Kida, Hiroshi
author_sort Ohno, Marumi
collection PubMed
description Although influenza virus infection has been shown to affect lipid metabolism, details remain unknown. Therefore, we elucidated the kinetic lipid profiles of mice infected with different doses of influenza virus A/Puerto Rico/8/34 (H1N1) (PR8) by measuring multiple lipid molecular species using untargeted lipidomic analysis. C57BL/6 male mice were intranasally infected with PR8 virus at 50 or 500 plaque-forming units to cause sublethal or lethal influenza, respectively. Plasma and tissue samples were collected at 1, 3, and 6 days post-infection (dpi), and comprehensive lipidomic analysis was performed using high-performance liquid chromatography–linear trap quadrupole–Orbitrap mass spectrometry, as well as gene expression analyses. The most prominent feature of the lipid profile in lethally infected mice was the elevated plasma concentrations of phosphatidylethanolamines (PEs) containing polyunsaturated fatty acid (PUFA) at 3 dpi. Furthermore, the facilitation of PUFA-containing phospholipid production in the lungs, but not in the liver, was suggested by gene expression and lipidomic analysis of tissue samples. Given the increased plasma or serum levels of PUFA-containing PEs in patients with other viral infections, especially in severe cases, the elevation of these phospholipids in circulation could be a biomarker of infection and the severity of infectious diseases.
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spelling pubmed-104692122023-09-01 The elucidation of plasma lipidome profiles during severe influenza in a mouse model Ohno, Marumi Gowda, Siddabasave Gowda B. Sekiya, Toshiki Nomura, Naoki Shingai, Masashi Hui, Shu-Ping Kida, Hiroshi Sci Rep Article Although influenza virus infection has been shown to affect lipid metabolism, details remain unknown. Therefore, we elucidated the kinetic lipid profiles of mice infected with different doses of influenza virus A/Puerto Rico/8/34 (H1N1) (PR8) by measuring multiple lipid molecular species using untargeted lipidomic analysis. C57BL/6 male mice were intranasally infected with PR8 virus at 50 or 500 plaque-forming units to cause sublethal or lethal influenza, respectively. Plasma and tissue samples were collected at 1, 3, and 6 days post-infection (dpi), and comprehensive lipidomic analysis was performed using high-performance liquid chromatography–linear trap quadrupole–Orbitrap mass spectrometry, as well as gene expression analyses. The most prominent feature of the lipid profile in lethally infected mice was the elevated plasma concentrations of phosphatidylethanolamines (PEs) containing polyunsaturated fatty acid (PUFA) at 3 dpi. Furthermore, the facilitation of PUFA-containing phospholipid production in the lungs, but not in the liver, was suggested by gene expression and lipidomic analysis of tissue samples. Given the increased plasma or serum levels of PUFA-containing PEs in patients with other viral infections, especially in severe cases, the elevation of these phospholipids in circulation could be a biomarker of infection and the severity of infectious diseases. Nature Publishing Group UK 2023-08-30 /pmc/articles/PMC10469212/ /pubmed/37648726 http://dx.doi.org/10.1038/s41598-023-41055-y Text en © The Author(s) 2023 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
Ohno, Marumi
Gowda, Siddabasave Gowda B.
Sekiya, Toshiki
Nomura, Naoki
Shingai, Masashi
Hui, Shu-Ping
Kida, Hiroshi
The elucidation of plasma lipidome profiles during severe influenza in a mouse model
title The elucidation of plasma lipidome profiles during severe influenza in a mouse model
title_full The elucidation of plasma lipidome profiles during severe influenza in a mouse model
title_fullStr The elucidation of plasma lipidome profiles during severe influenza in a mouse model
title_full_unstemmed The elucidation of plasma lipidome profiles during severe influenza in a mouse model
title_short The elucidation of plasma lipidome profiles during severe influenza in a mouse model
title_sort elucidation of plasma lipidome profiles during severe influenza in a mouse model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10469212/
https://www.ncbi.nlm.nih.gov/pubmed/37648726
http://dx.doi.org/10.1038/s41598-023-41055-y
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