Cargando…

Influenza infection rewires energy metabolism and induces browning features in adipose cells and tissues

Like all obligate intracellular pathogens, influenza A virus (IAV) reprograms host cell’s glucose and lipid metabolism to promote its own replication. However, the impact of influenza infection on white adipose tissue (WAT), a key tissue in the control of systemic energy homeostasis, has not been ye...

Descripción completa

Detalles Bibliográficos
Autores principales: Ayari, Asma, Rosa-Calatrava, Manuel, Lancel, Steve, Barthelemy, Johanna, Pizzorno, Andrés, Mayeuf-Louchart, Alicia, Baron, Morgane, Hot, David, Deruyter, Lucie, Soulard, Daphnée, Julien, Thomas, Faveeuw, Christelle, Molendi-Coste, Olivier, Dombrowicz, David, Sedano, Laura, Sencio, Valentin, Le Goffic, Ronan, Trottein, François, Wolowczuk, Isabelle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7224208/
https://www.ncbi.nlm.nih.gov/pubmed/32409640
http://dx.doi.org/10.1038/s42003-020-0965-6
_version_ 1783533858454503424
author Ayari, Asma
Rosa-Calatrava, Manuel
Lancel, Steve
Barthelemy, Johanna
Pizzorno, Andrés
Mayeuf-Louchart, Alicia
Baron, Morgane
Hot, David
Deruyter, Lucie
Soulard, Daphnée
Julien, Thomas
Faveeuw, Christelle
Molendi-Coste, Olivier
Dombrowicz, David
Sedano, Laura
Sencio, Valentin
Le Goffic, Ronan
Trottein, François
Wolowczuk, Isabelle
author_facet Ayari, Asma
Rosa-Calatrava, Manuel
Lancel, Steve
Barthelemy, Johanna
Pizzorno, Andrés
Mayeuf-Louchart, Alicia
Baron, Morgane
Hot, David
Deruyter, Lucie
Soulard, Daphnée
Julien, Thomas
Faveeuw, Christelle
Molendi-Coste, Olivier
Dombrowicz, David
Sedano, Laura
Sencio, Valentin
Le Goffic, Ronan
Trottein, François
Wolowczuk, Isabelle
author_sort Ayari, Asma
collection PubMed
description Like all obligate intracellular pathogens, influenza A virus (IAV) reprograms host cell’s glucose and lipid metabolism to promote its own replication. However, the impact of influenza infection on white adipose tissue (WAT), a key tissue in the control of systemic energy homeostasis, has not been yet characterized. Here, we show that influenza infection induces alterations in whole-body glucose metabolism that persist long after the virus has been cleared. We report depot-specific changes in the WAT of IAV-infected mice, notably characterized by the appearance of thermogenic brown-like adipocytes within the subcutaneous fat depot. Importantly, viral RNA- and viral antigen-harboring cells are detected in the WAT of infected mice. Using in vitro approaches, we find that IAV infection enhances the expression of brown-adipogenesis-related genes in preadipocytes. Overall, our findings shed light on the role that the white adipose tissue, which lies at the crossroads of nutrition, metabolism and immunity, may play in influenza infection.
format Online
Article
Text
id pubmed-7224208
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-72242082020-05-20 Influenza infection rewires energy metabolism and induces browning features in adipose cells and tissues Ayari, Asma Rosa-Calatrava, Manuel Lancel, Steve Barthelemy, Johanna Pizzorno, Andrés Mayeuf-Louchart, Alicia Baron, Morgane Hot, David Deruyter, Lucie Soulard, Daphnée Julien, Thomas Faveeuw, Christelle Molendi-Coste, Olivier Dombrowicz, David Sedano, Laura Sencio, Valentin Le Goffic, Ronan Trottein, François Wolowczuk, Isabelle Commun Biol Article Like all obligate intracellular pathogens, influenza A virus (IAV) reprograms host cell’s glucose and lipid metabolism to promote its own replication. However, the impact of influenza infection on white adipose tissue (WAT), a key tissue in the control of systemic energy homeostasis, has not been yet characterized. Here, we show that influenza infection induces alterations in whole-body glucose metabolism that persist long after the virus has been cleared. We report depot-specific changes in the WAT of IAV-infected mice, notably characterized by the appearance of thermogenic brown-like adipocytes within the subcutaneous fat depot. Importantly, viral RNA- and viral antigen-harboring cells are detected in the WAT of infected mice. Using in vitro approaches, we find that IAV infection enhances the expression of brown-adipogenesis-related genes in preadipocytes. Overall, our findings shed light on the role that the white adipose tissue, which lies at the crossroads of nutrition, metabolism and immunity, may play in influenza infection. Nature Publishing Group UK 2020-05-14 /pmc/articles/PMC7224208/ /pubmed/32409640 http://dx.doi.org/10.1038/s42003-020-0965-6 Text en © The Author(s) 2020 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Ayari, Asma
Rosa-Calatrava, Manuel
Lancel, Steve
Barthelemy, Johanna
Pizzorno, Andrés
Mayeuf-Louchart, Alicia
Baron, Morgane
Hot, David
Deruyter, Lucie
Soulard, Daphnée
Julien, Thomas
Faveeuw, Christelle
Molendi-Coste, Olivier
Dombrowicz, David
Sedano, Laura
Sencio, Valentin
Le Goffic, Ronan
Trottein, François
Wolowczuk, Isabelle
Influenza infection rewires energy metabolism and induces browning features in adipose cells and tissues
title Influenza infection rewires energy metabolism and induces browning features in adipose cells and tissues
title_full Influenza infection rewires energy metabolism and induces browning features in adipose cells and tissues
title_fullStr Influenza infection rewires energy metabolism and induces browning features in adipose cells and tissues
title_full_unstemmed Influenza infection rewires energy metabolism and induces browning features in adipose cells and tissues
title_short Influenza infection rewires energy metabolism and induces browning features in adipose cells and tissues
title_sort influenza infection rewires energy metabolism and induces browning features in adipose cells and tissues
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7224208/
https://www.ncbi.nlm.nih.gov/pubmed/32409640
http://dx.doi.org/10.1038/s42003-020-0965-6
work_keys_str_mv AT ayariasma influenzainfectionrewiresenergymetabolismandinducesbrowningfeaturesinadiposecellsandtissues
AT rosacalatravamanuel influenzainfectionrewiresenergymetabolismandinducesbrowningfeaturesinadiposecellsandtissues
AT lancelsteve influenzainfectionrewiresenergymetabolismandinducesbrowningfeaturesinadiposecellsandtissues
AT barthelemyjohanna influenzainfectionrewiresenergymetabolismandinducesbrowningfeaturesinadiposecellsandtissues
AT pizzornoandres influenzainfectionrewiresenergymetabolismandinducesbrowningfeaturesinadiposecellsandtissues
AT mayeuflouchartalicia influenzainfectionrewiresenergymetabolismandinducesbrowningfeaturesinadiposecellsandtissues
AT baronmorgane influenzainfectionrewiresenergymetabolismandinducesbrowningfeaturesinadiposecellsandtissues
AT hotdavid influenzainfectionrewiresenergymetabolismandinducesbrowningfeaturesinadiposecellsandtissues
AT deruyterlucie influenzainfectionrewiresenergymetabolismandinducesbrowningfeaturesinadiposecellsandtissues
AT soularddaphnee influenzainfectionrewiresenergymetabolismandinducesbrowningfeaturesinadiposecellsandtissues
AT julienthomas influenzainfectionrewiresenergymetabolismandinducesbrowningfeaturesinadiposecellsandtissues
AT faveeuwchristelle influenzainfectionrewiresenergymetabolismandinducesbrowningfeaturesinadiposecellsandtissues
AT molendicosteolivier influenzainfectionrewiresenergymetabolismandinducesbrowningfeaturesinadiposecellsandtissues
AT dombrowiczdavid influenzainfectionrewiresenergymetabolismandinducesbrowningfeaturesinadiposecellsandtissues
AT sedanolaura influenzainfectionrewiresenergymetabolismandinducesbrowningfeaturesinadiposecellsandtissues
AT senciovalentin influenzainfectionrewiresenergymetabolismandinducesbrowningfeaturesinadiposecellsandtissues
AT legofficronan influenzainfectionrewiresenergymetabolismandinducesbrowningfeaturesinadiposecellsandtissues
AT trotteinfrancois influenzainfectionrewiresenergymetabolismandinducesbrowningfeaturesinadiposecellsandtissues
AT wolowczukisabelle influenzainfectionrewiresenergymetabolismandinducesbrowningfeaturesinadiposecellsandtissues