Author
Listed:
- Hagit Achdout
(Israel Institute for Biological Research)
- Einat. B. Vitner
(Israel Institute for Biological Research)
- Boaz Politi
(Israel Institute for Biological Research)
- Sharon Melamed
(Israel Institute for Biological Research)
- Yfat Yahalom-Ronen
(Israel Institute for Biological Research)
- Hadas Tamir
(Israel Institute for Biological Research)
- Noam Erez
(Israel Institute for Biological Research)
- Roy Avraham
(Israel Institute for Biological Research)
- Shay Weiss
(Israel Institute for Biological Research)
- Lilach Cherry
(Israel Institute for Biological Research)
- Erez Bar-Haim
(Israel Institute for Biological Research)
- Efi Makdasi
(Israel Institute for Biological Research)
- David Gur
(Israel Institute for Biological Research)
- Moshe Aftalion
(Israel Institute for Biological Research)
- Theodor Chitlaru
(Israel Institute for Biological Research)
- Yaron Vagima
(Israel Institute for Biological Research)
- Nir Paran
(Israel Institute for Biological Research)
- Tomer Israely
(Israel Institute for Biological Research)
Abstract
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the cause of the ongoing coronavirus disease 2019 (COVID-19) pandemic. The continued spread of SARS-CoV-2 increases the probability of influenza/SARS-CoV-2 coinfection, which may result in severe disease. In this study, we examine the disease outcome of influenza A virus (IAV) and SARS-CoV-2 coinfection in K18-hACE2 mice. Our data indicate enhance susceptibility of IAV-infected mice to developing severe disease upon coinfection with SARS-CoV-2 two days later. In contrast to nonfatal influenza and lower mortality rates due to SARS-CoV-2 alone, this coinfection results in severe morbidity and nearly complete mortality. Coinfection is associated with elevated influenza viral loads in respiratory organs. Remarkably, prior immunity to influenza, but not to SARS-CoV-2, prevents severe disease and mortality. This protection is antibody-dependent. These data experimentally support the necessity of seasonal influenza vaccination for reducing the risk of severe influenza/COVID-19 comorbidity during the COVID-19 pandemic.
Suggested Citation
Hagit Achdout & Einat. B. Vitner & Boaz Politi & Sharon Melamed & Yfat Yahalom-Ronen & Hadas Tamir & Noam Erez & Roy Avraham & Shay Weiss & Lilach Cherry & Erez Bar-Haim & Efi Makdasi & David Gur & Mo, 2021.
"Increased lethality in influenza and SARS-CoV-2 coinfection is prevented by influenza immunity but not SARS-CoV-2 immunity,"
Nature Communications, Nature, vol. 12(1), pages 1-10, December.
Handle:
RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-26113-1
DOI: 10.1038/s41467-021-26113-1
Download full text from publisher
Corrections
All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-26113-1. See general information about how to correct material in RePEc.
If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.
We have no bibliographic references for this item. You can help adding them by using this form .
If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.
For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .
Please note that corrections may take a couple of weeks to filter through
the various RePEc services.