Increased lethality in influenza and SARS-CoV-2 coinfection is prevented by influenza immunity but not SARS-CoV-2 immunity

Nat Commun. 2021 Oct 5;12(1):5819. doi: 10.1038/s41467-021-26113-1.

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.

MeSH terms

  • Angiotensin-Converting Enzyme 2 / metabolism
  • Animals
  • Antibodies, Viral / immunology
  • COVID-19 / immunology*
  • COVID-19 / pathology
  • COVID-19 / virology*
  • Cell Line
  • Coinfection / immunology*
  • Coinfection / virology*
  • Disease Models, Animal
  • Female
  • Humans
  • Immunity*
  • Inflammation / genetics
  • Lung / pathology
  • Lung / virology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Orthomyxoviridae Infections / immunology*
  • Orthomyxoviridae Infections / virology*
  • SARS-CoV-2 / immunology*
  • Up-Regulation / genetics
  • Viral Load / immunology

Substances

  • Antibodies, Viral
  • Angiotensin-Converting Enzyme 2