tetano
Editor, Senior Moderator
Nat Commun
. 2023 Sep 26;14(1):5990.
doi: 10.1038/s41467-023-41761-1. Previous infection with seasonal coronaviruses does not protect male Syrian hamsters from challenge with SARS-CoV-2
Magen E Francis[SUP] 1 2 [/SUP], Ethan B Jansen[SUP] 1 2 [/SUP], Anthony Yourkowski[SUP] 1 2 [/SUP], Alaa Selim[SUP] 1 2 [/SUP], Cynthia L Swan[SUP] 1 [/SUP], Brian K MacPhee[SUP] 1 2 [/SUP], Brittany Thivierge[SUP] 1 [/SUP], Rachelle Buchanan[SUP] 1 [/SUP], Kerry J Lavender[SUP] 2 [/SUP], Joseph Darbellay[SUP] 1 [/SUP], Matthew B Rogers[SUP] 1 [/SUP], Jocelyne Lew[SUP] 1 [/SUP], Volker Gerdts[SUP] 1 [/SUP], Darryl Falzarano[SUP] 1 [/SUP], Danuta M Skowronski[SUP] 3 4 [/SUP], Calvin Sjaarda[SUP] 5 6 [/SUP], Alyson A Kelvin[SUP] 7 8 [/SUP]
Affiliations
SARS-CoV-2 variants and seasonal coronaviruses continue to cause disease and coronaviruses in the animal reservoir pose a constant spillover threat. Importantly, understanding of how previous infection may influence future exposures, especially in the context of seasonal coronaviruses and SARS-CoV-2 variants, is still limited. Here we adopted a step-wise experimental approach to examine the primary immune response and subsequent immune recall toward antigenically distinct coronaviruses using male Syrian hamsters. Hamsters were initially inoculated with seasonal coronaviruses (HCoV-NL63, HCoV-229E, or HCoV-OC43), or SARS-CoV-2 pango B lineage virus, then challenged with SARS-CoV-2 pango B lineage virus, or SARS-CoV-2 variants Beta or Omicron. Although infection with seasonal coronaviruses offered little protection against SARS-CoV-2 challenge, HCoV-NL63-infected animals had an increase of the previously elicited HCoV-NL63-specific neutralizing antibodies during challenge with SARS-CoV-2. On the other hand, primary infection with HCoV-OC43 induced distinct T cell gene signatures. Gene expression profiling indicated interferon responses and germinal center reactions to be induced during more similar primary infection-challenge combinations while signatures of increased inflammation as well as suppression of the antiviral response were observed following antigenically distant viral challenges. This work characterizes and analyzes seasonal coronaviruses effect on SARS-CoV-2 secondary infection and the findings are important for pan-coronavirus vaccine design.
. 2023 Sep 26;14(1):5990.
doi: 10.1038/s41467-023-41761-1. Previous infection with seasonal coronaviruses does not protect male Syrian hamsters from challenge with SARS-CoV-2
Magen E Francis[SUP] 1 2 [/SUP], Ethan B Jansen[SUP] 1 2 [/SUP], Anthony Yourkowski[SUP] 1 2 [/SUP], Alaa Selim[SUP] 1 2 [/SUP], Cynthia L Swan[SUP] 1 [/SUP], Brian K MacPhee[SUP] 1 2 [/SUP], Brittany Thivierge[SUP] 1 [/SUP], Rachelle Buchanan[SUP] 1 [/SUP], Kerry J Lavender[SUP] 2 [/SUP], Joseph Darbellay[SUP] 1 [/SUP], Matthew B Rogers[SUP] 1 [/SUP], Jocelyne Lew[SUP] 1 [/SUP], Volker Gerdts[SUP] 1 [/SUP], Darryl Falzarano[SUP] 1 [/SUP], Danuta M Skowronski[SUP] 3 4 [/SUP], Calvin Sjaarda[SUP] 5 6 [/SUP], Alyson A Kelvin[SUP] 7 8 [/SUP]
Affiliations
- PMID: 37752151
- DOI: 10.1038/s41467-023-41761-1
SARS-CoV-2 variants and seasonal coronaviruses continue to cause disease and coronaviruses in the animal reservoir pose a constant spillover threat. Importantly, understanding of how previous infection may influence future exposures, especially in the context of seasonal coronaviruses and SARS-CoV-2 variants, is still limited. Here we adopted a step-wise experimental approach to examine the primary immune response and subsequent immune recall toward antigenically distinct coronaviruses using male Syrian hamsters. Hamsters were initially inoculated with seasonal coronaviruses (HCoV-NL63, HCoV-229E, or HCoV-OC43), or SARS-CoV-2 pango B lineage virus, then challenged with SARS-CoV-2 pango B lineage virus, or SARS-CoV-2 variants Beta or Omicron. Although infection with seasonal coronaviruses offered little protection against SARS-CoV-2 challenge, HCoV-NL63-infected animals had an increase of the previously elicited HCoV-NL63-specific neutralizing antibodies during challenge with SARS-CoV-2. On the other hand, primary infection with HCoV-OC43 induced distinct T cell gene signatures. Gene expression profiling indicated interferon responses and germinal center reactions to be induced during more similar primary infection-challenge combinations while signatures of increased inflammation as well as suppression of the antiviral response were observed following antigenically distant viral challenges. This work characterizes and analyzes seasonal coronaviruses effect on SARS-CoV-2 secondary infection and the findings are important for pan-coronavirus vaccine design.