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Protection against reinfection with D614- or G614-SARS-CoV-2 isolates in hamsters
Marco Brustolin; Jordi Rodon; Maria Luisa Rodriguez de la Concepcion; Carlos Avila-Nieto; Guillermo Cantero; Monica Perez; Te Nigeer; Marc Noguera-Julian; Victor Guallar; Alfonso Valencia; Nuria Roca; Nuria Izquierdo-Useros; Julia Blanco; Bonaventura Clotet; Albert Bensaid; Jorge Carrillo; Julia Vergara-Alert; Joaquim Segales.
Affiliation
  • Marco Brustolin; IRTA-CReSA
  • Jordi Rodon; IRTA-CRESA
  • Maria Luisa Rodriguez de la Concepcion; irsiCaixa Institute for AIDS research
  • Carlos Avila-Nieto; irsiCaixa Institute for AIDS research
  • Guillermo Cantero; IRTA-CReSA
  • Monica Perez; IRTA-CReSA
  • Te Nigeer; IRTA-CRESA
  • Marc Noguera-Julian; irsiCaixa Institute for AIDS research
  • Victor Guallar; Barcelona Supercomputing Center (BSC)
  • Alfonso Valencia; Barcelona Supercomputing Center (BSC)
  • Nuria Roca; IRTA-CReSA
  • Nuria Izquierdo-Useros; irsiCaixa Institute for AIDS research
  • Julia Blanco; irsiCaixa Institute for AIDS research
  • Bonaventura Clotet; irsiCaixa Institute for AIDS research
  • Albert Bensaid; IRTA-CReSA
  • Jorge Carrillo; irsiCaixa Institute for AIDS research
  • Julia Vergara-Alert; IRTA-CRESA
  • Joaquim Segales; IRTA-CReSA
Preprint in English | bioRxiv | ID: ppbiorxiv-425729
Journal article
A scientific journal published article is available and is probably based on this preprint. It has been identified through a machine matching algorithm, human confirmation is still pending.
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ABSTRACT
Reinfections with SARS-CoV-2 have already been documented in humans, although its real incidence is currently unknown. Besides having great impact on public health, this phenomenon raises the question if immunity generated by a single infection is sufficient to provide sterilizing/protective immunity to a subsequent SARS-CoV-2 re-exposure. The Golden Syrian hamster is a manageable animal model to explore immunological mechanisms able to counteract COVID-19, as it recapitulates pathological aspects of mild to moderately affected patients. Here, we report that SARS-CoV-2-inoculated hamsters resolve infection in the upper and lower respiratory tracts within seven days upon inoculation with the Cat01 (G614) SARS-CoV-2 isolate. Three weeks after primary challenge, and despite high titers of neutralizing antibodies, half of the animals were susceptible to reinfection by both identical (Cat01, G614) and variant (WA/1, D614) SARS-CoV-2 isolates. However, upon re-inoculation, only nasal tissues were transiently infected with much lower viral replication than those observed after the first inoculation. These data indicate that a primary SARS-CoV-2 infection is not sufficient to elicit a sterilizing immunity in hamster models but protects against lung disease.
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Full text: Available Collection: Preprints Database: bioRxiv Type of study: Observational study Language: English Year: 2021 Document type: Preprint
Full text: Available Collection: Preprints Database: bioRxiv Type of study: Observational study Language: English Year: 2021 Document type: Preprint
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