Protection against reinfection with D614- or G614-SARS-CoV-2 isolates in hamsters
Brustolin, M.; Rodon, J.; Rodriguez de la Concepcion, M. L.; Avila-Nieto, C.; Cantero, G.; Perez, M.; Nigeer, T.; Noguera-Julian, M.; Guallar, V.; Valencia, A.; Roca, N.; Izquierdo-Useros, N.; Blanco, J.; Clotet, B.; Bensaid, A.; Carrillo, J.; Vergara-Alert, J.; Segales, J.
Show 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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