Virulence Profiles of Wild-Type, P.1 and Delta SARS-CoV-2 Variants in K18-hACE2 Transgenic Mice

Author:

da Silva Santos Yasmin12,Gamon Thais Helena Martins3,de Azevedo Marcela Santiago Pacheco34ORCID,Telezynski Bruna Larotonda3,de Souza Edmarcia Elisa5,de Oliveira Danielle Bruna Leal36,Dombrowski Jamille Gregório4ORCID,Rosa-Fernandes Livia37,Palmisano Giuseppe78,de Moura Carvalho Leonardo José2,Luvizotto Maria Cecília Rui9,Wrenger Carsten5ORCID,Covas Dimas Tadeu1011,Curi Rui1213,Marinho Claudio Romero Farias4ORCID,Durigon Edison Luiz314ORCID,Epiphanio Sabrina1ORCID

Affiliation:

1. Laboratory of Cellular and Molecular Immunopathology of Malaria, Department of Clinical and Toxicological Analysis, Faculty of Pharmaceutical Sciences, University of São Paulo, São Paulo 05508-000, Brazil

2. Laboratory of Malaria Research, Oswaldo Cruz Institute, Oswaldo Cruz Foundation, Rio de Janeiro 21040-900, Brazil

3. Laboratory of Clinical and Molecular Virology, Department of Microbiology, Institute of Biomedical Sciences, University of São Paulo, São Paulo 05508-000, Brazil

4. Laboratory of Experimental Immunoparasitology, Department of Parasitology, Institute of Biomedical Sciences, University of São Paulo, São Paulo 05508-000, Brazil

5. Unit for Drug Discovery, Department of Parasitology, Institute of Biomedical Sciences, University of São Paulo, São Paulo 05508-000, Brazil

6. Hospital Israelita Albert Einstein, São Paulo 05652-900, Brazil

7. GlycoProteomics Laboratory, Department of Parasitology, ICB, University of São Paulo, São Paulo 05508-000, Brazil

8. School of Natural Sciences, Macquarie University, Sydney 2109, Australia

9. School of Veterinary Medicine of Araçatuba, São Paulo State University, São Paulo 16050-680, Brazil

10. Butantan Institute, São Paulo 05508-040, Brazil

11. Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto 14049-900, Brazil

12. Interdisciplinary Program of Health Sciences, Cruzeiro do Sul University, São Paulo 08060-070, Brazil

13. Immunobiological Production Section, Bioindustrial Center, Butantan Institute, São Paulo 05503-900, Brazil

14. Scientific Plataform Pasteur/USP, University of São Paulo, São Paulo 05508-020, Brazil

Abstract

Since December 2019, the world has been experiencing the COVID-19 pandemic caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), and we now face the emergence of several variants. We aimed to assess the differences between the wild-type (Wt) (Wuhan) strain and the P.1 (Gamma) and Delta variants using infected K18-hACE2 mice. The clinical manifestations, behavior, virus load, pulmonary capacity, and histopathological alterations were analyzed. The P.1-infected mice showed weight loss and more severe clinical manifestations of COVID-19 than the Wt and Delta-infected mice. The respiratory capacity was reduced in the P.1-infected mice compared to the other groups. Pulmonary histological findings demonstrated that a more aggressive disease was generated by the P.1 and Delta variants compared to the Wt strain of the virus. The quantification of the SARS-CoV-2 viral copies varied greatly among the infected mice although it was higher in P.1-infected mice on the day of death. Our data revealed that K18-hACE2 mice infected with the P.1 variant develop a more severe infectious disease than those infected with the other variants, despite the significant heterogeneity among the mice.

Funder

São Paulo Research Foundation-FAPESP

The National Council for Scientific and Technological Development-CNPq

Coordination for the Improvement of Higher Education Personnel-CAPES

Carlos Chagas Filho Foundation for Research Support of the State of Rio de Janeiro-FAPERJ

Oswaldo Cruz Foundation Rio de Janeiro-FIOCRUZ

Publisher

MDPI AG

Subject

Virology,Infectious Diseases

Reference70 articles.

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