Cells
(Aug 2022)
Impact of Microbiota Depletion by Antibiotics on SARS-CoV-2 Infection of K18-hACE2 Mice
Patrícia Brito Rodrigues,
Giovanni Freitas Gomes,
Monara K. S. C. Angelim,
Gabriela F. Souza,
Stefanie Primon Muraro,
Daniel A. Toledo-Teixeira,
Bruna Amanda Cruz Rattis,
Amanda Stephane Passos,
Laís Passarielo Pral,
Vinícius de Rezende Rodovalho,
Arilson Bernardo dos Santos P. Gomes,
Valquíria Aparecida Matheus,
André Saraiva Leão Marcelo Antunes,
Fernanda Crunfli,
Krist Helen Antunes,
Ana Paula Duarte de Souza,
Sílvio Roberto Consonni,
Luiz Osório Leiria,
José Carlos Alves-Filho,
Thiago M. Cunha,
Pedro M. M. Moraes-Vieira,
José Luiz Proença-Módena,
Marco Aurélio R. Vinolo
Affiliations
Patrícia Brito Rodrigues
Laboratory of Immunoinflammation, Institute of Biology, University of Campinas (UNICAMP), Campinas 13000-000, Brazil
Giovanni Freitas Gomes
Center of Research in Inflammatory Diseases, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto 14000-000, Brazil
Monara K. S. C. Angelim
Laboratory of Immunometabolism, Institute of Biology, University of Campinas (UNICAMP), Campinas 13000-000, Brazil
Gabriela F. Souza
Laboratory of Emerging Viruses, Institute of Biology, University of Campinas (UNICAMP), Campinas 13000-000, Brazil
Stefanie Primon Muraro
Laboratory of Emerging Viruses, Institute of Biology, University of Campinas (UNICAMP), Campinas 13000-000, Brazil
Daniel A. Toledo-Teixeira
Laboratory of Emerging Viruses, Institute of Biology, University of Campinas (UNICAMP), Campinas 13000-000, Brazil
Bruna Amanda Cruz Rattis
Department of Pathology, Faculty of Medicine of Ribeirão Preto, University of São Paulo, Ribeirão Preto 14000-000, Brazil
Amanda Stephane Passos
Center of Research in Inflammatory Diseases, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto 14000-000, Brazil
Laís Passarielo Pral
Laboratory of Immunoinflammation, Institute of Biology, University of Campinas (UNICAMP), Campinas 13000-000, Brazil
Vinícius de Rezende Rodovalho
Laboratory of Immunoinflammation, Institute of Biology, University of Campinas (UNICAMP), Campinas 13000-000, Brazil
Arilson Bernardo dos Santos P. Gomes
Laboratory of Immunoinflammation, Institute of Biology, University of Campinas (UNICAMP), Campinas 13000-000, Brazil
Valquíria Aparecida Matheus
Laboratory of Immunoinflammation, Institute of Biology, University of Campinas (UNICAMP), Campinas 13000-000, Brazil
André Saraiva Leão Marcelo Antunes
Laboratory of Neuroproteomics, Institute of Biology, University of Campinas (UNICAMP), Campinas 13000-000, Brazil
Fernanda Crunfli
Laboratory of Neuroproteomics, Institute of Biology, University of Campinas (UNICAMP), Campinas 13000-000, Brazil
Krist Helen Antunes
Laboratory of Clinical and Experimental Immunology, Pontifical Catholic University of Rio Grande do Sul, Porto Alegre 90000-000, Brazil
Ana Paula Duarte de Souza
Laboratory of Clinical and Experimental Immunology, Pontifical Catholic University of Rio Grande do Sul, Porto Alegre 90000-000, Brazil
Sílvio Roberto Consonni
Laboratory of Citochemistry and Immunocitochemistry, Institute of Biology, University of Campinas (UNICAMP), Campinas 13000-000, Brazil
Luiz Osório Leiria
Center of Research in Inflammatory Diseases, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto 14000-000, Brazil
José Carlos Alves-Filho
Center of Research in Inflammatory Diseases, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto 14000-000, Brazil
Thiago M. Cunha
Center of Research in Inflammatory Diseases, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto 14000-000, Brazil
Pedro M. M. Moraes-Vieira
Laboratory of Immunometabolism, Institute of Biology, University of Campinas (UNICAMP), Campinas 13000-000, Brazil
José Luiz Proença-Módena
Laboratory of Emerging Viruses, Institute of Biology, University of Campinas (UNICAMP), Campinas 13000-000, Brazil
Marco Aurélio R. Vinolo
Laboratory of Immunoinflammation, Institute of Biology, University of Campinas (UNICAMP), Campinas 13000-000, Brazil
DOI
https://doi.org/10.3390/cells11162572
Journal volume & issue
Vol. 11,
no. 16
p.
2572
Abstract
Read online
Clinical and experimental data indicate that severe acute respiratory syndrome coronavirus (SARS-CoV)-2 infection is associated with significant changes in the composition and function of intestinal microbiota. However, the relevance of these effects for SARS-CoV-2 pathophysiology is unknown. In this study, we analyzed the impact of microbiota depletion after antibiotic treatment on the clinical and immunological responses of K18-hACE2 mice to SARS-CoV-2 infection. Mice were treated with a combination of antibiotics (kanamycin, gentamicin, metronidazole, vancomycin, and colistin, Abx) for 3 days, and 24 h later, they were infected with SARS-CoV-2 B lineage. Here, we show that more than 80% of mice succumbed to infection by day 11 post-infection. Treatment with Abx had no impact on mortality. However, Abx-treated mice presented better clinical symptoms, with similar weight loss between infected–treated and non-treated groups. We observed no differences in lung and colon histopathological scores or lung, colon, heart, brain and kidney viral load between groups on day 5 of infection. Despite some minor differences in the expression of antiviral and inflammatory markers in the lungs and colon, no robust change was observed in Abx-treated mice. Together, these findings indicate that microbiota depletion has no impact on SARS-CoV-2 infection in mice.
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