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Impact of Microbiota Depletion by Antibiotics on SARS-CoV-2 Infection of K18-hACE2 Mice

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 thi...

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Detalles Bibliográficos
Autores principales: Rodrigues, Patrícia Brito, Gomes, Giovanni Freitas, Angelim, Monara K. S. C., Souza, Gabriela F., Muraro, Stefanie Primon, Toledo-Teixeira, Daniel A., Rattis, Bruna Amanda Cruz, Passos, Amanda Stephane, Pral, Laís Passarielo, de Rezende Rodovalho, Vinícius, dos Santos P. Gomes, Arilson Bernardo, Matheus, Valquíria Aparecida, Antunes, André Saraiva Leão Marcelo, Crunfli, Fernanda, Antunes, Krist Helen, de Souza, Ana Paula Duarte, Consonni, Sílvio Roberto, Leiria, Luiz Osório, Alves-Filho, José Carlos, Cunha, Thiago M., Moraes-Vieira, Pedro M. M., Proença-Módena, José Luiz, R. Vinolo, Marco Aurélio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9406363/
https://www.ncbi.nlm.nih.gov/pubmed/36010648
http://dx.doi.org/10.3390/cells11162572
Descripción
Sumario: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.