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Pulmonary Fibrosis and Hypereosinophilia in TLR9 -/- Mice Infected by Cryptococcus gattii.

Authors :
da Silva-Junior, Elias Barbosa
Diniz-Lima, Israel
Silva, Amanda Couto
GuimarĂ£es-de-Oliveira, Joyce Cristina
Morrot, Alexandre
Freire-de-Lima, Leonardo
da Fonseca, Leonardo Marques
de Brito-Gitirana, Lycia
Decote-Ricardo, Debora
de Matos Guedes, Herbert Leonel
Freire-de-Lima, Celio Geraldo
Source :
Pathogens; Sep2022, Vol. 11 Issue 9, pN.PAG-N.PAG, 14p
Publication Year :
2022

Abstract

Cryptococcus gattii is a worldwide-distributed basidiomycetous yeast that can infect immunocompetent hosts. However, little is known about the mechanisms involved in the disease. The innate immune response is essential to the control of infections by microorganisms. Toll-like receptor 9 (TLR9) is an innate immune receptor, classically described as a non-methylated DNA recognizer and associated with bacteria, protozoa and opportunistic mycosis infection models. Previously, our group showed that TLR9<superscript>-/-</superscript> mice were more susceptible to C. gattii after 21 days of infection. However, some questions about the innate immunity involving TLR9 response against C. gattii remain unknown. In order to investigate the systemic cryptococcal infection, we evaluated C57BL/6 mice and C57BL/6 TLR9<superscript>-/-</superscript> after intratracheal infection with 10<superscript>4</superscript>C. gattii yeasts for 21 days. Our data evidenced that TLR9<superscript>-/-</superscript> was more susceptible to C. gattii. TLR9<superscript>-/-</superscript> mice had hypereosinophilia in pulmonary mixed cellular infiltrate, severe bronchiolitis and vasculitis and type 2 alveolar cell hyperplasia. In addition, TLR9<superscript>-/-</superscript> mice developed severe pulmonary fibrosis and areas with strongly birefringent fibers. Together, our results corroborate the hypothesis that TLR9 is important to support the Th1/Th17 response against C. gattii infection in the murine experimental model. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20760817
Volume :
11
Issue :
9
Database :
Complementary Index
Journal :
Pathogens
Publication Type :
Academic Journal
Accession number :
159334912
Full Text :
https://doi.org/10.3390/pathogens11090987