Macrophage interaction with paracoccidioides brasiliensis yeast cells modulates fungal metabolism and generates a response to oxidative stress

ABTRACT: Macrophages are key players during Paracoccidioides brasiliensis infection. However, the relative contribution of the fungal response to counteracting macrophage activity remains poorly understood. In this work, we evaluated the P. brasiliensis proteomic response to macrophage internalizati...

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Autores:
Parente Rocha, Juliana Alves
Alves Parente, Ana Flávia
Baeza, Lilian Cristiane
Caixeta Bonfim, Sheyla Maria Rondon
Hernández Ruiz, Orville
McEwen Ochoa, Juan Guillermo
Melo Bailão, Alexandre
Pelleschi Taborda, Carlos
Luiz Borges, Clayton
De Almeida Soares, Célia Maria
Tipo de recurso:
Article of investigation
Fecha de publicación:
2015
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/22107
Acceso en línea:
http://hdl.handle.net/10495/22107
Palabra clave:
Micosis
Mycoses
Paracoccidioidomicosis
Paracoccidioidomycosis
Infecciones bacterianas
Bacterial Infections
Estrés Oxidativo
Oxidative Stress
Gluconeogénesis
Paracoccidioides brasiliensis
Rights
openAccess
License
http://creativecommons.org/licenses/by/2.5/co/
Description
Summary:ABTRACT: Macrophages are key players during Paracoccidioides brasiliensis infection. However, the relative contribution of the fungal response to counteracting macrophage activity remains poorly understood. In this work, we evaluated the P. brasiliensis proteomic response to macrophage internalization. A total of 308 differentially expressed proteins were detected in P. brasiliensis during infection. The positively regulated proteins included those involved in alternative carbon metabolism, such as enzymes involved in gluconeogenesis, beta-oxidation of fatty acids and amino acids catabolism. The down-regulated proteins during P. brasiliensis internalization in macrophages included those related to glycolysis and protein synthesis. Proteins involved in the oxidative stress response in P. brasiliensis yeast cells were also up-regulated during macrophage infection, including superoxide dismutases (SOD), thioredoxins (THX) and cytochrome c peroxidase (CCP). Antisense knockdown mutants evaluated the importance of CCP during macrophage infection. The results suggested that CCP is involved in a complex system of protection against oxidative stress and that gene silencing of this component of the antioxidant system diminished the survival of P. brasiliensis in macrophages and in a murine model of infection.