Involvement of an Alternative Oxidase in Oxidative Stress and Mycelium-to-Yeast Differentiation in Paracoccidioides brasiliensis


Autoria(s): MARTINS, Vicente P.; DINAMARCO, Taisa M.; SORIANI, Frederico M.; TUDELLA, Valeria G.; OLIVEIRA, Sergio C.; GOLDMAN, Gustavo H.; CURTI, Carlos; UYEMURA, Sergio A.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2011

Resumo

Paracoccidioides brasiliensis is a thermodimorphic human pathogenic fungus that causes paracoccidioidomycosis (PCM), which is the most prevalent systemic mycosis in Latin America. Differentiation from the mycelial to the yeast form (M-to-Y) is an essential step for the establishment of PCM. We evaluated the involvement of mitochondria and intracellular oxidative stress in M-to-Y differentiation. M-to-Y transition was delayed by the inhibition of mitochondrial complexes III and IV or alternative oxidase (AOX) and was blocked by the association of AOX with complex III or IV inhibitors. The expression of P. brasiliensis aox (Pbaox) was developmentally regulated through M-to-Y differentiation, wherein the highest levels were achieved in the first 24 h and during the yeast exponential growth phase; Pbaox was upregulated by oxidative stress. Pbaox was cloned, and its heterologous expression conferred cyanide-resistant respiration in Saccharomyces cerevisiae and Escherichia coli and reduced oxidative stress in S. cerevisiae cells. These results reinforce the role of PbAOX in intracellular redox balancing and demonstrate its involvement, as well as that of other components of the mitochondrial respiratory chain complexes, in the early stages of the M-to-Y differentiation of P. brasiliensis.

FAPESP[99/04126-0]

CAPES[DS 103/00]

Identificador

EUKARYOTIC CELL, v.10, n.2, p.237-248, 2011

1535-9778

http://producao.usp.br/handle/BDPI/19979

10.1128/EC.00194-10

http://dx.doi.org/10.1128/EC.00194-10

Idioma(s)

eng

Publicador

AMER SOC MICROBIOLOGY

Relação

Eukaryotic Cell

Direitos

restrictedAccess

Copyright AMER SOC MICROBIOLOGY

Palavras-Chave #NADH-UBIQUINONE OXIDOREDUCTASES #HISTOPLASMA-CAPSULATUM #CANDIDA-ALBICANS #GLYOXYLATE CYCLE #MYCOBACTERIUM-TUBERCULOSIS #TRANSCRIPTOME ANALYSIS #ASPERGILLUS-FUMIGATUS #EXPRESSION ANALYSIS #MURINE MACROPHAGES #ELECTRON-TRANSPORT #Microbiology
Tipo

article

original article

publishedVersion