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Alternative Oxidase Mediates Pathogen Resistance in Paracoccidioides brasiliensis Infection

BACKGROUND: Paracoccidioides brasiliensis is a human thermal dimorphic pathogenic fungus. Survival of P. brasiliensis inside the host depends on the adaptation of this fungal pathogen to different conditions, namely oxidative stress imposed by immune cells. AIMS AND METHODOLOGY: In this study, we ev...

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Autores principales: Hernández Ruiz, Orville, Gonzalez, Angel, Almeida, Agostinho J., Tamayo, Diana, Garcia, Ana Maria, Restrepo, Angela, McEwen, Juan G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3201906/
https://www.ncbi.nlm.nih.gov/pubmed/22039556
http://dx.doi.org/10.1371/journal.pntd.0001353
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author Hernández Ruiz, Orville
Gonzalez, Angel
Almeida, Agostinho J.
Tamayo, Diana
Garcia, Ana Maria
Restrepo, Angela
McEwen, Juan G.
author_facet Hernández Ruiz, Orville
Gonzalez, Angel
Almeida, Agostinho J.
Tamayo, Diana
Garcia, Ana Maria
Restrepo, Angela
McEwen, Juan G.
author_sort Hernández Ruiz, Orville
collection PubMed
description BACKGROUND: Paracoccidioides brasiliensis is a human thermal dimorphic pathogenic fungus. Survival of P. brasiliensis inside the host depends on the adaptation of this fungal pathogen to different conditions, namely oxidative stress imposed by immune cells. AIMS AND METHODOLOGY: In this study, we evaluated the role of alternative oxidase (AOX), an enzyme involved in the intracellular redox balancing, during host-P. brasiliensis interaction. We generated a mitotically stable P. brasiliensis AOX (PbAOX) antisense RNA (aRNA) strain with a 70% reduction in gene expression. We evaluated the relevance of PbAOX during interaction of conidia and yeast cells with IFN-γ activated alveolar macrophages and in a mouse model of infection. Additionally, we determined the fungal cell's viability and PbAOX in the presence of H(2)O(2). RESULTS: Interaction with IFN-γ activated alveolar macrophages induced higher levels of PbAOX gene expression in PbWt conidia than PbWt yeast cells. PbAOX-aRNA conidia and yeast cells had decreased viability after interaction with macrophages. Moreover, in a mouse model of infection, we showed that absence of wild-type levels of PbAOX in P. brasiliensis results in a reduced fungal burden in lungs at weeks 8 and 24 post-challenge and an increased survival rate. In the presence of H(2)O(2), we observed that PbWt yeast cells increased PbAOX expression and presented a higher viability in comparison with PbAOX-aRNA yeast cells. CONCLUSIONS: These data further support the hypothesis that PbAOX is important in the fungal defense against oxidative stress imposed by immune cells and is relevant in the virulence of P. brasiliensis.
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spelling pubmed-32019062011-10-28 Alternative Oxidase Mediates Pathogen Resistance in Paracoccidioides brasiliensis Infection Hernández Ruiz, Orville Gonzalez, Angel Almeida, Agostinho J. Tamayo, Diana Garcia, Ana Maria Restrepo, Angela McEwen, Juan G. PLoS Negl Trop Dis Research Article BACKGROUND: Paracoccidioides brasiliensis is a human thermal dimorphic pathogenic fungus. Survival of P. brasiliensis inside the host depends on the adaptation of this fungal pathogen to different conditions, namely oxidative stress imposed by immune cells. AIMS AND METHODOLOGY: In this study, we evaluated the role of alternative oxidase (AOX), an enzyme involved in the intracellular redox balancing, during host-P. brasiliensis interaction. We generated a mitotically stable P. brasiliensis AOX (PbAOX) antisense RNA (aRNA) strain with a 70% reduction in gene expression. We evaluated the relevance of PbAOX during interaction of conidia and yeast cells with IFN-γ activated alveolar macrophages and in a mouse model of infection. Additionally, we determined the fungal cell's viability and PbAOX in the presence of H(2)O(2). RESULTS: Interaction with IFN-γ activated alveolar macrophages induced higher levels of PbAOX gene expression in PbWt conidia than PbWt yeast cells. PbAOX-aRNA conidia and yeast cells had decreased viability after interaction with macrophages. Moreover, in a mouse model of infection, we showed that absence of wild-type levels of PbAOX in P. brasiliensis results in a reduced fungal burden in lungs at weeks 8 and 24 post-challenge and an increased survival rate. In the presence of H(2)O(2), we observed that PbWt yeast cells increased PbAOX expression and presented a higher viability in comparison with PbAOX-aRNA yeast cells. CONCLUSIONS: These data further support the hypothesis that PbAOX is important in the fungal defense against oxidative stress imposed by immune cells and is relevant in the virulence of P. brasiliensis. Public Library of Science 2011-10-25 /pmc/articles/PMC3201906/ /pubmed/22039556 http://dx.doi.org/10.1371/journal.pntd.0001353 Text en Hernandez Ruiz et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Hernández Ruiz, Orville
Gonzalez, Angel
Almeida, Agostinho J.
Tamayo, Diana
Garcia, Ana Maria
Restrepo, Angela
McEwen, Juan G.
Alternative Oxidase Mediates Pathogen Resistance in Paracoccidioides brasiliensis Infection
title Alternative Oxidase Mediates Pathogen Resistance in Paracoccidioides brasiliensis Infection
title_full Alternative Oxidase Mediates Pathogen Resistance in Paracoccidioides brasiliensis Infection
title_fullStr Alternative Oxidase Mediates Pathogen Resistance in Paracoccidioides brasiliensis Infection
title_full_unstemmed Alternative Oxidase Mediates Pathogen Resistance in Paracoccidioides brasiliensis Infection
title_short Alternative Oxidase Mediates Pathogen Resistance in Paracoccidioides brasiliensis Infection
title_sort alternative oxidase mediates pathogen resistance in paracoccidioides brasiliensis infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3201906/
https://www.ncbi.nlm.nih.gov/pubmed/22039556
http://dx.doi.org/10.1371/journal.pntd.0001353
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