Saccharomyces cerevisiae expressing Gp43 protects mice against Paracoccidioides brasiliensis infection.
The dimorphic fungus Paracoccidioides brasiliensis is the etiological agent of paracoccidioidomycosis (PCM). It is believed that approximately 10 million people are infected with the fungus and approximately 2% will eventually develop the disease. Unlike viral and bacterial diseases, fungal diseases...
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2015-01-01
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doaj-8f3849d59e5e4304913943ba10b4b2bf2020-11-25T02:33:34ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01103e012020110.1371/journal.pone.0120201Saccharomyces cerevisiae expressing Gp43 protects mice against Paracoccidioides brasiliensis infection.Mariana Aprigio Assis-MarquesAline Ferreira OliveiraLuciana Pereira RuasThaila Fernanda dos ReisMaria Cristina Roque-BarreiraPaulo Sergio Rodrigues CoelhoThe dimorphic fungus Paracoccidioides brasiliensis is the etiological agent of paracoccidioidomycosis (PCM). It is believed that approximately 10 million people are infected with the fungus and approximately 2% will eventually develop the disease. Unlike viral and bacterial diseases, fungal diseases are the ones against which there is no commercially available vaccine. Saccharomyces cerevisiae may be a suitable vehicle for immunization against fungal infections, as they require the stimulation of different arms of the immune response. Here we evaluated the efficacy of immunizing mice against PCM by using S. cerevisiae yeast expressing gp43. When challenged by inoculation of P. brasiliensis yeasts, immunized animals showed a protective profile in three different assays. Their lung parenchyma was significantly preserved, exhibiting fewer granulomas with fewer fungal cells than found in non-immunized mice. Fungal burden was reduced in the lung and spleen of immunized mice, and both organs contained higher levels of IL-12 and IFN-γ compared to those of non-vaccinated mice, a finding that suggests the occurrence of Th1 immunity. Taken together, our results indicate that the recombinant yeast vaccine represents a new strategy to confer protection against PCM.http://europepmc.org/articles/PMC4366343?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Mariana Aprigio Assis-Marques Aline Ferreira Oliveira Luciana Pereira Ruas Thaila Fernanda dos Reis Maria Cristina Roque-Barreira Paulo Sergio Rodrigues Coelho |
spellingShingle |
Mariana Aprigio Assis-Marques Aline Ferreira Oliveira Luciana Pereira Ruas Thaila Fernanda dos Reis Maria Cristina Roque-Barreira Paulo Sergio Rodrigues Coelho Saccharomyces cerevisiae expressing Gp43 protects mice against Paracoccidioides brasiliensis infection. PLoS ONE |
author_facet |
Mariana Aprigio Assis-Marques Aline Ferreira Oliveira Luciana Pereira Ruas Thaila Fernanda dos Reis Maria Cristina Roque-Barreira Paulo Sergio Rodrigues Coelho |
author_sort |
Mariana Aprigio Assis-Marques |
title |
Saccharomyces cerevisiae expressing Gp43 protects mice against Paracoccidioides brasiliensis infection. |
title_short |
Saccharomyces cerevisiae expressing Gp43 protects mice against Paracoccidioides brasiliensis infection. |
title_full |
Saccharomyces cerevisiae expressing Gp43 protects mice against Paracoccidioides brasiliensis infection. |
title_fullStr |
Saccharomyces cerevisiae expressing Gp43 protects mice against Paracoccidioides brasiliensis infection. |
title_full_unstemmed |
Saccharomyces cerevisiae expressing Gp43 protects mice against Paracoccidioides brasiliensis infection. |
title_sort |
saccharomyces cerevisiae expressing gp43 protects mice against paracoccidioides brasiliensis infection. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2015-01-01 |
description |
The dimorphic fungus Paracoccidioides brasiliensis is the etiological agent of paracoccidioidomycosis (PCM). It is believed that approximately 10 million people are infected with the fungus and approximately 2% will eventually develop the disease. Unlike viral and bacterial diseases, fungal diseases are the ones against which there is no commercially available vaccine. Saccharomyces cerevisiae may be a suitable vehicle for immunization against fungal infections, as they require the stimulation of different arms of the immune response. Here we evaluated the efficacy of immunizing mice against PCM by using S. cerevisiae yeast expressing gp43. When challenged by inoculation of P. brasiliensis yeasts, immunized animals showed a protective profile in three different assays. Their lung parenchyma was significantly preserved, exhibiting fewer granulomas with fewer fungal cells than found in non-immunized mice. Fungal burden was reduced in the lung and spleen of immunized mice, and both organs contained higher levels of IL-12 and IFN-γ compared to those of non-vaccinated mice, a finding that suggests the occurrence of Th1 immunity. Taken together, our results indicate that the recombinant yeast vaccine represents a new strategy to confer protection against PCM. |
url |
http://europepmc.org/articles/PMC4366343?pdf=render |
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