Aspectos relevantes del marcador molecular Hcp100 de Histoplasma capsulatum y su potencial uso terapéutico en la histoplasmosis

Antonio Ernesto González-González, Maria Lucia Taylor, Everardo Curiel-Quesada

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

3 Citas (Scopus)

Resumen

Background: Fungal pathogens have developed strategies, involving genes expression that favors their persistence and multiplication in the host. The absence of molecules encoded by these genes could interfere with the growth and death of these fungi. In the past, a coactivator protein coding gene . (Hcp100) of the fungus . Histoplasma capsulatum was reported, which is overexpressed after 1. h of contact between fungal yeast-cells and murine macrophages. The product of this gene, a protein of 100. kDa (Hcp100) of . H. capsulatum, is probably a regulatory protein involved in the processes required for fungal adaptation and its survival in the intracellular hostile conditions of the macrophages. A 210-bp fragment of the . Hcp100 marker has proved to be an excellent tool for . H. capsulatum molecular detection in clinical samples. The potential use of this gene as a therapeutic target in . Plasmodium falciparum has been explored through the inhibition of both, the gene and the protein p100 of the parasite, by blocking its growth. Methods: Based on the above mentioned antecedents, we believe that the Hcp100 has an important role in the development and maintenance of the . H. capsulatum yeast cells within macrophages. Results and conclusions: To study the probable function of Hcp100 in the yeast-phase of this fungal pathogen is relevant to understand its activity and to propose it as a therapeutic target for histoplasmosis treatment.

Título traducido de la contribuciónRelevant aspects of the Hcp100 molecular marker of Histoplasma capsulatum and its potential therapeutic use in histoplasmosis
Idioma originalEstonio
Páginas (desde-hasta)115-119
Número de páginas5
PublicaciónRevista Iberoamericana de Micologia
Volumen29
N.º3
DOI
EstadoPublicada - jul. 2012

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