• 作者：Antonio Ernesto Gonzá ; lez-Gonzá ; lez^a ; ^{skapunking_9@yahoo.com.mx} ; Maria Lucia Taylor^a ; Everardo Curiel-Quesada^b
• 关键词：Gen Hcp100 ; Blanco terapé ; utico ; Proteí ; na coactivadora
• 刊名：Revista Iberoamericana de Micolog铆a
• 出版年：2012
• 期刊代码：pca320_11301406
• 类别：med
• 出版时间：July-September, 2012
• 卷：29
• 期：3
• 页码：115-119
• 文件大小：310 K

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.