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Generation of Fluorescent Protein Fusions in Candida Species
Published on: March 4, 2017
Moonlighting proteins induce protection in a mouse model against Candida species
César Luis Medrano-Díaz1, Arturo Vega-González2, Estela Ruiz-Baca3
1Departamento de Biología, División de Ciencias Naturales y Exactas, Campus Guanajuato, Universidad de Guanajuato, Noria Alta S/N, Col. Noria Alta, C.P. 36050, Guanajuato, Guanajuato, Mexico.
Abstract:
In recent years, C. albicans and C. glabrata have been identified as the main cause of candidemia and invasive candidiasis in hospitalized and immunocompromised patients. In order to colonize the human host, these fungi express several virulence factors such as the response to oxidative stress and the formation of biofilms. In the expression of these virulence factors, the cell wall of C. albicans and C. glabrata is of fundamental importance. As the outermost structure of the yeast, the cell wall is the first to come in contact with the reactive oxygen species (ROS) generated during the respiratory outbreak, and in the formation of biofilms, it is the first to adhere to organs or medical devices implanted in the human host. In both processes, several cell wall proteins (CWP) are required, since they promote attachment to human cells or abiotic surfaces, as well as to detoxify ROS. In our working group we have identified moonlighting CWP in response to oxidative stress as well as in the formation of biofilms. Having identified moonlighting CWP in Candida species in response to two virulence factors indicates that these proteins may possibly be immunodominant. The aim of the present work was to evaluate whether proteins of this type such as fructose-bisphosphate aldolase (Fba1), phosphoglycerate kinase (Pgk) and pyruvate kinase (Pk), could confer protection in a mouse model against C. albicans and C. glabrata. For this, recombinant proteins His6-Fba1, His6-Pgk and His6-Pk were constructed and used to immunize several groups of mice. The immunized mice were infected with C. albicans or C. glabrata, and subsequently the liver, spleen and kidney were extracted and the number of CFU was determined. Our results showed that Pk confers immunity to mice against C. albicans, while Fba1 to C. glabrata. This data allows us to conclude that the moonlighting CWP, Fba1 and Pk confer in vivo protection in a specific way against each species of Candida. This makes them promising candidates for developing specific vaccines against these pathogens.
Insights
Moonlighting cell wall proteins pyruvate kinase (Pk) and fructose-bisphosphate aldolase (Fba1) from Candida species provide specific protection against C. albicans and C. glabrata respectively in mice, suggesting potential for targeted vaccines.
Area of Science:
- Mycology
- Immunology
- Vaccine Development
Background:
- Candida species, particularly C. albicans and C. glabrata, are major causes of candidemia and invasive candidiasis in vulnerable patients.
- Fungal cell wall proteins (CWP) are crucial virulence factors, mediating host colonization through oxidative stress response and biofilm formation.
- Moonlighting CWPs, performing multiple functions including virulence, are potential targets for therapeutic intervention.
Purpose of the Study:
- To investigate the immunoprotective potential of moonlighting CWPs (fructose-bisphosphate aldolase [Fba1], phosphoglycerate kinase [Pgk], and pyruvate kinase [Pk]) against C. albicans and C. glabrata.
- To evaluate the species-specific protective efficacy of these proteins in a murine model.
Main Methods:
- Recombinant His-tagged proteins (His6-Fba1, His6-Pgk, His6-Pk) were constructed.
- Mice were immunized with these recombinant proteins.
- Immunized mice were challenged with C. albicans or C. glabrata, and fungal burden in liver, spleen, and kidney was quantified by colony-forming units (CFU).
Main Results:
- Pyruvate kinase (Pk) conferred significant immunity in mice against C. albicans infection.
- Fructose-bisphosphate aldolase (Fba1) provided protection against C. glabrata infection.
- Phosphoglycerate kinase (Pgk) did not show significant protective effects in this model.
Conclusions:
- Moonlighting CWPs Fba1 and Pk demonstrate species-specific in vivo protection against C. albicans and C. glabrata.
- These findings highlight Fba1 and Pk as promising candidates for the development of targeted vaccines against invasive candidiasis.
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