| Grant number: | 16/25167-3 |
| Support Opportunities: | Scholarships in Brazil - Master |
| Start date: | June 01, 2017 |
| End date: | May 31, 2019 |
| Field of knowledge: | Biological Sciences - Microbiology - Applied Microbiology |
| Agreement: | Coordination of Improvement of Higher Education Personnel (CAPES) |
| Principal Investigator: | Fausto Bruno dos Reis Almeida |
| Grantee: | Caroline Patini de Rezende |
| Host Institution: | Faculdade de Medicina de Ribeirão Preto (FMRP). Universidade de São Paulo (USP). Ribeirão Preto , SP, Brazil |
| Associated research grant: | 16/03322-7 - Role of galectin-3 in the Cryptococcus neoformans infection, AP.JP |
Abstract Cryptococcus neoformans is the causative agent of cryptococcosis and a major pathogen for immunosuppresed individuals. C. neoformans represents a unique model in cell biology studies since it is the only eukaryotic pathogen with a polysaccharide capsule. Futhermore, produces extracellular vesicles containing it major virulence factor. These vesicles cross the cell wall to reach the extracellular space, where the polysaccharide is supposedly used for capsule growth or delivered into host tissues. Galectin-3, a glycan-binding protein, control a broad spectrum of immunological functions, including cell adhesion, migration, activation, apoptosis and cytokine secretion within innate and adaptive immune compartments. Under the supervision of Dr. Arturo Casadevall in the Albert Einstein College of Medicine in New York, our group have verified that galectin-3 has lytic effect on extracellular vesicles of C. neoformans and we also have detected high serum levels of galectin-3 in the course of cryptococcosis murine experimental. These observations motivate the proposal to study the role of galectin-3 in the course of infection by C. neoformans. More specifically, we propose to do the following aims: (1) to compare the survival of C. neoformans infection between wild and knockout mice (galectin-3 KO), (2) to investigate the role of galectin-3 in the course of C. neoformans infection in mice through histhological and immunological parameters, (3) to analyze comparatively the gene profile of the host innate immune response during cryptococcosis, by real-time PCR arrangement (PCR Array), the modulation of genes related to response antifungal, as well as in addition to compare with the genic modulation of galectin-3 KO mice infected by C. neoformans. Our expectation is that galectin-3 may be responsible for important roles on the infection process by C. neoformans infection. (AU) | |
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