Hemoglobin uptake by Paracoccidioides spp. is receptor-mediated

ABSTRACT: Iron is essential for the proliferation of fungal pathogens during infection. The availability of iron is limited due to its association with host proteins. Fungal pathogens have evolved different mechanisms to acquire iron from host; however, little is known regarding how Paracoccidioides species incorporate and metabolize this ion. In this work, host iron sources that are used by Paracoccidioides spp. were investigated. Robust fungal growth in the presence of the iron-containing molecules hemin and hemoglobin was observed. Paracoccidioides spp. present hemolytic activity and have the ability to internalize a protoporphyrin ring. Using real-time PCR and nanoUPLC-MSE proteomic approaches, fungal growth in the presence of hemoglobin was shown to result in the positive regulation of transcripts that encode putative hemoglobin receptors, in addition to the induction of proteins that are required for amino acid metabolism and vacuolar protein degradation. In fact, one hemoglobin receptor ortholog, Rbt5, was identified as a surface GPI-anchored protein that recognized hemin, protoporphyrin and hemoglobin in vitro. Antisense RNA technology and Agrobacterium tumefaciens-mediated transformation were used to generate mitotically stable Pbrbt5 mutants. The knockdown strain had a lower survival inside macrophages and in mouse spleen when compared with the parental strain, which suggested that Rbt5 could act as a virulence factor. In summary, our data indicate that Paracoccidioides spp. can use hemoglobin as an iron source most likely through receptor-mediated pathways that might be relevant for pathogenic mechanisms. Author Summary: Fungal infections contribute substantially to human morbidity and mortality. During infectious processes, fungi have evolved mechanisms to obtain iron from high-affinity iron-binding proteins. In the current study, we demonstrated that hemoglobin is the preferential host iron source for the thermodimorphic fungus Paracoccidioides spp. To acquire hemoglobin, the fungus presents hemolytic activity and the ability to internalize protoporphyrin rings. A putative hemoglobin receptor, Rbt5, was demonstrated to be GPI-anchored at the yeast cell surface. Rbt5 was able to bind to hemin, protoporphyrin and hemoglobin in vitro. When rbt5 expression was inhibited, the survival of Paracoccidioides sp. inside macrophages and the fungal burden in mouse spleen diminished, which indicated that Rbt5 could participate in the establishment of the fungus inside the host. Drugs or vaccines could be developed against Paracoccidioides spp. Rbt5 to disturb iron uptake of this micronutrient and, thus, the proliferation of the fungus. Moreover, this protein could be used in routes to introduce antifungal agents into fungal cells.

• Autores: Cardoso Bailao, Elisa Flavia Luiz; Alves Parente, Juliana; Lacerda Pigosso, Laurine; Pacheco De Castro, Kelly; Lopes Fonseca, Fernanda; Silva Bailao, Mirelle Garcia; Nair Bao, Sonia; Melo Bailao, Alexandre; L Rodrigues, Marcio; Hernandez Ruiz, Orville; McEwen Ochoa, Juan Guillermo; De Almeida Soares, Celia Maria
• Tipo de recurso: Article of investigation
• Fecha de publicación: 2014
• Institución: Universidad de Antioquia
• Repositorio: Repositorio UdeA
• Idioma: eng
• OAI Identifier: oai:bibliotecadigital.udea.edu.co:10495/38913
• Acceso en línea: https://hdl.handle.net/10495/38913
• Palabra clave: Línea Celular; Cell Line; Eritrocitos; Erythrocytes; Proteínas Fúngicas; Fungal Proteins; Hemo - metabolisimo; Heme - metabolism; Hemoglobinas - metabolisimo; Hemoglobins - metabolism; Hemólisis; Hemolysis; Hierro - metabolisimo; Iron - metabolism; Proteínas de Unión a Hierro; Iron-Binding Proteins; Paracoccidioides; Receptores de Superficie Celular; Receptors, Cell Surface; https://id.nlm.nih.gov/mesh/D002460; https://id.nlm.nih.gov/mesh/D004912; https://id.nlm.nih.gov/mesh/D005656; https://id.nlm.nih.gov/mesh/D006418; https://id.nlm.nih.gov/mesh/D006454; https://id.nlm.nih.gov/mesh/D006461; https://id.nlm.nih.gov/mesh/D007501; https://id.nlm.nih.gov/mesh/D033862; https://id.nlm.nih.gov/mesh/D010228; https://id.nlm.nih.gov/mesh/D011956
• Rights: openAccess
• License: http://creativecommons.org/licenses/by/2.5/co/