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Extracellular vesicles from paracoccidioides brasiliensis induced M1 polarization in vitro (2016)

  • Authors:
  • USP affiliated authors: BARREIRA, MARIA CRISTINA ROQUE ANTUNES - FMRP
  • USP Schools: FMRP
  • DOI: 10.1038/srep35867
  • Subjects: PARACOCCIDIOIDES BRASILIENSIS; VIRULÊNCIA; MACRÓFAGOS
  • Language: Inglês
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    Informações sobre o DOI: 10.1038/srep35867 (Fonte: oaDOI API)
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    Título do periódico: Scientific Reports

    ISSN: 2045-2322

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    Informações sobre o Citescore
  • Título: Scientific Reports

    ISSN: 2045-2322

    Citescore - 2017: 4.36

    SJR - 2017: 1.533

    SNIP - 2017: 1.245


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    • ABNT

      SILVA, Thiago Aparecido da; ROQUE-BARREIRA, Maria Cristina; CASADEVALL, Arturo; ALMEIDA, Fausto. Extracellular vesicles from paracoccidioides brasiliensis induced M1 polarization in vitro. Scientific Reports, London, v. 6, 2016. Disponível em: < http://dx.doi.org/10.1038/srep35867 > DOI: 10.1038/srep35867.
    • APA

      Silva, T. A. da, Roque-Barreira, M. C., Casadevall, A., & Almeida, F. (2016). Extracellular vesicles from paracoccidioides brasiliensis induced M1 polarization in vitro. Scientific Reports, 6. doi:10.1038/srep35867
    • NLM

      Silva TA da, Roque-Barreira MC, Casadevall A, Almeida F. Extracellular vesicles from paracoccidioides brasiliensis induced M1 polarization in vitro [Internet]. Scientific Reports. 2016 ; 6Available from: http://dx.doi.org/10.1038/srep35867
    • Vancouver

      Silva TA da, Roque-Barreira MC, Casadevall A, Almeida F. Extracellular vesicles from paracoccidioides brasiliensis induced M1 polarization in vitro [Internet]. Scientific Reports. 2016 ; 6Available from: http://dx.doi.org/10.1038/srep35867

    Referências citadas na obra
    Brummer, E., Castaneda, E. & Restrepo, A. Paracoccidioidomycosis: an update. Clin Microbiol Rev 6, 89–117 (1993).
    Restrepo, A., McEwen, J. G. & Castaneda, E. The habitat of Paracoccidioides brasiliensis: how far from solving the riddle? Med Mycol 39, 233–241 (2001).
    Teixeira, M. M. et al. Phylogenetic analysis reveals a high level of speciation in the Paracoccidioides genus. Molecular Phylogenetics and Evolution 52, 273–283, 10.1016/J.Ympev.2009.04.005 (2009).
    Laniado-Laborin, R. Coccidioidomycosis and other endemic mycoses in Mexico. Rev Iberoam Micol 24, 249–258, 200724249 [pii] (2007).
    de Almeida, S. M. Central nervous system paracoccidioidomycosis: an overview. Braz J Infect Dis 9, 126–133, S1413-86702005000200002 (2005).
    Restrepo, A. Morphological aspects of Paracoccidioides brasiliensis in lymph nodes: implications for the prolonged latency of paracoccidioidomycosis? Med Mycol 38, 317–322 (2000).
    Monod, M. & Borg-von Zepelin, M. Secreted proteinases and other virulence mechanisms of Candida albicans. Chem Immunol 81, 114–128 (2002).
    Batanghari, J. W., Deepe, G. S. Jr., Di Cera, E. & Goldman, W. E. Histoplasma acquisition of calcium and expression of CBP1 during intracellular parasitism. Mol Microbiol 27, 531–539 (1998).
    Vargas, G. et al. Compositional and immunobiological analyses of extracellular vesicles released by Candida albicans. Cell Microbiol 17, 389–407, 10.1111/cmi.12374 (2015).
    Glick, B. S. & Malhotra, V. The curious status of the Golgi apparatus. Cell 95, 883–889 (1998).
    Panepinto, J. et al. Sec6-dependent sorting of fungal extracellular exosomes and laccase of Cryptococcus neoformans. Mol Microbiol 71, 1165–1176, 10.1111/j.1365-2958.2008.06588.x (2009).
    Manjithaya, R., Anjard, C., Loomis, W. F. & Subramani, S. Unconventional secretion of Pichia pastoris Acb1 is dependent on GRASP protein, peroxisomal functions, and autophagosome formation. J Cell Biol 188, 537–546, 10.1083/jcb.200911149 (2010).
    Albuquerque, P. C. et al. Vesicular transport in Histoplasma capsulatum: an effective mechanism for trans-cell wall transfer of proteins and lipids in ascomycetes. Cell Microbiol 10, 1695–1710, 10.1111/j.1462-5822.2008.01160.x (2008).
    Rodrigues, M. L. et al. Extracellular vesicles produced by Cryptococcus neoformans contain protein components associated with virulence. Eukaryotic Cell 7, 58–67, 10.1128/Ec.00370-07 (2008).
    Oliveira, D. L. et al. Extracellular vesicles from Cryptococcus neoformans modulate macrophage functions. Infect Immun 78, 1601–1609, 10.1128/IAI.01171-09 (2010).
    Vallejo, M. C. et al. The pathogenic fungus Paracoccidioides brasiliensis exports extracellular vesicles containing highly immunogenic alpha-Galactosyl epitopes. Eukaryot Cell 10, 343–351, 10.1128/EC.00227-10 (2011).
    Vallejo, M. C. et al. Vesicle and vesicle-free extracellular proteome of Paracoccidioides brasiliensis: comparative analysis with other pathogenic fungi. J Proteome Res 11, 1676–1685, 10.1021/pr200872s (2012).
    Vallejo, M. C. et al. Lipidomic analysis of extracellular vesicles from the pathogenic phase of Paracoccidioides brasiliensis. PLoS One 7, e39463, 10.1371/journal.pone.0039463 (2012).
    da Silva, R. P. et al. Extracellular vesicle-mediated export of fungal RNA. Sci Rep 5, 7763, 10.1038/srep07763 (2015).
    Peres da Silva, R. et al. Extracellular vesicles from Paracoccidioides pathogenic species transport polysaccharide and expose ligands for DC-SIGN receptors. Sci Rep 5, 14213, 10.1038/srep14213 (2015).
    Bliska, J. B., Wang, X., Viboud, G. I. & Brodsky, I. E. Modulation of innate immune responses by Yersinia type III secretion system translocators and effectors. Cell Microbiol 15, 1622–1631, 10.1111/cmi.12164 (2013).
    Rana, R. R. et al. Yersinia pestis TIR-domain protein forms dimers that interact with the human adaptor protein MyD88. Microb Pathog 51, 89–95, 10.1016/j.micpath.2011.05.004 (2011).
    Eigenheer, R. A., Jin Lee, Y., Blumwald, E., Phinney, B. S. & Gelli, A. Extracellular glycosylphosphatidylinositol-anchored mannoproteins and proteases of Cryptococcus neoformans. FEMS Yeast Res 7, 499–510, 10.1111/j.1567-1364.2006.00198.x (2007).
    Almeida, F., Wolf, J. M. & Casadevall, A. Virulence-associated enzymes of Cryptococcus neoformans. Eukaryot Cell 14, 1173–1185, 10.1128/EC.00103-15 (2015).
    Beauvais, A. et al. Dipeptidyl-peptidase IV secreted by Aspergillus fumigatus, a fungus pathogenic to humans. Infect Immun 65, 3042–3047 (1997).
    Chaffin, W. L., Lopez-Ribot, J. L., Casanova, M., Gozalbo, D. & Martinez, J. P. Cell wall and secreted proteins of Candida albicans: identification, function, and expression. Microbiol Mol Biol Rev 62, 130–180 (1998).
    Djordjevic, J. T., Del Poeta, M., Sorrell, T. C., Turner, K. M. & Wright, L. C. Secretion of cryptococcal phospholipase B1 (PLB1) is regulated by a glycosylphosphatidylinositol (GPI) anchor. Biochemical Journal 389, 803–812, 10.1042/Bj20050063 (2005).
    Hussell, T. & Bell, T. J. Alveolar macrophages: plasticity in a tissue-specific context. Nat Rev Immunol 14, 81–93, 10.1038/nri3600 (2014).
    Murray, P. J. & Wynn, T. A. Protective and pathogenic functions of macrophage subsets. Nat Rev Immunol 11, 723–737, 10.1038/nri3073 (2011).
    de Carli, M. L. et al. M2 macrophages and inflammatory cells in oral lesions of chronic paracoccidioidomycosis. J Oral Pathol Med 45, 141–147, 10.1111/jop.12333 (2016).
    Costa, T. A. et al. In Pulmonary Paracoccidioidomycosis IL-10 Deficiency Leads to Increased Immunity and Regressive Infection without Enhancing Tissue Pathology. Plos Neglected Tropical Diseases 7, 10.1371/journal.pntd.0002512 (2013).
    Davis, M. J. et al. Macrophage M1/M2 polarization dynamically adapts to changes in cytokine microenvironments in Cryptococcus neoformans infection. MBio 4, e00264–00213, 10.1128/mBio.00264-13 (2013).
    Schorey, J. S., Cheng, Y., Singh, P. P. & Smith, V. L. Exosomes and other extracellular vesicles in host-pathogen interactions. EMBO Rep 16, 24–43, 10.15252/embr.201439363 (2015).
    Gehrmann, U. et al. Nanovesicles from Malassezia sympodialis and host exosomes induce cytokine responses–novel mechanisms for host-microbe interactions in atopic eczema. PLoS One 6, e21480, 10.1371/journal.pone.0021480 (2011).
    Lawrence, T. & Natoli, G. Transcriptional regulation of macrophage polarization: enabling diversity with identity. Nat Rev Immunol 11, 750–761, 10.1038/nri3088 (2011).
    Reales-Calderon, J. A., Aguilera-Montilla, N., Corbi, A. L., Molero, G. & Gil, C. Proteomic characterization of human proinflammatory M1 and anti-inflammatory M2 macrophages and their response to Candida albicans. Proteomics 14, 1503–1518, 10.1002/pmic.201300508 (2014).
    Hardison, S. E. et al. Pulmonary infection with an interferon-gamma-producing Cryptococcus neoformans strain results in classical macrophage activation and protection. Am J Pathol 176, 774–785, 10.2353/ajpath.2010.090634 (2010).
    Hardison, S. E., Wozniak, K. L., Kolls, J. K. & Wormley, F. L. Jr. Interleukin-17 is not required for classical macrophage activation in a pulmonary mouse model of Cryptococcus neoformans infection. Infect Immun 78, 5341–5351, 10.1128/IAI.00845-10 (2010).
    de Souza Silva, C. et al. The Effects of Paracoccidioides brasiliensis Infection on GM-CSF- and M-CSF-Induced Mouse Bone Marrow-Derived Macrophage from Resistant and Susceptible Mice Strains. Mediators Inflamm 2015, 605450, 10.1155/2015/605450 (2015).
    Feriotti, C., Loures, F. V., Frank de Araujo, E., da Costa, T. A. & Calich, V. L. Mannosyl-recognizing receptors induce an M1-like phenotype in macrophages of susceptible mice but an M2-like phenotype in mice resistant to a fungal infection. PLoS One 8, e54845, 10.1371/journal.pone.0054845 (2013).
    Pina, A., Bernardino, S. & Calich, V. L. Alveolar macrophages from susceptible mice are more competent than those of resistant mice to control initial Paracoccidioides brasiliensis infection. J Leukoc Biol 83, 1088–1099, 10.1189/jlb.1107738 (2008).
    Alegre-Maller, A. C. et al. Therapeutic administration of recombinant Paracoccin confers protection against paracoccidioides brasiliensis infection: involvement of TLRs. PLoS Negl Trop Dis 8, e3317, 10.1371/journal.pntd.0003317 (2014).
    Freitas, M. S. et al. Paracoccin Induces M1 Polarization of Macrophages via Interaction with TLR4. Front Microbiol 7, 1003, 10.3389/fmicb.2016.01003 (2016).
    Zheng, X. F. et al. Lipopolysaccharide-induced M2 to M1 macrophage transformation for IL-12p70 production is blocked by Candida albicans mediated up-regulation of EBI3 expression. PLoS One 8, e63967, 10.1371/journal.pone.0063967 (2013).
    Green, L. C. et al. Analysis of nitrate, nitrite, and [15N]nitrate in biological fluids. Anal Biochem 126, 131–138 (1982).
    Loures, F. V. et al. MyD88 signaling is required for efficient innate and adaptive immune responses to Paracoccidioides brasiliensis infection. Infect Immun 79, 2470–2480, 10.1128/IAI.00375-10 (2011).
    Alegre, A. C., Oliveira, A. F., Dos Reis Almeida, F. B., Roque-Barreira, M. C. & Hanna, E. S. Recombinant paracoccin reproduces the biological properties of the native protein and induces protective Th1 immunity against Paracoccidioides brasiliensis infection. PLoS Negl Trop Dis 8, e2788, 10.1371/journal.pntd.0002788 (2014).