Literature DB >> 14643407

Differentiation of Fonsecaea pedrosoi mycelial forms into sclerotic cells is induced by platelet-activating factor.

Daniela S Alviano1, Lucimar F Kneipp, Angela H Lopes, Luiz R Travassos, José R Meyer-Fernandes, Marcio L Rodrigues, Celuta S Alviano.   

Abstract

Platelet-activating factor (PAF) has been shown to induce the differentiation of several cell types. In this work, we evaluated the effects of PAF on the formation of sclerotic cells of Fonsecaea pedrosoi, the major causative agent of chromoblastomycosis. Cell differentiation was evaluated by light and electron microscopy, which showed that treatment of mycelial forms with PAF results in the generation of sclerotic bodies with typical morphological characteristics. Biochemical features of PAF-induced sclerotic cells were also analyzed and compared with those from sclerotic forms induced by propranolol, a previously described differentiating agent of F. pedrosoi. Chemical analyses of lipid and carbohydrate components from PAF- or propranolol-induced sclerotic bodies revealed that palmitic, stearic, oleic and linoleic acids were the major fatty acid components, while glucose, mannose, galactose and rhamnose were detected as the principal sugar constituents in these cells. Surface carbohydrate components of PAF- and propranolol-induced sclerotic cells were also evaluated, by flow cytometry analysis with twelve different lectins. The profile of reactivity of PAF- or propranolol-induced fungal cells with lectins was also very similar. Hydrolysis of the synthetic substrate p-nitrophenylphosphate by fungal cells demonstrated that the addition of PAF or propranolol to the mycelial cultures similarly promotes a significant increase in ecto-phosphatase activity. These results indicate that the differentiation of F. pedrosoi mycelial cells induced by PAF generates authentic sclerotic forms, as confirmed by the analysis of morphological and biochemical attributes. Since PAF is synthesized in normal conditions by the human host, these observations may have a correlation with the differentiation of F. pedrosoi in vivo.

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Year:  2003        PMID: 14643407     DOI: 10.1016/j.resmic.2003.09.002

Source DB:  PubMed          Journal:  Res Microbiol        ISSN: 0923-2508            Impact factor:   3.992


  10 in total

1.  Development of natural culture media for rapid induction of Fonsecaea pedrosoi sclerotic cells in vitro.

Authors:  Moises Batista da Silva; Jorge Pereira da Silva; Suellen Sirleide Pereira Yamano; Ubirajara Imbiriba Salgado; José Antonio Picanço Diniz; Claudio Guedes Salgado
Journal:  J Clin Microbiol       Date:  2008-09-17       Impact factor: 5.948

Review 2.  Black yeasts and their filamentous relatives: principles of pathogenesis and host defense.

Authors:  Seyedmojtaba Seyedmousavi; Mihai G Netea; Johan W Mouton; Willem J G Melchers; Paul E Verweij; G Sybren de Hoog
Journal:  Clin Microbiol Rev       Date:  2014-07       Impact factor: 26.132

3.  A case of relapsed chromoblastomycosis due to Fonsecaea monophora: antifungal susceptibility and phylogenetic analysis.

Authors:  Tatiane Caroline Daboit; Cibele Massotti Magagnin; Daiane Heidrich; Mauricio Ramírez Castrillón; Sandra Denise Camargo Mendes; Gerson Vettorato; Patrícia Valente; Maria Lúcia Scroferneker
Journal:  Mycopathologia       Date:  2013-05-04       Impact factor: 2.574

4.  Possible roles of ectophosphatases in host-parasite interactions.

Authors:  Marta T Gomes; Angela H Lopes; José Roberto Meyer-Fernandes
Journal:  J Parasitol Res       Date:  2011-04-26

Review 5.  Biochemical properties and possible roles of ectophosphatase activities in fungi.

Authors:  Anita Leocadio Freitas-Mesquita; José Roberto Meyer-Fernandes
Journal:  Int J Mol Sci       Date:  2014-02-06       Impact factor: 5.923

6.  Glycan analysis of Fonsecaea monophora from clinical and environmental origins reveals different structural profile and human antigenic response.

Authors:  Juliana R Burjack; Arquimedes P Santana-Filho; Andrea C Ruthes; Daniel S Riter; Vania A Vicente; Larissa M Alvarenga; Guilherme L Sassaki
Journal:  Front Cell Infect Microbiol       Date:  2014-10-31       Impact factor: 5.293

7.  Modulation of the immune response by Fonsecaea pedrosoi morphotypes in the course of experimental chromoblastomycosis and their role on inflammatory response chronicity.

Authors:  Isaque Medeiros Siqueira; Raffael Júnio Araújo de Castro; Luiza Chaves de Miranda Leonhardt; Márcio Sousa Jerônimo; Aluízio Carlos Soares; Tainá Raiol; Christiane Nishibe; Nalvo Almeida; Aldo Henrique Tavares; Christian Hoffmann; Anamelia Lorenzetti Bocca
Journal:  PLoS Negl Trop Dis       Date:  2017-03-29

8.  A chitin-like component on sclerotic cells of Fonsecaea pedrosoi inhibits Dectin-1-mediated murine Th17 development by masking β-glucans.

Authors:  Bilin Dong; Dongsheng Li; Ruoyu Li; Sharon C-A Chen; Weihuang Liu; Wei Liu; Liuqing Chen; Yao Chen; Xu Zhang; Zhongsheng Tong; Yun Xia; Ping Xia; Yan Wang; Yiqun Duan
Journal:  PLoS One       Date:  2014-12-09       Impact factor: 3.240

9.  Transformation of Fonsecaea pedrosoi into sclerotic cells links to the refractoriness of experimental chromoblastomycosis in BALB/c mice via a mechanism involving a chitin-induced impairment of IFN-γ production.

Authors:  Bilin Dong; Zhongsheng Tong; Ruoyu Li; Sharon C-A Chen; Weihuang Liu; Wei Liu; Yao Chen; Xu Zhang; Yiqun Duan; Dongsheng Li; Liuqing Chen
Journal:  PLoS Negl Trop Dis       Date:  2018-02-26

10.  Muriform Cells Can Reproduce by Dividing in an Athymic Murine Model of Chromoblastomycosis due to Fonsecaea pedrosoi.

Authors:  Bilin Dong; Wei Liu; Ruoyu Li; Yao Chen; Zhongsheng Tong; Xu Zhang; Liuqing Chen; Dongsheng Li
Journal:  Am J Trop Med Hyg       Date:  2020-06-04       Impact factor: 2.345

  10 in total

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