A quantitative view of the morphological phases of Paracoccidioides brasiliensis using proteomics

Journal of Proteomics

Volumn 75, Issue 2, 2011, Pages 572-587

  Rezende, Tereza C V ^a,b   Borges, Clayton L ^a   Magalhães, Adriana D ^b   de Sousa, Marcelo Valle ^b   Ricart, Carlos A O ^b   Bailão, Alexandre M ^a   Soares, Célia M A ^a  

^a FEDERAL UNIVERSITY OF GOIÁS   (Brazil)

^b UNIVERSITY OF BRASILIA   (Brazil)

Author keywords

Morphological transition; Paracoccidioides brasiliensis; Proteomic analysis

Indexed keywords

FUNGAL PROTEIN; PROTEOME;

ARTICLE; CONTROLLED STUDY; FUNGAL METABOLISM; FUNGUS GROWTH; MYCELIUM; NONHUMAN; PARACOCCIDIOIDES BRASILIENSIS; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN EXPRESSION; PROTEOMICS;

FUNGAL PROTEINS; MYCELIUM; PARACOCCIDIOIDES; PROTEOME; PROTEOMICS; SPECTROMETRY, MASS, MATRIX-ASSISTED LASER DESORPTION-IONIZATION; SPORES, FUNGAL; YEASTS;

PARACOCCIDIOIDES BRASILIENSIS;

EID: 82355192281     PISSN: 18743919     EISSN: 18767737     Source Type: Journal    
DOI: 10.1016/j.jprot.2011.08.020     Document Type: Article

References (34)

1. McEwen J.G., Bedoya V., Patino M.M., Salazar M.E., Restrepo A. Experimental murine paracoccidiodomycosis induced by the inhalation of conidia. J Med Vet Mycol 1987, 25(3):165-175.
2. Restrepo A., McEwen J.G., Castaneda E. The habitat of Paracoccidioides brasiliensis: how far from solving the riddle?. Med Mycol 2001, 39(3):233-241.
3. Brummer E., Castaneda E., Restrepo A. Paracoccidioidomycosis: an update. Clin Microbiol Rev 1993, 6(2):89-117.
4. Rooney P.J., Klein B.S. Linking fungal morphogenesis with virulence. Cell Microbiol 2002, 4(3):127-137.
5. Felipe M.S., Andrade R.V., Arraes F.B., Nicola A.M., Maranhao A.Q., Torres F.A., et al. Transcriptional profiles of the human pathogenic fungus Paracoccidioides brasiliensis in mycelium and yeast cells. J Biol Chem 2005, 280(26):24706-24714.
6. Nunes L.R., Costa de Oliveira R., Leite D.B., da Silva V.S., dos Reis Marques E., da Silva Ferreira M.E., et al. Transcriptome analysis of Paracoccidioides brasiliensis cells undergoing mycelium-to-yeast transition. Eukaryot Cell 2005, 4(12):2115-2128.
7. Bastos K.P., Bailao A.M., Borges C.L., Faria F.P., Felipe M.S., Silva M.G., et al. The transcriptome analysis of early morphogenesis in Paracoccidioides brasiliensis mycelium reveals novel and induced genes potentially associated to the dimorphic process. BMC Microbiol 2007, 7:29.
8. Fonseca C.A., Jesuino R.S., Felipe M.S., Cunha D.A., Brito W.A., Soares C.M.A. Two-dimensional electrophoresis and characterization of antigens from Paracoccidioides brasiliensis. Microbes Infect 2001, 3(7):535-542.
9. Nogueira S.V., Fonseca F.L., Rodrigues M.L., Mundodi V., Abi-Chacra E.A., Winters M.S., et al. Paracoccidioides brasiliensis enolase is a surface protein that binds plasminogen and mediates interaction of yeast forms with host cells. Infect Immun 2010, 78(9):4040-4050.
10. Borges C.L., Parente J.A., Barbosa M.S., Santana J.M., Bao S.N., de Sousa M.V., et al. Detection of a homotetrameric structure and protein-protein interactions of Paracoccidioides brasiliensis formamidase lead to new functional insights. FEMS Yeast Res 2010, 10(1).
11. Restrepo A., Salazar M.E., Cano L.E., Patino M.M. A technique to collect and dislodge conidia produced by Paracoccidioides brasiliensis mycelial form. J Med Vet Mycol 1986, 24(3):247-250.
12. Guercio R.A., Shevchenko A., Lopez-Lozano J.L., Paba J., Sousa M.V., Ricart C.A. Ontogenetic variations in the venom proteome of the Amazonian snake Bothrops atrox. Proteome Sci 2006, 4:11.
13. Shevchenko A., Wilm M., Vorm O., Mann M. Mass spectrometric sequencing of proteins silver-stained polyacrylamide gels. Anal Chem 1996, 68(5):850-858.
14. Winters M.S., Spellman D.S., Chan Q., Gomez F.J., Hernandez M., Catron B., et al. Histoplasma capsulatum proteome response to decreased iron availability. Proteome Sci 2008, 6:36.
15. Borges C.L., Bailao A.M., Bao S.N., Pereira M., Parente J.A., Soares C.M.A. Genes potentially relevant in the parasitic phase of the fungal pathogen Paracoccidioides brasiliensis. Mycopathologia 2011, 171(1):1-9.
16. Bookout A.L., Cummins C.L., Mangelsdorf D.J., Pesola J.M., Kramer M.F. High-throughput real-time quantitative reverse transcription PCR. Current Protocols in Molecular Biology 2006, 1581-1628. John Wiley and Sons, Hoboken NJ. F.M. Ausubel, R. Brent, R.E. Kingston, D.D. Moore, J.G. Seidman, J.A. Smith (Eds.).
17. Laemmli U.K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 1970, 227(5259):680-685.
18. Brito W.A., Rezende T.C.V., Parente A.F., Ricart C.A., Souza M.V., Bao S.N., et al. Identification, characterization and regulation studies of the Aconitase of Paracoccidioides brasiliensis. Fungal Biol 2011, 115(8):697-707.
19. Pereira L.A., Bao S.N., Barbosa M.S., da Silva J.L., Felipe M.S., de Santana J.M., et al. Analysis of the Paracoccidioides brasiliensis triosephosphate isomerase suggests the potential for adhesin function. FEMS Yeast Res 2007, 7(8):1381-1388.
20. Luk E., Yang M., Jensen L.T., Bourbonnais Y., Culotta V.C. Manganese activation of superoxide dismutase 2 in the mitochondria of Saccharomyces cerevisiae. J Biol Chem 2005, 280(24):22715-22720.
21. Chae H.Z., Robison K., Poole L.B., Church G., Storz G., Rhee S.G. Cloning and sequencing of thiol-specific antioxidant from mammalian brain: alkyl hydroperoxide reductase and thiol-specific antioxidant define a large family of antioxidant enzymes. Proc Natl Acad Sci USA 1994, 91(15):7017-7021.
22. Pedrajas J.R., Carreras A., Valderrama R., Barroso J.B. Mitochondrial 1-Cys-peroxiredoxin/thioredoxin system protects manganese-containing superoxide dismutase (Mn-SOD) against inactivation by peroxynitrite in Saccharomyces cerevisiae. Nitric Oxide 2010, 23(3):206-213.
23. Monteoliva L., Martinez-Lopez R., Pitarch A., Hernaez M.L., Serna A., Nombela C., et al. Quantitative proteome and acidic subproteome profiling of Candida albicans yeast-to-hypha transition. J Proteome Res 2011, 10(2):502-517.
24. Rui B., Shen T., Zhou H., Liu J., Chen J., Pan X., et al. A systematic investigation of Escherichia coli central carbon metabolism in response to superoxide stress. BMC Syst Biol 2010, 4:122.
25. Lorenz M.C., Fink G.R. The glyoxylate cycle is required for fungal virulence. Nature 2001, 412(6842):83-86.
26. Lorenz M.C., Fink G.R. Life and death in a macrophage: role of the glyoxylate cycle in virulence. Eukaryot Cell 2002, 1(5):657-662.
27. Munoz-Elias E.J., Upton A.M., Cherian J., McKinney J.D. Role of the methylcitrate cycle in Mycobacterium tuberculosis metabolism, intracellular growth, and virulence. Mol Microbiol 2006, 60(5):1109-1122.
28. Maresca B., Lambowitz A.M., Kumar V.B., Grant G.A., Kobayashi G.S., Medoff G. Role of cysteine in regulating morphogenesis and mitochondrial activity in the dimorphic fungus Histoplasma capsulatum. Proc Natl Acad Sci USA 1981, 78(7):4596-4600.
29. Medoff G., Painter A., Kobayashi G.S. Mycelial- to yeast-phase transitions of the dimorphic fungi Blastomyces dermatitidis and Paracoccidioides brasiliensis. J Bacteriol 1987, 169(9):4055-4060.
30. Zhu K., Zhao J., Lubman D.M., Miller F.R., Barder T.J. Protein pI shifts due to posttranslational modifications in the separation and characterization of proteins. Anal Chem 2005, 77(9):2745-2755.
31. Pal-Bhowmick I., Vora H.K., Jarori G.K. Sub-cellular localization and post-translational modifications of the Plasmodium yoelii enolase suggest moonlighting functions. Malar J 2007, 6:45.
32. Barbosa M.S., Bao S.N., Andreotti P.F., de Faria F.P., Felipe M.S., Feitosa L.S., et al. Glyceraldehyde-3-phosphate dehydrogenase of Paracoccidioides brasiliensis is a cell surface protein involved in fungal adhesion to extracellular matrix proteins and interaction with cells. Infect Immun 2006, 74(1):382-389.
33. Daher B.S., Venancio E.J., de Freitas S.M., Bao S.N., Vianney P.V., Andrade R.V., et al. The highly expressed yeast gene PbY20 from Paracoccidioides brasiliensis encodes a flavodoxin-like protein. Fungal Genet Biol 2005, 42(5):434-443.
34. Barbosa M.S., Cunha Passos D.A., Felipe M.S., Jesuino R.S., Pereira M., Soares C.M.A. The glyceraldehyde-3-phosphate dehydrogenase homologue is differentially regulated in phases of Paracoccidioides brasiliensis: molecular and phylogenetic analysis. Fungal Genet Biol 2004, 41(7):667-675.