Exocellular proteolytic activity of Paracoccidioides brasiliensis: cleavage of components associated with the basement membrane

References

• San-Blas G, San-Blas F. Biochemistry of Paracoccidioides brasiliensis dimorphism. Paracoccidioidomycosis, M Franco, CS Lacaz, A Restrepo-Moreno, G Del Negro. CRC Press, Boca Raton, FL 1993; 49–66, In
   Google Scholar
• Puccia R, Travassos LR. 43-Kilodalton glycoprotein from Paracoccidioides brasiliensis: immunochemical reactions with sera from patients with paracoccidiodomycosis, histoplasmosis, and Jorge Lobo's disease. J Clin Microbiol 1991; 29: 1610–1615
   PubMed Web of Science ®Google Scholar
• Rodrigues EG, Travassos LR. Nature of the reactive epitopes in Paracoccidioides brasiliensis polysaccharide antigen. J Med Vet My col 1994; 32: 77–81
   PubMedGoogle Scholar
• Vicentini, AP, Gesztesi, JL, Franco, MF, et al. Binding of Paracoccidioides brasiliensis to laminin through surface glycoprotein gp43 leadsto enhancement of fungal pathogenegis. Infect Immun 1994; 62: 1465–1469
   PubMed Web of Science ®Google Scholar
• Carmona AK, Puccia R, Oliveira MCF, Rodrigues E, Juliano L, Travassos LR. Characterization of an exocellular serine-thiol proteinase activity in Paracoccidioides brasiliensis. Biochem J 1995; 309: 209–214
   PubMed Web of Science ®Google Scholar
• Stepanov, VM, Chestukhina, GG, Rudenskaya, GN, et al. A new subfamily of microbial serine proteinases? Structural similarities of Bacillus thuringiensis and Thermoactinomyces vulgaris extracellular serine proteinases. Biochem Biophys Res Commun 1981; 100: 1680–1687
   PubMed Web of Science ®Google Scholar
• Jany KD, Lederer G, Mayer B. Amino acid sequence of proteinase K from the mold Tritirachium album Limber. Proteinase K — a subtilisin-related enzyme with disulfide bonds. FEBS Lett 1986; 199: 139–144
   Web of Science ®Google Scholar
• De Camargo Z, Unterkircher C, Campoy SP, Travassos LR. Production of Paracoccidioides brasiliensis exoantigens for immunodiffusion tests. J Clin Microbiol 1988; 26: 2147–2157
   PubMed Web of Science ®Google Scholar
• San-Blas G, Sorais F, San-Blas F, Ruiz-Herrera J. Ornithine decarboxylase in Paracoccidioides brasiliensis. Arch Microbiol 1996; 165: 311–316
   PubMed Web of Science ®Google Scholar
• San-Blas G, San-Blas F, Sorais F, Moreno B, Ruiz-Herrera J. Polyamines in growth and dimorphism of Paracoccidioides brasiliensis. Arch Microbiol 1997; 166: 411–413
   Web of Science ®Google Scholar
• Laemmli UK. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 1970; 227: 680–685
   PubMed Web of Science ®Google Scholar
• Timpl, R, Rhode, H, Robey, PG, et al. Laminin — a glycoprotein from basement membranes. J Biol Chem 1979; 254: 9933–9937
   PubMed Web of Science ®Google Scholar
• Wewer U, Albrechtsen R, Manthorpe M, Varon S, Engvall E, Ruoslahti E. Human laminin isolated in a nearly intact, biologically active form from placenta by limited proteolysis. J Biol Chem 1983; 258: 12654–12660
   PubMed Web of Science ®Google Scholar
• Pierschbacher MD, Hayman EG, Ruoslahti E. Location of the cell attachment site in fibronectin with monoclonal antibodies and proteolytic fragments of the molecule. Cell 1981; 26: 259–267
   PubMed Web of Science ®Google Scholar
• Michelacci YM, Mourão PAS, Laredo J, Dietrich CP. Chondroitin sulfates and proteoglycans from normal and arthrosic human cartilage. Conn Tiss Res 1979; 7: 29–36
   PubMed Web of Science ®Google Scholar
• Sampaio LO, Bayliss MT, Hardingham TE, Muir H. Dermatan sulphate proteoglycan from human articular cartilage. Variation in its content with age and its structural comparison with a small chondroitin sulphate proteoglycan from pig laryngeal cartilage. Biochem J 1988; 254: 757–764
   PubMed Web of Science ®Google Scholar
• Rosenberg LC, Choi HU, Tang LH, Johnson TL, Pal S. Isolation of dermatan sulfate proteoglycans with mature bovine articular cartilages. J Biol Chem 1985; 260: 6304–6317
   PubMed Web of Science ®Google Scholar
• Montenegro MR, Franco M. Pathology. Paracoccidioidomycosis, M Franco, CS Lacaz, A Restrepo-Moreno, G Del Negro. CRC Press, Boca Raton, FL 1993; 131–150, In
   Google Scholar
• Tang CM, Cohen J, Krausz T, Van Noorden S, Holden DW. The alkaline protease of Aspergillus fumigatus is not a virulence determinant in two murine models of invasive pulmonary asper-gillosis. Infect Immun 1993; 61: 1650–1656
   PubMed Web of Science ®Google Scholar