Abstract
Skin test-active, phenol-soluble, water-soluble (PSWS) extracts of Coccidioides immitis whole, defatted mycelia were compared with skin test-active, alkali-soluble, water-soluble (ASWS) extracts of mycelial cell walls. Both PSWS and ASWS extracts contained partially 3-O-methylated mannan. Composition analysis of both PSWS and ASWS extracts indicated mannose and glucose as major components, whereas 3-O-methylmannose and galactose were minor constituents. These heteromannans and glucans could be obtained from cell walls by extraction with either mild acid or alkali, but not with aqueous phenol. We therefore conclude that the PSWS extracts which were obtainable from whole mycelia but not from cell walls represent cellular (i.e., periplasmic, membrane associated, or cytoplasmic), nonwall polymers. Both PSWS and ASWS mycelial extracts and their gel filtration fractions reacted with rabbit antispherule serum, but with little cross-reactivity. However, alkali treatment of higher-molecular-weight PSWS extract polymers yielded products that cross-reacted with serological identity with low-molecular-weight components of ASWS extracts of mycelial walls, indicating that cell walls and cellular polymers share antigenic determinants. Finally, gel filtration of PSWS extracts on Sephacryl S-200 and Sepharose CL 4B yielded fractions that reacted with serological identity with one or more components of mycelial cytosol, mycelial culture filtrate and autolysate coccidioidins, and spherulin.
Full text
PDF






Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Anderson K. L., Wheat R. W., Conant N. F. Fractionation and composition studies of skin test-active components of sensitins from Coccidioides immitis. Appl Microbiol. 1971 Sep;22(3):294–299. doi: 10.1128/am.22.3.294-299.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bradford M. M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976 May 7;72:248–254. doi: 10.1016/0003-2697(76)90527-3. [DOI] [PubMed] [Google Scholar]
- Correa J. U., Elango N., Polacheck I., Cabib E. Endochitinase, a mannan-associated enzyme from Saccharomyces cerevisiae. J Biol Chem. 1982 Feb 10;257(3):1392–1397. [PubMed] [Google Scholar]
- Cox R. A., Mead C. G., Pavey E. F. Comparisons of mycelia- and spherule-derived antigens in cellular immune assays of Coccidioides immitis-infected guinea pigs. Infect Immun. 1981 Feb;31(2):687–692. doi: 10.1128/iai.31.2.687-692.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Drutz D. J., Catanzaro A. Coccidioidomycosis. Part I. Am Rev Respir Dis. 1978 Mar;117(3):559–585. doi: 10.1164/arrd.1978.117.3.559. [DOI] [PubMed] [Google Scholar]
- Elango N., Correa J. U., Cabib E. Secretory character of yeast chitinase. J Biol Chem. 1982 Feb 10;257(3):1398–1400. [PubMed] [Google Scholar]
- Gander J. E. Fungal cell wall glycoproteins and peptido-polysaccharides. Annu Rev Microbiol. 1974;28(0):103–119. doi: 10.1146/annurev.mi.28.100174.000535. [DOI] [PubMed] [Google Scholar]
- Landay M. E., Wheat R. W., Conant N. F., Lowe E. P. Serological comparison of the three morphological phases of Coccidioides immitis by the agar gel diffusion method. J Bacteriol. 1967 Jan;93(1):1–6. doi: 10.1128/jb.93.1.1-6.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Novick P., Schekman R. Secretion and cell-surface growth are blocked in a temperature-sensitive mutant of Saccharomyces cerevisiae. Proc Natl Acad Sci U S A. 1979 Apr;76(4):1858–1862. doi: 10.1073/pnas.76.4.1858. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Porter J. F., Scheer E. R., Wheat R. W. Characterization of 3-O-methylmannose from Coccidioides immitis. Infect Immun. 1971 Nov;4(5):660–661. doi: 10.1128/iai.4.5.660-661.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Raff R. A., Wheat R. W. Carbohydrate composition of the phenol-soluble lipopolysaccharides of Citrobacter freundii. J Bacteriol. 1968 Jun;95(6):2035–2043. doi: 10.1128/jb.95.6.2035-2043.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
- San-Blas G. The cell wall of fungal human pathogens: its possible role in host-parasite relationships. Mycopathologia. 1982 Sep 17;79(3):159–184. doi: 10.1007/BF01837196. [DOI] [PubMed] [Google Scholar]
- Ward E. R., Jr, Cox R. A., Schmitt J. A., Jr, Huppert M., Sun S. H. Delayed-type hypersensitivity responses to a cell wall fraction of the mycelial phase of Coccidioides immitis. Infect Immun. 1975 Nov;12(5):1093–1097. doi: 10.1128/iai.12.5.1093-1097.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wheat R. W., Su Chung K. S., Ornellas E. P., Scheer E. R. Extraction of skin test activity from Coccidioides immitis mycelia by water, perchloric acid, and aqueous phenol extraction. Infect Immun. 1978 Jan;19(1):152–159. doi: 10.1128/iai.19.1.152-159.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wheat R. W., Tritschler C., Conant N. F., Lowe E. P. Comparison of Coccidioides immitis arthrospore, mycelium, and spherule cell walls, and influence of growth medium on mycelial cell wall composition. Infect Immun. 1977 Jul;17(1):91–97. doi: 10.1128/iai.17.1.91-97.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wheat R., Scheer E. Cell walls of Coccidioides immitis: neutral sugars of aqueous alkaline extract polymers. Infect Immun. 1977 Jan;15(1):340–341. doi: 10.1128/iai.15.1.340-341.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]

