Skip to main content
Journal of Clinical Microbiology logoLink to Journal of Clinical Microbiology
. 1989 Aug;27(8):1759–1766. doi: 10.1128/jcm.27.8.1759-1766.1989

Immunoaffinity isolation and partial characterization of the Coccidioides immitis antigen detected by the tube precipitin and immunodiffusion-tube precipitin tests.

B L Zimmer 1, D Pappagianis 1
PMCID: PMC267668  PMID: 2504775

Abstract

The antigen participating in the tube precipitin (TP) serologic test for coccidioidomycosis was isolated from mycelial-phase antigen (coccidioidin) by immunoaffinity and characterized by various analytical procedures. This was accomplished by first preparing the antigen-antibody precipitate by using antigen and human serum positive for TP (immunoglobulin M) antibody and then liberating the antigen by digestion with pronase. This protease destroyed the antibody and left the antigen intact as indicated by immunodiffusion-TP. The coccidioidal antigen was isolated from the proteolytic digest by using size exclusion chromatography. DEAE chromatography of this antigen yielded two fractions with immunodiffusion-TP reactivity which had average molecular sizes of 225 and 140 kilodaltons, respectively. The presence of carbohydrate and amino acids indicated that the antigen(s) is a glycopeptide. Compositional analysis showed that one fraction contained 3-O-methylmannose, mannose, and glucose in a ratio of 8:1.2:1, whereas the second fraction contained 3-O-methylmannose, mannose, glucose, and galactose in a ratio of 1:1:1:1. The amino acids glycine, alanine, serine, threonine, aspartic acid plus asparagine, and glutamic acid plus glutamine constituted 60 to 70% of the amino acids in both glycopeptides. Neither antigen could be detected entering the gel in sodium dodecyl sulfate-polyacrylamide gel electrophoresis. Lectin affinity provided evidence of a high-mannose asparagine-linked glycopeptide in the first peak and an asparagine-linked glycopeptide with a biantennary complex-type structure in the second peak.

Full text

PDF
1759

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. 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]
  2. Boykins R. A., Liu T. Y. Automatic analysis of neutral sugar components in glycoproteins and complex carbohydrates. J Biochem Biophys Methods. 1980 Jan-Feb;2(1):71–78. doi: 10.1016/0165-022x(80)90075-5. [DOI] [PubMed] [Google Scholar]
  3. Calhoun D. L., Osir E. O., Dugger K. O., Galgiani J. N., Law J. H. Humoral antibody responses to specific antigens of Coccidioides immitis. J Infect Dis. 1986 Aug;154(2):265–272. doi: 10.1093/infdis/154.2.265. [DOI] [PubMed] [Google Scholar]
  4. Cox R. A., Britt L. A. Isolation of a coccidioidin component that reacts with immunoglobulin M precipitin antibody. Infect Immun. 1986 Sep;53(3):449–453. doi: 10.1128/iai.53.3.449-453.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Honda S. High-performance liquid chromatography of mono- and oligosaccharides. Anal Biochem. 1984 Jul;140(1):1–47. doi: 10.1016/0003-2697(84)90130-1. [DOI] [PubMed] [Google Scholar]
  6. Kornfeld R., Kornfeld S. Assembly of asparagine-linked oligosaccharides. Annu Rev Biochem. 1985;54:631–664. doi: 10.1146/annurev.bi.54.070185.003215. [DOI] [PubMed] [Google Scholar]
  7. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  8. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  9. Merril C. R., Goldman D., Sedman S. A., Ebert M. H. Ultrasensitive stain for proteins in polyacrylamide gels shows regional variation in cerebrospinal fluid proteins. Science. 1981 Mar 27;211(4489):1437–1438. doi: 10.1126/science.6162199. [DOI] [PubMed] [Google Scholar]
  10. Nakajima T., Ballou C. E. Characterization of the carbohydrate fragments obtained from Saccharomyces cerevisiae mannan by alkaline degradation. J Biol Chem. 1974 Dec 10;249(23):7679–7684. [PubMed] [Google Scholar]
  11. Nakajima T., Ballou C. E. Structure of the linkage region between the polysaccharide and protein parts of Saccharomyces cerevisiae mannan. J Biol Chem. 1974 Dec 10;249(23):7685–7694. [PubMed] [Google Scholar]
  12. Osawa T., Tsuji T. Fractionation and structural assessment of oligosaccharides and glycopeptides by use of immobilized lectins. Annu Rev Biochem. 1987;56:21–42. doi: 10.1146/annurev.bi.56.070187.000321. [DOI] [PubMed] [Google Scholar]
  13. PAPPAGIANIS D., PUTMAN E. W., KOBAYASHI G. S. Polysaccharide of Coccidioides immitis. J Bacteriol. 1961 Nov;82:714–723. doi: 10.1128/jb.82.5.714-723.1961. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. 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]
  15. SMITH C. E., SAITO M. T., BEARD R. R., KEPP R. M., CLARK R. W., EDDIE B. U. Serological tests in the diagnosis and prognosis of coccidioidomycosis. Am J Hyg. 1950 Jul;52(1):1–21. doi: 10.1093/oxfordjournals.aje.a119404. [DOI] [PubMed] [Google Scholar]
  16. SMITH C. E., SAITO M. T., SIMONS S. A. Pattern of 39,500 serologic tests in coccidioidomycosis. J Am Med Assoc. 1956 Feb 18;160(7):546–552. doi: 10.1001/jama.1956.02960420026008. [DOI] [PubMed] [Google Scholar]
  17. Sawaki Y., Huppert M., Bailey J. W., Yagi Y. Patterns of human antibody reactions in coccidioidomycosis. J Bacteriol. 1966 Jan;91(1):422–427. doi: 10.1128/jb.91.1.422-427.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Scheer E., Terai T., Kulkarni S., Conant N. F., Wheat R. W., Lowe E. P. Unusual reducing sugar from Coccidioides immitis. J Bacteriol. 1970 Aug;103(2):525–526. doi: 10.1128/jb.103.2.525-526.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Seid R. C., Jr, Schneider H., Bondarew S., Boykins R. A. Quantitation of L-glycero-D-manno-heptose and 3-deoxy-D-manno-octulosonic acid in rough core lipopolysaccharides by partition chromatography. Anal Biochem. 1982 Aug;124(2):320–326. doi: 10.1016/0003-2697(82)90046-x. [DOI] [PubMed] [Google Scholar]
  20. TREVELYAN W. E., PROCTER D. P., HARRISON J. S. Detection of sugars on paper chromatograms. Nature. 1950 Sep 9;166(4219):444–445. doi: 10.1038/166444b0. [DOI] [PubMed] [Google Scholar]
  21. Towbin H., Staehelin T., Gordon J. Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. Proc Natl Acad Sci U S A. 1979 Sep;76(9):4350–4354. doi: 10.1073/pnas.76.9.4350. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. WOLFROM M. L., PATIN D. L., DELEDERKREMER R. M. THIN-LAYER CHROMATOGRAPHY ON MICROCRYSTALLINE CELLULOSE. J Chromatogr. 1965 Mar;17:488–494. doi: 10.1016/s0021-9673(00)99899-6. [DOI] [PubMed] [Google Scholar]
  23. Weiner M. H. Antigenemia detected in human coccidioidomycosis. J Clin Microbiol. 1983 Jul;18(1):136–142. doi: 10.1128/jcm.18.1.136-142.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. 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]
  25. Wheat R. W., Woodruff W. W., 3rd, Haltiwanger R. S. Occurrence of antigenic (species-specific?) partially 3-O-methylated heteromannans in cell wall and soluble cellular (nonwall) components of Coccidioides immitis mycelia. Infect Immun. 1983 Aug;41(2):728–734. doi: 10.1128/iai.41.2.728-734.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. 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]
  27. Zimmer B. L., Pappagianis D. Characterization of a soluble protein of Coccidiodes immitis with activity as an immunodiffusion-complement fixation antigen. J Clin Microbiol. 1988 Nov;26(11):2250–2256. doi: 10.1128/jcm.26.11.2250-2256.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Zimmer B. L., Pappagianis D. Comparison of immunoblot analyses of spherule-endospore-phase extracellular protein and mycelial-phase antigen of Coccidioides immitis. Infect Immun. 1986 Jul;53(1):64–70. doi: 10.1128/iai.53.1.64-70.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Journal of Clinical Microbiology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES