Skip to main content
Applied and Environmental Microbiology logoLink to Applied and Environmental Microbiology
. 1996 Sep;62(9):3176–3182. doi: 10.1128/aem.62.9.3176-3182.1996

Measurement of beta(1-->3)-glucans in occupational and home environments with an inhibition enzyme immunoassay.

J Douwes 1, G Doekes 1, R Montijn 1, D Heederik 1, B Brunekreef 1
PMCID: PMC168113  PMID: 8795207

Abstract

beta (1-->3)-Glucans are known for their potent ability to induce nonspecific inflammatory reactions and are believed to play a role in bioaerosol-induced respiratory symptoms. An inhibition enzyme immunoassay (EIA) was developed for the quantitation of beta (1-->3)-glucans in dust samples from occupational and residential environments. Immunospecific rabbit antibodies were produced by immunization with bovine serum albumin-conjugated laminarin [beta (1-->3)-glucan] and affinity chromatography on epoxy-Sepharose-coupled beta (1-->3)-glucans. The laminarin-based calibration curve in the inhibition EIA ranged from approximately 40 to 3,000 ng/ml (15 to 85% inhibition). Another beta (1-->3)-glucan (curdlan) showed a similar inhibition curve but was three to five times less reactive on a weight basis. Pustulan, presumed to be a beta (1-->6)-glucan, showed a parallel dose-response curve at concentrations 10 times higher than that of laminarin. Control experiments with NaIO4 and beta (1-->3)-glucanase treatment to destroy beta (1-->6)- and beta (1-->3)-glucan structures, respectively, indicate that the immunoreactivity of pustulan in the assay was due to beta (1-->3)-glucan and not to beta (1-->6)-glucan structures. Other polysaccharides, such as mannan and alpha (1-->6)-glucan, did not react in the inhibition EIA. Beta (1-->3)-Glucan extraction of dust samples in water (with mild detergent) was performed by heat treatment (120 degrees C) because aqueous extracts obtained at room temperature did not contain detectable beta (1-->3)-glucan levels. The assay was shown to detect heat-extractable beta (1-->3)-glucan in dust samples collected in a variety of occupational and environmental settings. On the basis of duplicate analyses of dust samples, a coefficient of variation of approximately 25% was calculated. It was concluded that the new inhibition EIA offers a useful method for indoor beta (1-->3)-glucan exposure assessment.

Full Text

The Full Text of this article is available as a PDF (308.8 KB).

Selected References

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

  1. Adachi Y., Ohno N., Yadomae T. Preparation and antigen specificity of an anti-(1-->3)-beta-D-glucan antibody. Biol Pharm Bull. 1994 Nov;17(11):1508–1512. doi: 10.1248/bpb.17.1508. [DOI] [PubMed] [Google Scholar]
  2. Adachi Y., Okazaki M., Ohno N., Yadomae T. Enhancement of cytokine production by macrophages stimulated with (1-->3)-beta-D-glucan, grifolan (GRN), isolated from Grifola frondosa. Biol Pharm Bull. 1994 Dec;17(12):1554–1560. doi: 10.1248/bpb.17.1554. [DOI] [PubMed] [Google Scholar]
  3. Aketagawa J., Tanaka S., Tamura H., Shibata Y., Saitô H. Activation of limulus coagulation factor G by several (1-->3)-beta-D-glucans: comparison of the potency of glucans with identical degree of polymerization but different conformations. J Biochem. 1993 Jun;113(6):683–686. doi: 10.1093/oxfordjournals.jbchem.a124103. [DOI] [PubMed] [Google Scholar]
  4. Brattgjerd S., Evensen O., Lauve A. Effect of injected yeast glucan on the activity of macrophages in Atlantic salmon, Salmo salar L., as evaluated by in vitro hydrogen peroxide production and phagocytic capacity. Immunology. 1994 Oct;83(2):288–294. [PMC free article] [PubMed] [Google Scholar]
  5. Clark C. S., Rylander R., Larsson L. Levels of gram-negative bacteria, Aspergillus fumigatus, dust, and endotoxin at compost plants. Appl Environ Microbiol. 1983 May;45(5):1501–1505. doi: 10.1128/aem.45.5.1501-1505.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. De Lucca A. J., 2nd, Brogden K. A., French A. D. Agglutination of lung surfactant with glucan. Br J Ind Med. 1992 Nov;49(11):755–760. doi: 10.1136/oem.49.11.755. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Di Luzio N. R. Lysozyme, glucan-activated macrophages and neoplasia. J Reticuloendothel Soc. 1979 Jul;26(1):67–81. [PubMed] [Google Scholar]
  8. Douwes J., Versloot P., Hollander A., Heederik D., Doekes G. Influence of various dust sampling and extraction methods on the measurement of airborne endotoxin. Appl Environ Microbiol. 1995 May;61(5):1763–1769. doi: 10.1128/aem.61.5.1763-1769.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Fogelmark B., Sjöstrand M., Rylander R. Pulmonary inflammation induced by repeated inhalations of beta(1,3)-D-glucan and endotoxin. Int J Exp Pathol. 1994 Apr;75(2):85–90. [PMC free article] [PubMed] [Google Scholar]
  10. Hirata A., Adachi Y., Itoh W., Komoda M., Tabata K., Sugawara I. Monoclonal antibody to proteoglycan derived from Grifola frondosa (Maitake). Biol Pharm Bull. 1994 Apr;17(4):539–542. doi: 10.1248/bpb.17.539. [DOI] [PubMed] [Google Scholar]
  11. Hirata A., Itoh W., Tabata K., Kojima T., Itoyama S., Sugawara I. Preparation and characterization of murine anti-schizophyllan monoclonal antibody, SPG1-HS. Biosci Biotechnol Biochem. 1993 Jan;57(1):125–126. doi: 10.1271/bbb.57.125. [DOI] [PubMed] [Google Scholar]
  12. Hirata A., Komoda M., Itoh W., Tabata K., Itoyama S., Sugawara I. An improved sandwich ELISA method for the determination of immunoreactive schizophyllan (SPG). Biol Pharm Bull. 1994 Nov;17(11):1437–1440. doi: 10.1248/bpb.17.1437. [DOI] [PubMed] [Google Scholar]
  13. Hutchins K., Bussey H. Cell wall receptor for yeast killer toxin: involvement of (1 leads to 6)-beta-D-glucan. J Bacteriol. 1983 Apr;154(1):161–169. doi: 10.1128/jb.154.1.161-169.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Mahauthaman R., Howell C. J., Spur B. W., Youlten L. J., Clark T. J., Lessof M. H., Lee T. H. The generation and cellular distribution of leukotriene C4 in human eosinophils stimulated by unopsonized zymosan and glucan particles. J Allergy Clin Immunol. 1988 Apr;81(4):696–705. doi: 10.1016/0091-6749(88)91041-x. [DOI] [PubMed] [Google Scholar]
  15. Mikami T., Nagase T., Matsumoto, Suzuki S., Suzuki M. Gelatin of Limulus amoebocyte lysate by simple polysaccharides. Microbiol Immunol. 1982;26(5):403–409. doi: 10.1111/j.1348-0421.1982.tb00190.x. [DOI] [PubMed] [Google Scholar]
  16. Montijn R. C., van Rinsum J., van Schagen F. A., Klis F. M. Glucomannoproteins in the cell wall of Saccharomyces cerevisiae contain a novel type of carbohydrate side chain. J Biol Chem. 1994 Jul 29;269(30):19338–19342. [PubMed] [Google Scholar]
  17. Nagi N., Ohno N., Adachi Y., Aketagawa J., Tamura H., Shibata Y., Tanaka S., Yadomae T. Application of limulus test (G pathway) for the detection of different conformers of (1-->3)-beta-D-glucans. Biol Pharm Bull. 1993 Sep;16(9):822–828. doi: 10.1248/bpb.16.822. [DOI] [PubMed] [Google Scholar]
  18. Obayashi T., Yoshida M., Mori T., Goto H., Yasuoka A., Iwasaki H., Teshima H., Kohno S., Horiuchi A., Ito A. Plasma (1-->3)-beta-D-glucan measurement in diagnosis of invasive deep mycosis and fungal febrile episodes. Lancet. 1995 Jan 7;345(8941):17–20. doi: 10.1016/s0140-6736(95)91152-9. [DOI] [PubMed] [Google Scholar]
  19. Preller L., Heederik D., Kromhout H., Boleij J. S., Tielen M. J. Determinants of dust and endotoxin exposure of pig farmers: development of a control strategy using empirical modelling. Ann Occup Hyg. 1995 Oct;39(5):545–557. [PubMed] [Google Scholar]
  20. Roslansky P. F., Novitsky T. J. Sensitivity of Limulus amebocyte lysate (LAL) to LAL-reactive glucans. J Clin Microbiol. 1991 Nov;29(11):2477–2483. doi: 10.1128/jcm.29.11.2477-2483.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Roy R., Katzenellenbogen E., Jennings H. J. Improved procedures for the conjugation of oligosaccharides to protein by reductive amination. Can J Biochem Cell Biol. 1984 May;62(5):270–275. doi: 10.1139/o84-037. [DOI] [PubMed] [Google Scholar]
  22. Sakurai T., Ohno N., Yadomae T. Changes in immune mediators in mouse lung produced by administration of soluble (1-->3)-beta-D-glucan. Biol Pharm Bull. 1994 May;17(5):617–622. doi: 10.1248/bpb.17.617. [DOI] [PubMed] [Google Scholar]
  23. Winston F., Dollard C., Ricupero-Hovasse S. L. Construction of a set of convenient Saccharomyces cerevisiae strains that are isogenic to S288C. Yeast. 1995 Jan;11(1):53–55. doi: 10.1002/yea.320110107. [DOI] [PubMed] [Google Scholar]
  24. Zhang K., Petty H. R. Influence of polysaccharides on neutrophil function: specific antagonists suggest a model for cooperative saccharide-associated inhibition of immune complex-triggered superoxide production. J Cell Biochem. 1994 Oct;56(2):225–235. doi: 10.1002/jcb.240560217. [DOI] [PubMed] [Google Scholar]

Articles from Applied and Environmental Microbiology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES