Skip to main content
Log in

Molecular differentiation in pea powdery-mildew haustoria

Identification of a 62-kDa N-linked glycoprotein unique to the haustorial plasma membrane

  • Published:
Planta Aims and scope Submit manuscript

Abstract

Monoclonal antibodies have been raised against haustorial complexes isolated from pea (Pisum sativum L.) leaves infected by the biotrophic powdery mildew fungus Erysiphe pisi D.C. Immuno-localisation studies, using isolated haustorial complexes and infected pea leaf material, have shown that one of the antibodies, designated UB7, binds to fungal wall and plasma membranes present in both haustoria and mycelia. However, a second antibody, UB8, binds specifically to the haustorial plasma membrane, and does not label fungal plasma membranes in mycelia. Western blotting and antigen-modification techniques have shown that UB8 recognises a protein epitope of a 62-kDa antigen. A reduction in molecular weight of this component after endo-F treatment indicates that the antigen is an N-linked glycoprotein. UB7 also recognises a 62-kDa glycoprotein, which is susceptible to endo-F treatment, and the antibody binds to a carbohydrate epitope. Differences in molecular weights of the products after endo-F treatment of antigens show that the 62-kDa glycoproteins recognised by the antibodies are distinct molecules, in accordance with the localisation results. Overall, the results provide evidence for molecular differentiation associated with the development of haustoria in a biotrophic infection.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

ehm :

extrahaustorial membrane

ELISA:

enzyme-linked immunosorbent assay

HC:

haustorial complex

hpm :

haustorial plasma membrane

IIF:

indirect immunofluorescence

MAb:

monoclonal antibody

Mr :

apparent molecular weight

PMSF:

phenylmethylsulfonyl fluoride

SDS-PAGE:

sodium dodecyl sulphate-polyacrylamide gel electrophoresis

References

  • Bartnicki-Garcia, S. (1968) Cell wall chemistry, morphogenesis and taxonomy. Ann. Rev. Microbiol. 22, 87–108

    Google Scholar 

  • Behnke, O., Ammitzboll, T., Jessen, H., Klokker, M., Nilausen, K., Tranum-Jensen, J., Olsson, L. (1986) Non-specific binding of protein stabilised gold sols as a source of error in immunocytochemistry. Eur. J. Cell Biol. 41, 326–338

    Google Scholar 

  • Birk, H., Koepsell, H. (1987) Reaction of monoclonal antibodies with plasma membrane proteins after binding on nitrocellulose: renaturation of antigenic sites and reduction of nonspecific antibody binding. Anal. Biochem. 164, 12–22

    Google Scholar 

  • Bushnell, W.R., Gay, J.L. (1978) Accumulation of solutes in relation to the structure and function of haustoria in powdery mildews. In: The powdery mildews, pp. 183–235, Spencer, D.M., ed. Academic Press, London

    Google Scholar 

  • Chard, J.M., Gay, J.L. (1984) Characterisation of the parasitic interface between Erysiphe pisi and Pisum sativum using fluorescent probes. Physiol. Plant Pathol. 25, 259–276

    Google Scholar 

  • Chong, J., Harder, D.E., Rohringer, R. (1986) Cytochemical studies on Puccinia graminis f. sp. tritici in a compatible wheat host. II. Haustorium mother cell walls at the host penetration site, haustorial walls, and the extrahaustorial matrix. Can. J. Bot. 64, 2561–2575

    Google Scholar 

  • Estrada-Garcia, M.T., Green, J.R., Booth, J.M., White, J.G., Callow, J.A. (1989) Monoclonal antibodies to cell surface components of zoospores and cysts of the fungus Pythium aphanidermatum reveal species-specific antigens. Exp. Mycol. 13, 348–355

    Google Scholar 

  • Galfre, G., Milstein, C. (1981) Preparation of monoclonal antibodies: strategies and procedures. Methods Enzymol. 73, 1–46

    Google Scholar 

  • Gay, J.L., Manners, J.M. (1987) Permeability of the haustorium-host interface in powdery mildews. Physiol. Mol. Plant Pathol. 30, 389–399

    Google Scholar 

  • Gay, J.L., Salzberg, A., Woods, A.M. (1987) Dynamic experimental evidence for the plasma membrane ATPase domain hypothesis of haustorial transport and for ionic coupling of the haustorium of Erysiphe graminis to the host cell (Hordeum vulgare). New Phytol. 107, 541–548

    Google Scholar 

  • Gil, F., Gay, J.L. (1977) Ultrastructural and physiological properties of the host interfacial components of haustoria of Erysiphe pisi in vitro and in vivo. Physiol. Plant Pathol. 10, 1–12

    Google Scholar 

  • Gloudemans, T., de Vries, S., Bussink, H.J., Malik, N.S.A., Fransssen, H.J., Louwerse, J., Bisseling, T. (1987) Nodulin gene expression during soybean (Glycine max) nodule development. Plant Mol. Biol. 8, 395–403

    Google Scholar 

  • Hahn, M.G., Lerner, D.R., Fitter, M.S., Norman, P.M., Lamb, C.J. (1987) Characterisation of monoclonal antibodies to protoplast membranes of Nicotiana tabacum identified by an enzyme-linked immunosorbent assay. Planta 171, 453–465

    Google Scholar 

  • Jones, J.L., Callow, J.A., Green, J.R. (1988) Monoclonal antibodies to sperm surface antigens of the brown alga Fucus serratus exhibit region-, gamete-, species- and genus-preferential binding. Planta 176, 298–306

    Google Scholar 

  • Key, G., Weiler, E.W. (1988) Monoclonal antibodies identify common and differentiation specific antigens on the plasma membrane of guard cells of Vicia faba L. Planta 176, 472–481

    Google Scholar 

  • Knox, J.P., Day, S., Roberts, K. (1989) A set of cell surface glycoproteins forms an early marker of cell position, but not cell type, in the root apical meristem of Daucus carota L. Development 106, 47–56

    Google Scholar 

  • Laemmli, U.K. (1970) Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227, 680–685

    PubMed  Google Scholar 

  • Lancelle, S.A., Hepler, P.K. (1989) Immunogold labelling of actin on sections of freeze-substituted plant cells. Protoplasma 150, 72–74

    Google Scholar 

  • Manners, J.M. (1989) The host-haustorium interface in powdery mildews. Aust. J. Plant Physiol. 16, 45–52

    Google Scholar 

  • Manners, J.M., Gay, J.L. (1982) Transport, translocation and metabolism of 14C-photosynthates at the host-parasite interface of Pisum sativum and Erysiphe pisi. New Phytol. 91, 221–244

    Google Scholar 

  • Manners, J.M., Gay, J.L. (1983) The host-parasite interface and nutrient transfer in biotrophic parasitism. In: Biochemical plant pathology, pp. 163–195, Callow, J.A., ed. Wiley, Chichester

    Google Scholar 

  • Mendgen, K., Schneider, A., Sterk, M., Fink, W. (1988) The differentiation of infection structures as a result of recognition events between some biotrophic parasites and their hosts. J. Phytopathol. 123, 259–272

    Google Scholar 

  • Smith, S.E., Smith, F.A. (1990) Structure and function of the interfaces in biotrophic symbioses as they relate to nutrient transport. New Phytol. 114, 1–38

    Google Scholar 

  • Spencer-Phillips, P.T.N., Gay, J.L. (1981) Domains of ATPase in plasma membranes and transport through infected plant cells. New Phytol. 89, 393–400

    Google Scholar 

  • Sussman, M.R., Surowy, T.K. (1987) Physiology and molecular biology of membrane ATPases. In: Oxford Surveys of Plant Molecular and Cell Biology, vol. 4, pp. 47–71. Miflin, B.J., ed.

  • Tarentino, A.L., Gomez, C.M., Plummer, T.H. (1985) De-glycosylation of asparagine-linked glycans by peptide: N-glycosidase F. Biochemistry 24, 4665–4671

    Google Scholar 

  • Umemoto, J., Bhavanandan, V.P., Davidson, E.A. (1977) Purification and properties of an endo-N-acetly-d-galactosaminidase from Diplococcus pneumoniae. J. Biol. Chem. 252, 8609–8614

    Google Scholar 

  • Verma, D.P.S., Fortin, M.G., Stanley, J., Mauro, V.P., Purohit, S., Morrison, N. (1986) Nodulins and nodulin genes of Glycine max. Plant Mol. Biol. 7, 51–61

    Google Scholar 

  • Williams, A.F., Barclay, A.N. (1986) Glycoprotein antigens of the lymphocyte surface and their purification by antibody affinity chromatography. In: Handbook of experimental immunology, 4th edn., chpt. 22, Weir, D.M., ed. Blackwell, Oxford

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

We thank Mr. D. Mills and Mr. P. Stanley for help with the EM immunogold techniques. This work was supported by an Agricultural and Food Research Council grant and a studentship from the Science and Engineering Research Council.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Mackie, A.J., Roberts, A.M., Callow, J.A. et al. Molecular differentiation in pea powdery-mildew haustoria. Planta 183, 399–408 (1991). https://doi.org/10.1007/BF00197739

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00197739

Key words

Navigation