Glycosylation is Required for Coronavirus TGEV to Induce an Efficient Production of IFNα by Blood Mononuclear Cells

Porcine peripheral blood mononuclear cells (PBMC) are induced to produce interferon alpha (IFNα) following in vitro exposure to coronavirus TGEV (transmissible gastroenteritis virus)‐infected glutaraldehyde‐fixed cell monolayers or lo TGEV virions. In the present report, we examined the possibility that glycosylation of viral proteins could play a major role in interactions with PBMC leading to the production of IFNα. Con A pretreatment of TGEV‐infected cell monolayers before fixation with glutaraldehyde and exposure to PBMC caused a dose‐dependent inhibition of IFNα induction, implying that masking of carbohydrates at the surface of infected cells lowered IFNα induction. Similarly, inhibition of N‐linked glycosylation by tunicamycin during viral infection of cell monolayers altered their ability to induce IFNα. In addition, complete cleavage of complex type' oligosaccharides by peptide‐N‐glycohydrolase Flowered the capacity of TGEV virions to induce IFNα. Thus, these findings strongly suggest that glycosylation of the viral proteins, and more precisely the presence of complex‐type oligosaccharides, is an important requirement for a completely efficient interaction with PBMC leading to the production of IFN‐α.

[1]  B. Delmas,et al.  Assembly of coronavirus spike protein into trimers and its role in epitope expression , 1990, Journal of virology.

[2]  Timothy A. Springer,et al.  Adhesion receptors of the immune system , 1990, Nature.

[3]  P. Matsson,et al.  A distinct population of nonphagocytic and low level CD4+ null lymphocytes produce IFN-alpha after stimulation by herpes simplex virus-infected cells. , 1990, Journal of immunology.

[4]  L. Lavenant,et al.  Characterization of blood mononuclear cells producing IFNα following induction by coronavirus-infected cells (porcine transmissible gastroenteritis virus) , 1990, Research in Immunology.

[5]  G. Alm,et al.  Infrequent but efficient interferon-alpha-producing human mononuclear leukocytes induced by herpes simplex virus in vitro studied by immuno-plaque and limiting dilution assays. , 1990, Journal of interferon research.

[6]  R. B. Trimble,et al.  Enzymatic approaches for studying the structure, synthesis, and processing of glycoproteins. , 1989, Methods in cell biology.

[7]  K. Funa,et al.  Different induction patterns of mRNA for IFN-alpha and -beta in human mononuclear leukocytes after in vitro stimulation with herpes simplex virus-infected fibroblasts and Sendai virus. , 1988, Journal of immunology.

[8]  P. Fitzgerald-Bocarsly,et al.  Human Mononuclear Cells Which Produce Interferon‐Alpha During NK(HSV‐FS) Assays Are HLA‐DR Positive Cells Distinct From Cytolytic Natural Killer Effectors , 1988, Journal of leukocyte biology.

[9]  G. Alm,et al.  Determination of Herpes Simplex Virus‐Induced Alpha Interferon‐Secreting Human Blood Leucocytes by a Filter Immuno‐Plaque Assay , 1988, Scandinavian journal of immunology.

[10]  H. Laude,et al.  Induction of alpha interferon by transmissible gastroenteritis coronavirus: role of transmembrane glycoprotein E1 , 1988, Journal of virology.

[11]  D. Miller,et al.  Cooperation between CD16(Leu-11b)+ NK cells and HLA-DR+ cells in natural killing of herpesvirus-infected fibroblasts. , 1987, Journal of immunology.

[12]  H. Laude,et al.  Sequence and N-terminal processing of the transmembrane protein E1 of the coronavirus transmissible gastroenteritis virus. , 1987, The Journal of general virology.

[13]  A. Elbein,et al.  Inhibitors of the biosynthesis and processing of N-linked oligosaccharide chains. , 1987, Annual review of biochemistry.

[14]  F. Ennis,et al.  Induction of interferon alpha and gamma from human lymphocytes by dengue virus-infected cells. , 1986, The Journal of general virology.

[15]  J. Grosclaude,et al.  Antigenic structure of transmissible gastroenteritis virus. I. Properties of monoclonal antibodies directed against virion proteins. , 1986, The Journal of general virology.

[16]  P. Lebon Inhibition of herpes simplex virus type 1-induced interferon synthesis by monoclonal antibodies against viral glycoprotein D and by lysosomotropic drugs. , 1985, The Journal of general virology.

[17]  C. Machamer,et al.  A single N-linked oligosaccharide at either of the two normal sites is sufficient for transport of vesicular stomatitis virus G protein to the cell surface , 1985, Molecular and cellular biology.

[18]  G. Antonelli,et al.  Induction of Alpha Interferon by Membrane Interaction between Viral Surface and Peripheral Blood Mononuclear Cells , 1985, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

[19]  Y. Shirako,et al.  Two Purified RNAs of Soil-borne Wheat Mosaic Virus are Needed for Infection , 1984 .

[20]  P. Lebon,et al.  Different mechanisms for a and interferon induction , 1982 .

[21]  H. Laude,et al.  High interferon titer in newborn pig intestine during experimentally induced viral enteritis , 1981, Infection and immunity.

[22]  R. Zawatzky,et al.  Human peripheral null lymphocytes II. Producers of type‐1 interferon upon stimulation with tumor cells, Herpes simplex virus and Corynebacterium parvum , 1980, European journal of immunology.

[23]  J U Baenziger,et al.  Structural determinants of concanavalin A specificity for oligosaccharides. , 1979, The Journal of biological chemistry.

[24]  Y. Ito,et al.  The mechanism of interferon induction in mouse spleen cells stimulated with HVJ. , 1978, Virology.