Molecular mimicry between Fc receptor and S peplomer protein of mouse hepatitis virus, bovine corona virus, and transmissible gastroenteritis virus
Identifieur interne : 000062 ( PascalFrancis/Checkpoint ); précédent : 000061; suivant : 000063Molecular mimicry between Fc receptor and S peplomer protein of mouse hepatitis virus, bovine corona virus, and transmissible gastroenteritis virus
Auteurs : E. L. Oleszak [États-Unis] ; J. Kuzmak [États-Unis] ; B. Hogue ; R. Parr ; E. W. Collisson ; L. S. Rodkey ; J. L. LeibowitzSource :
- Hybridoma [ 0272-457X ] ; 1995.
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- topic : Homme.
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Abstract
We have previously demonstrated molecular mimicry between the S peplomer protein of mouse hepatitis virus (MHV) and Fc gamma R (FcγR). A monoclonal antibody (MAb) to mouse FcγR (2.4G2 anti-FcγR MAb), purified rabbit immunoglobulin, but not their F(ab′)2 fragments, as well as mouse and rat IgG, immunoprecipitated (1) recombinant S peplomer protein expressed by a vaccinia virus recombinant in human, rabbit, and mouse cells, and (2) natural S peplomer protein from cells infected with several strains of MHV and MHV escape mutants. We report here results of studies documenting molecular mimicry between FcγR and S peplomer protein of viruses representing three distinct antigenic subgroups of the Coronaviridae. We have shown a molecular mimicry between the S peplomer protein of bovine corona virus (BCV) and FcγR. The 2.4G2 anti-FcγR MAb, rabbit IgG, but not its F(ab′)2 fragments, as well as homologous bovine serum, free of anti-BCV antibodies, immunoprecipitated S peplomer protein of BCV (Mebus strain). In contrast, we did not find molecular mimicry between S peplomer protein of human corona virus (HCV-OC43) and FcγR. Although the OC43 virus belongs to the same antigenic group as MHV and BCV, MAb specific for human FcγR I or FcγR II and purified human IgG1, IgG2, and IgG3 myeloma proteins did not immunoprecipitate the S peplomer protein from HCV-OC43-infected RD cells. In addition, we did demonstrate molecular mimicry between the S peplomer protein of porcine transmissible gastroenteritis virus (TGEV) and FcγR. TGEV belongs to the second antigenic subgroup of coronaviridae. Homologous swine IgG, but not its F(ab′)2 fragments, immunoprecipitated from TGEV-infected cells a 195-kDa polypeptide corresponding to the TGEV S peplomer protein. We have also examined whether there is a molecular mimicry between S peplomer protein of infectious bronchitis virus (IBV) and FcγR. Nonimmune chicken IgG did not immunoprecipitate the S peplomer protein from IBV-infected chicken embryo fibroblasts or Vero cells, suggesting that there is no molecular mimicry between the IBV-S and FcγR. In conclusion, we have demonstrated molecular mimicry between FcγR and S peplomer protein of three members of Coronaviridae, namely MHV, BCV, and TGEV. In contrast, the S peplomer protein of two other members of Coronaviridae, namely HCV-OC43 and IBV, did not exhibit any molecular mimicry with FcγR
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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Molecular mimicry between Fc receptor and S peplomer protein of mouse hepatitis virus, bovine corona virus, and transmissible gastroenteritis virus</title><author><name sortKey="Oleszak, E L" sort="Oleszak, E L" uniqKey="Oleszak E" first="E. L." last="Oleszak">E. L. Oleszak</name><affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Temple univ. school medicine, Fels inst. cancer res. molecular biology</s1><s2>Philadelphia PA 19140</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14><country>États-Unis</country><wicri:noRegion>Philadelphia PA 19140</wicri:noRegion></affiliation></author><author><name sortKey="Kuzmak, J" sort="Kuzmak, J" uniqKey="Kuzmak J" first="J." last="Kuzmak">J. Kuzmak</name><affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Temple univ. school medicine, Fels inst. cancer res. molecular biology</s1><s2>Philadelphia PA 19140</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14><country>États-Unis</country><wicri:noRegion>Philadelphia PA 19140</wicri:noRegion></affiliation></author><author><name sortKey="Hogue, B" sort="Hogue, B" uniqKey="Hogue B" first="B." last="Hogue">B. Hogue</name></author><author><name sortKey="Parr, R" sort="Parr, R" uniqKey="Parr R" first="R." last="Parr">R. Parr</name></author><author><name sortKey="Collisson, E W" sort="Collisson, E W" uniqKey="Collisson E" first="E. W." last="Collisson">E. W. Collisson</name></author><author><name sortKey="Rodkey, L S" sort="Rodkey, L S" uniqKey="Rodkey L" first="L. S." last="Rodkey">L. S. Rodkey</name></author><author><name sortKey="Leibowitz, J L" sort="Leibowitz, J L" uniqKey="Leibowitz J" first="J. L." last="Leibowitz">J. L. Leibowitz</name></author></titleStmt><publicationStmt><idno type="wicri:source">INIST</idno><idno type="inist">95-0193765</idno><date when="1995">1995</date><idno type="stanalyst">PASCAL 95-0193765 INIST</idno><idno type="RBID">Pascal:95-0193765</idno><idno type="wicri:Area/PascalFrancis/Corpus">000063</idno><idno type="wicri:Area/PascalFrancis/Curation">000067</idno><idno type="wicri:Area/PascalFrancis/Checkpoint">000062</idno><idno type="wicri:explorRef" wicri:stream="PascalFrancis" wicri:step="Checkpoint">000062</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Molecular mimicry between Fc receptor and S peplomer protein of mouse hepatitis virus, bovine corona virus, and transmissible gastroenteritis virus</title><author><name sortKey="Oleszak, E L" sort="Oleszak, E L" uniqKey="Oleszak E" first="E. L." last="Oleszak">E. L. Oleszak</name><affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Temple univ. school medicine, Fels inst. cancer res. molecular biology</s1><s2>Philadelphia PA 19140</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14><country>États-Unis</country><wicri:noRegion>Philadelphia PA 19140</wicri:noRegion></affiliation></author><author><name sortKey="Kuzmak, J" sort="Kuzmak, J" uniqKey="Kuzmak J" first="J." last="Kuzmak">J. Kuzmak</name><affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Temple univ. school medicine, Fels inst. cancer res. molecular biology</s1><s2>Philadelphia PA 19140</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14><country>États-Unis</country><wicri:noRegion>Philadelphia PA 19140</wicri:noRegion></affiliation></author><author><name sortKey="Hogue, B" sort="Hogue, B" uniqKey="Hogue B" first="B." last="Hogue">B. Hogue</name></author><author><name sortKey="Parr, R" sort="Parr, R" uniqKey="Parr R" first="R." last="Parr">R. Parr</name></author><author><name sortKey="Collisson, E W" sort="Collisson, E W" uniqKey="Collisson E" first="E. W." last="Collisson">E. W. Collisson</name></author><author><name sortKey="Rodkey, L S" sort="Rodkey, L S" uniqKey="Rodkey L" first="L. S." last="Rodkey">L. S. Rodkey</name></author><author><name sortKey="Leibowitz, J L" sort="Leibowitz, J L" uniqKey="Leibowitz J" first="J. L." last="Leibowitz">J. L. Leibowitz</name></author></analytic><series><title level="j" type="main">Hybridoma</title><title level="j" type="abbreviated">Hybridoma</title><idno type="ISSN">0272-457X</idno><imprint><date when="1995">1995</date></imprint></series></biblStruct></sourceDesc><seriesStmt><title level="j" type="main">Hybridoma</title><title level="j" type="abbreviated">Hybridoma</title><idno type="ISSN">0272-457X</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Biological receptor</term><term>Cross reaction</term><term>Human</term><term>IgG</term><term>Mimetism</term><term>Monoclonal antibody</term><term>Mouse</term><term>Murine hepatitis virus</term><term>Mutation</term><term>Porcine transmissible gastroenteritis virus</term><term>Recombinant protein</term><term>Serology</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Souris</term><term>Homme</term><term>Virus hépatite murine</term><term>Virus gastroentérite transmissible porc</term><term>Mutation</term><term>Mimétisme</term><term>Protéine recombinante</term><term>Anticorps monoclonal</term><term>Récepteur biologique</term><term>Sérologie</term><term>Réaction croisée</term><term>IgG</term><term>Récepteur Fcγ</term></keywords><keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Homme</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">We have previously demonstrated molecular mimicry between the S peplomer protein of mouse hepatitis virus (MHV) and Fc gamma R (FcγR). A monoclonal antibody (MAb) to mouse FcγR (2.4G2 anti-FcγR MAb), purified rabbit immunoglobulin, but not their F(ab′)<sub>2</sub> fragments, as well as mouse and rat IgG, immunoprecipitated (1) recombinant S peplomer protein expressed by a vaccinia virus recombinant in human, rabbit, and mouse cells, and (2) natural S peplomer protein from cells infected with several strains of MHV and MHV escape mutants. We report here results of studies documenting molecular mimicry between FcγR and S peplomer protein of viruses representing three distinct antigenic subgroups of the Coronaviridae. We have shown a molecular mimicry between the S peplomer protein of bovine corona virus (BCV) and FcγR. The 2.4G2 anti-FcγR MAb, rabbit IgG, but not its F(ab′)<sub>2</sub> fragments, as well as homologous bovine serum, free of anti-BCV antibodies, immunoprecipitated S peplomer protein of BCV (Mebus strain). In contrast, we did not find molecular mimicry between S peplomer protein of human corona virus (HCV-OC43) and FcγR. Although the OC43 virus belongs to the same antigenic group as MHV and BCV, MAb specific for human FcγR I or FcγR II and purified human IgG<sub>1</sub>, IgG<sub>2</sub>, and IgG<sub>3</sub> myeloma proteins did not immunoprecipitate the S peplomer protein from HCV-OC43-infected RD cells. In addition, we did demonstrate molecular mimicry between the S peplomer protein of porcine transmissible gastroenteritis virus (TGEV) and FcγR. TGEV belongs to the second antigenic subgroup of coronaviridae. Homologous swine IgG, but not its F(ab′)<sub>2</sub> fragments, immunoprecipitated from TGEV-infected cells a 195-kDa polypeptide corresponding to the TGEV S peplomer protein. We have also examined whether there is a molecular mimicry between S peplomer protein of infectious bronchitis virus (IBV) and FcγR. Nonimmune chicken IgG did not immunoprecipitate the S peplomer protein from IBV-infected chicken embryo fibroblasts or Vero cells, suggesting that there is no molecular mimicry between the IBV-S and FcγR. In conclusion, we have demonstrated molecular mimicry between FcγR and S peplomer protein of three members of Coronaviridae, namely MHV, BCV, and TGEV. In contrast, the S peplomer protein of two other members of Coronaviridae, namely HCV-OC43 and IBV, did not exhibit any molecular mimicry with FcγR</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0272-457X</s0></fA01><fA02 i1="01"><s0>HYBRDY</s0></fA02><fA03 i2="1"><s0>Hybridoma</s0></fA03><fA05><s2>14</s2></fA05><fA06><s2>1</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Molecular mimicry between Fc receptor and S peplomer protein of mouse hepatitis virus, bovine corona virus, and transmissible gastroenteritis virus</s1></fA08><fA11 i1="01" i2="1"><s1>OLESZAK (E. L.)</s1></fA11><fA11 i1="02" i2="1"><s1>KUZMAK (J.)</s1></fA11><fA11 i1="03" i2="1"><s1>HOGUE (B.)</s1></fA11><fA11 i1="04" i2="1"><s1>PARR (R.)</s1></fA11><fA11 i1="05" i2="1"><s1>COLLISSON (E. W.)</s1></fA11><fA11 i1="06" i2="1"><s1>RODKEY (L. S.)</s1></fA11><fA11 i1="07" i2="1"><s1>LEIBOWITZ (J. L.)</s1></fA11><fA14 i1="01"><s1>Temple univ. school medicine, Fels inst. cancer res. molecular biology</s1><s2>Philadelphia PA 19140</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></fA14><fA20><s1>1-8</s1></fA20><fA21><s1>1995</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>20384</s2><s5>354000055692160010</s5></fA43><fA44><s0>0000</s0></fA44><fA45><s0>74 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>95-0193765</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Hybridoma</s0></fA64><fA66 i1="01"><s0>USA</s0></fA66><fC01 i1="01" l="ENG"><s0>We have previously demonstrated molecular mimicry between the S peplomer protein of mouse hepatitis virus (MHV) and Fc gamma R (FcγR). A monoclonal antibody (MAb) to mouse FcγR (2.4G2 anti-FcγR MAb), purified rabbit immunoglobulin, but not their F(ab′)<sub>2</sub> fragments, as well as mouse and rat IgG, immunoprecipitated (1) recombinant S peplomer protein expressed by a vaccinia virus recombinant in human, rabbit, and mouse cells, and (2) natural S peplomer protein from cells infected with several strains of MHV and MHV escape mutants. We report here results of studies documenting molecular mimicry between FcγR and S peplomer protein of viruses representing three distinct antigenic subgroups of the Coronaviridae. We have shown a molecular mimicry between the S peplomer protein of bovine corona virus (BCV) and FcγR. The 2.4G2 anti-FcγR MAb, rabbit IgG, but not its F(ab′)<sub>2</sub> fragments, as well as homologous bovine serum, free of anti-BCV antibodies, immunoprecipitated S peplomer protein of BCV (Mebus strain). In contrast, we did not find molecular mimicry between S peplomer protein of human corona virus (HCV-OC43) and FcγR. Although the OC43 virus belongs to the same antigenic group as MHV and BCV, MAb specific for human FcγR I or FcγR II and purified human IgG<sub>1</sub>, IgG<sub>2</sub>, and IgG<sub>3</sub> myeloma proteins did not immunoprecipitate the S peplomer protein from HCV-OC43-infected RD cells. In addition, we did demonstrate molecular mimicry between the S peplomer protein of porcine transmissible gastroenteritis virus (TGEV) and FcγR. TGEV belongs to the second antigenic subgroup of coronaviridae. Homologous swine IgG, but not its F(ab′)<sub>2</sub> fragments, immunoprecipitated from TGEV-infected cells a 195-kDa polypeptide corresponding to the TGEV S peplomer protein. We have also examined whether there is a molecular mimicry between S peplomer protein of infectious bronchitis virus (IBV) and FcγR. Nonimmune chicken IgG did not immunoprecipitate the S peplomer protein from IBV-infected chicken embryo fibroblasts or Vero cells, suggesting that there is no molecular mimicry between the IBV-S and FcγR. In conclusion, we have demonstrated molecular mimicry between FcγR and S peplomer protein of three members of Coronaviridae, namely MHV, BCV, and TGEV. 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W." last="Collisson">E. W. Collisson</name><name sortKey="Hogue, B" sort="Hogue, B" uniqKey="Hogue B" first="B." last="Hogue">B. Hogue</name><name sortKey="Leibowitz, J L" sort="Leibowitz, J L" uniqKey="Leibowitz J" first="J. L." last="Leibowitz">J. L. Leibowitz</name><name sortKey="Parr, R" sort="Parr, R" uniqKey="Parr R" first="R." last="Parr">R. Parr</name><name sortKey="Rodkey, L S" sort="Rodkey, L S" uniqKey="Rodkey L" first="L. S." last="Rodkey">L. S. Rodkey</name></noCountry><country name="États-Unis"><noRegion><name sortKey="Oleszak, E L" sort="Oleszak, E L" uniqKey="Oleszak E" first="E. L." last="Oleszak">E. L. Oleszak</name></noRegion><name sortKey="Kuzmak, J" sort="Kuzmak, J" uniqKey="Kuzmak J" first="J." last="Kuzmak">J. Kuzmak</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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