The immunoprotective Anaplasma marginale major surface protein 2 is encoded by a polymorphic multigene family

An Anaplasma marginale Florida msp-2 gene was cloned and expressed in Escherichia coli. Pulsed-field gel electrophoresis and Southern blot analysis revealed the presence of multiple msp-2 gene copies that were widely distributed throughout the chromosomes of all three strains examined. Genomic polym...

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Veröffentlicht in:Infection and Immunity 1994-09, Vol.62 (9), p.3808-3816
Hauptverfasser: Palmer, G.H. (Washington State University, Pullman, WA.), Eid, G, Barbet, A.F, McGuire, T.C, McElwain, T.F
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container_end_page 3816
container_issue 9
container_start_page 3808
container_title Infection and Immunity
container_volume 62
creator Palmer, G.H. (Washington State University, Pullman, WA.)
Eid, G
Barbet, A.F
McGuire, T.C
McElwain, T.F
description An Anaplasma marginale Florida msp-2 gene was cloned and expressed in Escherichia coli. Pulsed-field gel electrophoresis and Southern blot analysis revealed the presence of multiple msp-2 gene copies that were widely distributed throughout the chromosomes of all three strains examined. Genomic polymorphism among copies was greatest in the 5' end of msp-2 but also occurred in 3' regions. The presence of gene-copy-specific epitopes was indicated by the reactivity of the cloned msp-2 copy with some, but not all, monoclonal antibodies that bound native MSP-2. Multiple antigenically distinct MSP-2 molecules were expressed within strains and were coexpressed by individual A. marginale organisms. These results suggest that expression of polymorphic msp-2 gene copies is responsible for the significant percentages of A. marginale organisms within strains that do not react with individual anti-MSP-2 monoclonal antibodies. Sequence analysis revealed highly significant MSP-2 homology with two rickettsial surface proteins, A. marginale MSP-4 and Cowdria ruminantium MAP-1. Immunization with MSP-4 has been shown to induce protective immunity in a manner similar to that of immunization with MSP-2. These findings support the hypothesis that A. marginale surface proteins are targets of protective immune responses but are antigenically polymorphic
doi_str_mv 10.1128/IAI.62.9.3808-3816.1994
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(Washington State University, Pullman, WA.) ; Eid, G ; Barbet, A.F ; McGuire, T.C ; McElwain, T.F</creator><creatorcontrib>Palmer, G.H. (Washington State University, Pullman, WA.) ; Eid, G ; Barbet, A.F ; McGuire, T.C ; McElwain, T.F</creatorcontrib><description>An Anaplasma marginale Florida msp-2 gene was cloned and expressed in Escherichia coli. Pulsed-field gel electrophoresis and Southern blot analysis revealed the presence of multiple msp-2 gene copies that were widely distributed throughout the chromosomes of all three strains examined. Genomic polymorphism among copies was greatest in the 5' end of msp-2 but also occurred in 3' regions. The presence of gene-copy-specific epitopes was indicated by the reactivity of the cloned msp-2 copy with some, but not all, monoclonal antibodies that bound native MSP-2. Multiple antigenically distinct MSP-2 molecules were expressed within strains and were coexpressed by individual A. marginale organisms. These results suggest that expression of polymorphic msp-2 gene copies is responsible for the significant percentages of A. marginale organisms within strains that do not react with individual anti-MSP-2 monoclonal antibodies. Sequence analysis revealed highly significant MSP-2 homology with two rickettsial surface proteins, A. marginale MSP-4 and Cowdria ruminantium MAP-1. Immunization with MSP-4 has been shown to induce protective immunity in a manner similar to that of immunization with MSP-2. 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(Washington State University, Pullman, WA.)</creatorcontrib><creatorcontrib>Eid, G</creatorcontrib><creatorcontrib>Barbet, A.F</creatorcontrib><creatorcontrib>McGuire, T.C</creatorcontrib><creatorcontrib>McElwain, T.F</creatorcontrib><title>The immunoprotective Anaplasma marginale major surface protein 2 is encoded by a polymorphic multigene family</title><title>Infection and Immunity</title><addtitle>Infect Immun</addtitle><description>An Anaplasma marginale Florida msp-2 gene was cloned and expressed in Escherichia coli. Pulsed-field gel electrophoresis and Southern blot analysis revealed the presence of multiple msp-2 gene copies that were widely distributed throughout the chromosomes of all three strains examined. Genomic polymorphism among copies was greatest in the 5' end of msp-2 but also occurred in 3' regions. The presence of gene-copy-specific epitopes was indicated by the reactivity of the cloned msp-2 copy with some, but not all, monoclonal antibodies that bound native MSP-2. Multiple antigenically distinct MSP-2 molecules were expressed within strains and were coexpressed by individual A. marginale organisms. These results suggest that expression of polymorphic msp-2 gene copies is responsible for the significant percentages of A. marginale organisms within strains that do not react with individual anti-MSP-2 monoclonal antibodies. Sequence analysis revealed highly significant MSP-2 homology with two rickettsial surface proteins, A. marginale MSP-4 and Cowdria ruminantium MAP-1. Immunization with MSP-4 has been shown to induce protective immunity in a manner similar to that of immunization with MSP-2. These findings support the hypothesis that A. marginale surface proteins are targets of protective immune responses but are antigenically polymorphic</description><subject>Amino Acid Sequence</subject><subject>ANAPLASMA</subject><subject>Anaplasma - genetics</subject><subject>Anaplasma - immunology</subject><subject>Anaplasma marginale</subject><subject>Antibodies, Monoclonal - immunology</subject><subject>ANTIGENE</subject><subject>ANTIGENOS</subject><subject>Bacterial Proteins - chemistry</subject><subject>Bacterial Proteins - genetics</subject><subject>Bacterial Proteins - immunology</subject><subject>Bacteriology</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>CLONACION</subject><subject>CLONAGE</subject><subject>Cloning, Molecular</subject><subject>DIFERENCIAS BIOLOGICAS</subject><subject>DIFFERENCE BIOLOGIQUE</subject><subject>ESCHERICHIA COLI</subject><subject>EXPRESION GENICA</subject><subject>EXPRESSION DES GENES</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>GENE</subject><subject>GENES</subject><subject>Genes, Bacterial</subject><subject>Genetics</subject><subject>GLICOPROTEINAS</subject><subject>GLYCOPROTEINE</subject><subject>Microbiology</subject><subject>Molecular Sequence Data</subject><subject>Multigene Family</subject><subject>POLIMORFISMO GENETICO</subject><subject>POLYMORPHISME GENETIQUE</subject><subject>SECUENCIA NUCLEICA</subject><subject>SEQUENCE NUCLEIQUE</subject><issn>0019-9567</issn><issn>1098-5522</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUurEzEYhoMox1r9A4IYQdxNnVxnsnBRDl4KB1xY1-FrLm0OM5MxmTnSf29qS_GsJIskfM_73V6E3pJ6RQhtP27Wm5WkK7Vibd1WrCVyRZTiT9CC1KqthKD0KVrUNVGVErJ5jl7kfF--nPP2Bt20tWRMNQvUbw8Oh76fhzimODkzhQeH1wOMHeQecA9pHwboXHndx4TznDwYh__CYcAUh4zdYKJ1Fu-OGPAYu2Mf03gIBvdzN4W9Gxz20Ifu-BI989Bl9-pyL9H2y-ft7bfq7vvXze36rjKCyKmy3lhhVcOsFTsQTFIqvffOgxfKGLZjwjeO74DZVjFuSVMWALZtjOGccrZEn85px3nXO2vcMCXo9JhCGeeoIwT9ODKEg97HB83qckTRf7joU_w1uzzpPmTjug4GF-esGyklJ_L_IJGqKdunBWzOoEkx5-T8tRlS65OhOpSmJNVKnwzVJ0P1ydCifPPvLFfdxcESf3-JQzbQ-QSDCfmKcSqJKOQSvTtjh7A__A7J6WLv46KFeX1mPEQN-1TS_PyhBGdtw9kfBy_A5g</recordid><startdate>19940901</startdate><enddate>19940901</enddate><creator>Palmer, G.H. 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(Washington State University, Pullman, WA.) ; Eid, G ; Barbet, A.F ; McGuire, T.C ; McElwain, T.F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c516t-dfcd5d973dd5ba536226fffefaf59cc3b35f7e4ba3d8934d17381ad87cc44243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Amino Acid Sequence</topic><topic>ANAPLASMA</topic><topic>Anaplasma - genetics</topic><topic>Anaplasma - immunology</topic><topic>Anaplasma marginale</topic><topic>Antibodies, Monoclonal - immunology</topic><topic>ANTIGENE</topic><topic>ANTIGENOS</topic><topic>Bacterial Proteins - chemistry</topic><topic>Bacterial Proteins - genetics</topic><topic>Bacterial Proteins - immunology</topic><topic>Bacteriology</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>CLONACION</topic><topic>CLONAGE</topic><topic>Cloning, Molecular</topic><topic>DIFERENCIAS BIOLOGICAS</topic><topic>DIFFERENCE BIOLOGIQUE</topic><topic>ESCHERICHIA COLI</topic><topic>EXPRESION GENICA</topic><topic>EXPRESSION DES GENES</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>GENE</topic><topic>GENES</topic><topic>Genes, Bacterial</topic><topic>Genetics</topic><topic>GLICOPROTEINAS</topic><topic>GLYCOPROTEINE</topic><topic>Microbiology</topic><topic>Molecular Sequence Data</topic><topic>Multigene Family</topic><topic>POLIMORFISMO GENETICO</topic><topic>POLYMORPHISME GENETIQUE</topic><topic>SECUENCIA NUCLEICA</topic><topic>SEQUENCE NUCLEIQUE</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Palmer, G.H. (Washington State University, Pullman, WA.)</creatorcontrib><creatorcontrib>Eid, G</creatorcontrib><creatorcontrib>Barbet, A.F</creatorcontrib><creatorcontrib>McGuire, T.C</creatorcontrib><creatorcontrib>McElwain, T.F</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Infection and Immunity</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Palmer, G.H. (Washington State University, Pullman, WA.)</au><au>Eid, G</au><au>Barbet, A.F</au><au>McGuire, T.C</au><au>McElwain, T.F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The immunoprotective Anaplasma marginale major surface protein 2 is encoded by a polymorphic multigene family</atitle><jtitle>Infection and Immunity</jtitle><addtitle>Infect Immun</addtitle><date>1994-09-01</date><risdate>1994</risdate><volume>62</volume><issue>9</issue><spage>3808</spage><epage>3816</epage><pages>3808-3816</pages><issn>0019-9567</issn><eissn>1098-5522</eissn><coden>INFIBR</coden><abstract>An Anaplasma marginale Florida msp-2 gene was cloned and expressed in Escherichia coli. Pulsed-field gel electrophoresis and Southern blot analysis revealed the presence of multiple msp-2 gene copies that were widely distributed throughout the chromosomes of all three strains examined. Genomic polymorphism among copies was greatest in the 5' end of msp-2 but also occurred in 3' regions. The presence of gene-copy-specific epitopes was indicated by the reactivity of the cloned msp-2 copy with some, but not all, monoclonal antibodies that bound native MSP-2. Multiple antigenically distinct MSP-2 molecules were expressed within strains and were coexpressed by individual A. marginale organisms. These results suggest that expression of polymorphic msp-2 gene copies is responsible for the significant percentages of A. marginale organisms within strains that do not react with individual anti-MSP-2 monoclonal antibodies. Sequence analysis revealed highly significant MSP-2 homology with two rickettsial surface proteins, A. marginale MSP-4 and Cowdria ruminantium MAP-1. Immunization with MSP-4 has been shown to induce protective immunity in a manner similar to that of immunization with MSP-2. These findings support the hypothesis that A. marginale surface proteins are targets of protective immune responses but are antigenically polymorphic</abstract><cop>Washington, DC</cop><pub>American Society for Microbiology</pub><pmid>8063397</pmid><doi>10.1128/IAI.62.9.3808-3816.1994</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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source American Society for Microbiology; MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central
subjects Amino Acid Sequence
ANAPLASMA
Anaplasma - genetics
Anaplasma - immunology
Anaplasma marginale
Antibodies, Monoclonal - immunology
ANTIGENE
ANTIGENOS
Bacterial Proteins - chemistry
Bacterial Proteins - genetics
Bacterial Proteins - immunology
Bacteriology
Base Sequence
Biological and medical sciences
CLONACION
CLONAGE
Cloning, Molecular
DIFERENCIAS BIOLOGICAS
DIFFERENCE BIOLOGIQUE
ESCHERICHIA COLI
EXPRESION GENICA
EXPRESSION DES GENES
Fundamental and applied biological sciences. Psychology
GENE
GENES
Genes, Bacterial
Genetics
GLICOPROTEINAS
GLYCOPROTEINE
Microbiology
Molecular Sequence Data
Multigene Family
POLIMORFISMO GENETICO
POLYMORPHISME GENETIQUE
SECUENCIA NUCLEICA
SEQUENCE NUCLEIQUE
title The immunoprotective Anaplasma marginale major surface protein 2 is encoded by a polymorphic multigene family
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