Characterization of recombinant foot-and-mouth disease virus pentamer-like structures expressed by baculovirus and their use as diagnostic antigens in a blocking ELISA
Abstract Non-infectious recombinant pentamer-like structures of the foot-and-mouth disease virus (FMDV) were expressed by baculovirus, and the antigenicity and immunogenicity of the proteins were analyzed in a blocking ELISA for the detection of FMDV antibodies. The recombinant pentamer-like structu...
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description | Abstract Non-infectious recombinant pentamer-like structures of the foot-and-mouth disease virus (FMDV) were expressed by baculovirus, and the antigenicity and immunogenicity of the proteins were analyzed in a blocking ELISA for the detection of FMDV antibodies. The recombinant pentamer-like structures were produced in insect (Sf9) cells that were inoculated with recombinant baculoviruses that expressed, simultaneously, the genes for the P1 and 3C proteins of FMDV from individual promoters. The FMDV pentamer-like structures were processed by viral 3C protease, as shown in Western blots, and were antigenic, as revealed by their reactivities in an indirect ELISA. Analysis by CsCl gradient centrifugation showed that the pentamer-like structures were similar to authentic pentameric subunits from FMDV in terms of sedimentation velocity. Furthermore, the pentamer-like structures induced high levels of FMDV-specific antibodies in mice following immunization. Observations made under the electron microscope revealed that the pentamer-like structures expressed by insect cells self-assembled to form pentameric subunits of 7–8 nm in diameter, which resemble the authentic FMDV (23 ± 2 nm in diameter). The results indicate that these pentamer-like structures are as antigenic and immunogenic as authentic FMDV, although the former are smaller in size. Based on these results, a blocking ELISA was developed using the recombinant pentamer-like structure. The ELISA showed specificity of 99.5% and sensitivity of 98.5% when tested with FMDV antibody-negative and -positive sera, respectively. This blocking ELISA is highly specific and offers many advantages over the current ELISAs that use inactivated FMDV antigen. This is the first report of the production and diagnostic application of recombinant pentameric subunits of FMDV. |
doi_str_mv | 10.1016/j.vaccine.2006.08.046 |
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The recombinant pentamer-like structures were produced in insect (Sf9) cells that were inoculated with recombinant baculoviruses that expressed, simultaneously, the genes for the P1 and 3C proteins of FMDV from individual promoters. The FMDV pentamer-like structures were processed by viral 3C protease, as shown in Western blots, and were antigenic, as revealed by their reactivities in an indirect ELISA. Analysis by CsCl gradient centrifugation showed that the pentamer-like structures were similar to authentic pentameric subunits from FMDV in terms of sedimentation velocity. Furthermore, the pentamer-like structures induced high levels of FMDV-specific antibodies in mice following immunization. Observations made under the electron microscope revealed that the pentamer-like structures expressed by insect cells self-assembled to form pentameric subunits of 7–8 nm in diameter, which resemble the authentic FMDV (23 ± 2 nm in diameter). The results indicate that these pentamer-like structures are as antigenic and immunogenic as authentic FMDV, although the former are smaller in size. Based on these results, a blocking ELISA was developed using the recombinant pentamer-like structure. The ELISA showed specificity of 99.5% and sensitivity of 98.5% when tested with FMDV antibody-negative and -positive sera, respectively. This blocking ELISA is highly specific and offers many advantages over the current ELISAs that use inactivated FMDV antigen. This is the first report of the production and diagnostic application of recombinant pentameric subunits of FMDV.</description><identifier>ISSN: 0264-410X</identifier><identifier>EISSN: 1873-2518</identifier><identifier>DOI: 10.1016/j.vaccine.2006.08.046</identifier><identifier>PMID: 17386963</identifier><identifier>CODEN: VACCDE</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Allergy and Immunology ; Animals ; Antigens ; Antigens, Viral - biosynthesis ; Antigens, Viral - genetics ; Antigens, Viral - immunology ; Applied microbiology ; Baculoviridae - genetics ; Baculoviridae - immunology ; Baculovirus ; Biological and medical sciences ; Blocking ELISA ; Cattle ; Centrifugation ; Cloning ; Enzyme-Linked Immunosorbent Assay - methods ; Enzymes ; Female ; Foot & mouth disease ; Foot-and-mouth disease virus ; Foot-and-Mouth Disease Virus - genetics ; Foot-and-Mouth Disease Virus - immunology ; Fundamental and applied biological sciences. Psychology ; Gene amplification ; Genomes ; Immunization ; Immunogenicity ; Infections ; Insects ; Laboratories ; Mice ; Mice, Inbred BALB C ; Microbiology ; Miscellaneous ; Pentameric subunits ; Plasmids ; Proteins ; Spodoptera - virology ; Swine ; Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects) ; Virology ; Viruses</subject><ispartof>Vaccine, 2007-05, Vol.25 (20), p.4112-4121</ispartof><rights>Elsevier Ltd</rights><rights>2007 Elsevier Ltd</rights><rights>2007 INIST-CNRS</rights><rights>Copyright Elsevier Limited May 16, 2007</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c507t-5432c10813f0917a43b7f18f27575475d9f5529c1c427fe2adfe158aa07a15723</citedby><cites>FETCH-LOGICAL-c507t-5432c10813f0917a43b7f18f27575475d9f5529c1c427fe2adfe158aa07a15723</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/1559083104?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994,64384,64386,64388,72240</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18739292$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17386963$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Oem, Jae-Ku</creatorcontrib><creatorcontrib>Park, Jong-Hyeon</creatorcontrib><creatorcontrib>Lee, Kwang-Nyeong</creatorcontrib><creatorcontrib>Kim, Yong-Joo</creatorcontrib><creatorcontrib>Kye, Soo-Jeong</creatorcontrib><creatorcontrib>Park, Jee-Yong</creatorcontrib><creatorcontrib>Song, Hee-Jong</creatorcontrib><title>Characterization of recombinant foot-and-mouth disease virus pentamer-like structures expressed by baculovirus and their use as diagnostic antigens in a blocking ELISA</title><title>Vaccine</title><addtitle>Vaccine</addtitle><description>Abstract Non-infectious recombinant pentamer-like structures of the foot-and-mouth disease virus (FMDV) were expressed by baculovirus, and the antigenicity and immunogenicity of the proteins were analyzed in a blocking ELISA for the detection of FMDV antibodies. The recombinant pentamer-like structures were produced in insect (Sf9) cells that were inoculated with recombinant baculoviruses that expressed, simultaneously, the genes for the P1 and 3C proteins of FMDV from individual promoters. The FMDV pentamer-like structures were processed by viral 3C protease, as shown in Western blots, and were antigenic, as revealed by their reactivities in an indirect ELISA. Analysis by CsCl gradient centrifugation showed that the pentamer-like structures were similar to authentic pentameric subunits from FMDV in terms of sedimentation velocity. Furthermore, the pentamer-like structures induced high levels of FMDV-specific antibodies in mice following immunization. Observations made under the electron microscope revealed that the pentamer-like structures expressed by insect cells self-assembled to form pentameric subunits of 7–8 nm in diameter, which resemble the authentic FMDV (23 ± 2 nm in diameter). The results indicate that these pentamer-like structures are as antigenic and immunogenic as authentic FMDV, although the former are smaller in size. Based on these results, a blocking ELISA was developed using the recombinant pentamer-like structure. The ELISA showed specificity of 99.5% and sensitivity of 98.5% when tested with FMDV antibody-negative and -positive sera, respectively. This blocking ELISA is highly specific and offers many advantages over the current ELISAs that use inactivated FMDV antigen. This is the first report of the production and diagnostic application of recombinant pentameric subunits of FMDV.</description><subject>Allergy and Immunology</subject><subject>Animals</subject><subject>Antigens</subject><subject>Antigens, Viral - biosynthesis</subject><subject>Antigens, Viral - genetics</subject><subject>Antigens, Viral - immunology</subject><subject>Applied microbiology</subject><subject>Baculoviridae - genetics</subject><subject>Baculoviridae - immunology</subject><subject>Baculovirus</subject><subject>Biological and medical sciences</subject><subject>Blocking ELISA</subject><subject>Cattle</subject><subject>Centrifugation</subject><subject>Cloning</subject><subject>Enzyme-Linked Immunosorbent Assay - methods</subject><subject>Enzymes</subject><subject>Female</subject><subject>Foot & mouth disease</subject><subject>Foot-and-mouth disease virus</subject><subject>Foot-and-Mouth Disease Virus - genetics</subject><subject>Foot-and-Mouth Disease Virus - immunology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene amplification</subject><subject>Genomes</subject><subject>Immunization</subject><subject>Immunogenicity</subject><subject>Infections</subject><subject>Insects</subject><subject>Laboratories</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Microbiology</subject><subject>Miscellaneous</subject><subject>Pentameric subunits</subject><subject>Plasmids</subject><subject>Proteins</subject><subject>Spodoptera - virology</subject><subject>Swine</subject><subject>Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects)</subject><subject>Virology</subject><subject>Viruses</subject><issn>0264-410X</issn><issn>1873-2518</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqFksGO0zAQhiMEYkvhEUCWENxSxnYcJxdWq2qBlVbisCBxs1xn0rpN7WI7FeWFeE1ctVKlvexpDvPNb8_8f1G8pTCjQOtP69leG2MdzhhAPYNmBlX9rJjQRvKSCdo8LybA6qqsKPy6Kl7FuAYAwWn7sriikjd1W_NJ8W--0kGbhMH-1cl6R3xPAhq_XVinXSK996nUriu3fkwr0tmIOiLZ2zBGskOX9BZDOdgNkpjCaNIYMBL8s8slYkcWB7LQZhz8aSIrkbRCG8iYVXTMgnrpfEzW5F6yS3SRWEc0WQzebKxbktv7u4eb18WLXg8R35zrtPj55fbH_Ft5__3r3fzmvjQCZCpFxZmh0FDeQ0ulrvhC9rTpmRRSVFJ0bS8Eaw01FZM9Mt31SEWjNUhNhWR8Wnw86e6C_z1iTGpro8Fh0A79GJWEircM5JMgA14D40fw_SNw7cfg8hKKCtFCw2nWnBbiRJngYwzYq12wWx0OioI6Gq7W6my4OhquoFHZ8Dz37qw-LrbYXabODmfgwxnQ0eihD9oZGy9cjkvL2uPi1ycO83X3FoOKxqIz2Nkch6Q6b5_8yudHCmawzuZHN3jAeNlaRaZAPRzTeQwnSMiHqir-H1IS4r8</recordid><startdate>20070516</startdate><enddate>20070516</enddate><creator>Oem, Jae-Ku</creator><creator>Park, Jong-Hyeon</creator><creator>Lee, Kwang-Nyeong</creator><creator>Kim, Yong-Joo</creator><creator>Kye, Soo-Jeong</creator><creator>Park, Jee-Yong</creator><creator>Song, Hee-Jong</creator><general>Elsevier Ltd</general><general>Elsevier</general><general>Elsevier Limited</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7RV</scope><scope>7T2</scope><scope>7T5</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88C</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0R</scope><scope>M0S</scope><scope>M0T</scope><scope>M1P</scope><scope>M2O</scope><scope>M7N</scope><scope>M7P</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20070516</creationdate><title>Characterization of recombinant foot-and-mouth disease virus pentamer-like structures expressed by baculovirus and their use as diagnostic antigens in a blocking ELISA</title><author>Oem, Jae-Ku ; Park, Jong-Hyeon ; Lee, Kwang-Nyeong ; Kim, Yong-Joo ; Kye, Soo-Jeong ; Park, Jee-Yong ; Song, Hee-Jong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c507t-5432c10813f0917a43b7f18f27575475d9f5529c1c427fe2adfe158aa07a15723</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Allergy and Immunology</topic><topic>Animals</topic><topic>Antigens</topic><topic>Antigens, Viral - biosynthesis</topic><topic>Antigens, Viral - genetics</topic><topic>Antigens, Viral - immunology</topic><topic>Applied microbiology</topic><topic>Baculoviridae - genetics</topic><topic>Baculoviridae - immunology</topic><topic>Baculovirus</topic><topic>Biological and medical sciences</topic><topic>Blocking ELISA</topic><topic>Cattle</topic><topic>Centrifugation</topic><topic>Cloning</topic><topic>Enzyme-Linked Immunosorbent Assay - methods</topic><topic>Enzymes</topic><topic>Female</topic><topic>Foot & mouth disease</topic><topic>Foot-and-mouth disease virus</topic><topic>Foot-and-Mouth Disease Virus - genetics</topic><topic>Foot-and-Mouth Disease Virus - immunology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene amplification</topic><topic>Genomes</topic><topic>Immunization</topic><topic>Immunogenicity</topic><topic>Infections</topic><topic>Insects</topic><topic>Laboratories</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Microbiology</topic><topic>Miscellaneous</topic><topic>Pentameric subunits</topic><topic>Plasmids</topic><topic>Proteins</topic><topic>Spodoptera - virology</topic><topic>Swine</topic><topic>Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects)</topic><topic>Virology</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Oem, Jae-Ku</creatorcontrib><creatorcontrib>Park, Jong-Hyeon</creatorcontrib><creatorcontrib>Lee, Kwang-Nyeong</creatorcontrib><creatorcontrib>Kim, Yong-Joo</creatorcontrib><creatorcontrib>Kye, Soo-Jeong</creatorcontrib><creatorcontrib>Park, Jee-Yong</creatorcontrib><creatorcontrib>Song, Hee-Jong</creatorcontrib><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>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Nursing & Allied Health Database</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Healthcare Administration Database (Alumni)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Healthcare Administration Database</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Vaccine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Oem, Jae-Ku</au><au>Park, Jong-Hyeon</au><au>Lee, Kwang-Nyeong</au><au>Kim, Yong-Joo</au><au>Kye, Soo-Jeong</au><au>Park, Jee-Yong</au><au>Song, Hee-Jong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characterization of recombinant foot-and-mouth disease virus pentamer-like structures expressed by baculovirus and their use as diagnostic antigens in a blocking ELISA</atitle><jtitle>Vaccine</jtitle><addtitle>Vaccine</addtitle><date>2007-05-16</date><risdate>2007</risdate><volume>25</volume><issue>20</issue><spage>4112</spage><epage>4121</epage><pages>4112-4121</pages><issn>0264-410X</issn><eissn>1873-2518</eissn><coden>VACCDE</coden><abstract>Abstract Non-infectious recombinant pentamer-like structures of the foot-and-mouth disease virus (FMDV) were expressed by baculovirus, and the antigenicity and immunogenicity of the proteins were analyzed in a blocking ELISA for the detection of FMDV antibodies. The recombinant pentamer-like structures were produced in insect (Sf9) cells that were inoculated with recombinant baculoviruses that expressed, simultaneously, the genes for the P1 and 3C proteins of FMDV from individual promoters. The FMDV pentamer-like structures were processed by viral 3C protease, as shown in Western blots, and were antigenic, as revealed by their reactivities in an indirect ELISA. Analysis by CsCl gradient centrifugation showed that the pentamer-like structures were similar to authentic pentameric subunits from FMDV in terms of sedimentation velocity. Furthermore, the pentamer-like structures induced high levels of FMDV-specific antibodies in mice following immunization. Observations made under the electron microscope revealed that the pentamer-like structures expressed by insect cells self-assembled to form pentameric subunits of 7–8 nm in diameter, which resemble the authentic FMDV (23 ± 2 nm in diameter). The results indicate that these pentamer-like structures are as antigenic and immunogenic as authentic FMDV, although the former are smaller in size. Based on these results, a blocking ELISA was developed using the recombinant pentamer-like structure. The ELISA showed specificity of 99.5% and sensitivity of 98.5% when tested with FMDV antibody-negative and -positive sera, respectively. This blocking ELISA is highly specific and offers many advantages over the current ELISAs that use inactivated FMDV antigen. This is the first report of the production and diagnostic application of recombinant pentameric subunits of FMDV.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>17386963</pmid><doi>10.1016/j.vaccine.2006.08.046</doi><tpages>10</tpages></addata></record> |
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subjects | Allergy and Immunology Animals Antigens Antigens, Viral - biosynthesis Antigens, Viral - genetics Antigens, Viral - immunology Applied microbiology Baculoviridae - genetics Baculoviridae - immunology Baculovirus Biological and medical sciences Blocking ELISA Cattle Centrifugation Cloning Enzyme-Linked Immunosorbent Assay - methods Enzymes Female Foot & mouth disease Foot-and-mouth disease virus Foot-and-Mouth Disease Virus - genetics Foot-and-Mouth Disease Virus - immunology Fundamental and applied biological sciences. Psychology Gene amplification Genomes Immunization Immunogenicity Infections Insects Laboratories Mice Mice, Inbred BALB C Microbiology Miscellaneous Pentameric subunits Plasmids Proteins Spodoptera - virology Swine Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects) Virology Viruses |
title | Characterization of recombinant foot-and-mouth disease virus pentamer-like structures expressed by baculovirus and their use as diagnostic antigens in a blocking ELISA |
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