Development of neutralizing monoclonal antibodies against VP4 of rotavirus CC0812-1
The G10P[15] rotavirus CC0812-1 isolated from a diarrheal woman in Wuhan, China, in 2008 is phylogenetically close to the Lanzhou lamb rotavirus (LLR) of a monovalent human rotavirus vaccine produced by the Lanzhou Institute of Biological Products, China, and rotavirus Lamb-NT. This rotavirus can be...
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Veröffentlicht in: | Hybridoma (2005) 2012-08, Vol.31 (4), p.279-283 |
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creator | Yang, Jihong Wang, Sanying Tian, Lin Zhang, Lei Li, Bing Dong, Changyuan Liu, Zhonglai Qi, Chao |
description | The G10P[15] rotavirus CC0812-1 isolated from a diarrheal woman in Wuhan, China, in 2008 is phylogenetically close to the Lanzhou lamb rotavirus (LLR) of a monovalent human rotavirus vaccine produced by the Lanzhou Institute of Biological Products, China, and rotavirus Lamb-NT. This rotavirus can be used as the backbone of the attenuated rotavirus reassortant as a rotavirus vaccine candidate. In this study, rotavirus CC0812-1 was purified from the culture supernatant of CC0812-1-infected MA104 cells and used as antigen to immunize BALB/c mice. Four hybridoma clones were developed secreting antibodies that reacted with CC0812-1, designated as 1B1, 1B8, 1F11, and 1G10, respectively. Western blot analysis indicated that the four monoclonal antibodies (MAbs) were all specific for VP4 of rotavirus CC0812-1. Isotyping revealed that MAbs 1B1, 1B8, and 1G10 belonged to the IgM class, while MAb 1F11 belonged to the IgG1 subclass. A neutralization test demonstrated that the four MAbs all had the capacity to neutralize rotavirus CC0812-1. The neutralizing titers of the BALB/c mice ascites were 1:2048, 1:1024, 1:512, and 1:512 for MAbs 1B1, 1B8, 1F11, and 1G10, respectively. |
doi_str_mv | 10.1089/hyb.2012.0016 |
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This rotavirus can be used as the backbone of the attenuated rotavirus reassortant as a rotavirus vaccine candidate. In this study, rotavirus CC0812-1 was purified from the culture supernatant of CC0812-1-infected MA104 cells and used as antigen to immunize BALB/c mice. Four hybridoma clones were developed secreting antibodies that reacted with CC0812-1, designated as 1B1, 1B8, 1F11, and 1G10, respectively. Western blot analysis indicated that the four monoclonal antibodies (MAbs) were all specific for VP4 of rotavirus CC0812-1. Isotyping revealed that MAbs 1B1, 1B8, and 1G10 belonged to the IgM class, while MAb 1F11 belonged to the IgG1 subclass. A neutralization test demonstrated that the four MAbs all had the capacity to neutralize rotavirus CC0812-1. The neutralizing titers of the BALB/c mice ascites were 1:2048, 1:1024, 1:512, and 1:512 for MAbs 1B1, 1B8, 1F11, and 1G10, respectively.</description><identifier>ISSN: 1554-0014</identifier><identifier>EISSN: 1557-8348</identifier><identifier>DOI: 10.1089/hyb.2012.0016</identifier><identifier>PMID: 22894782</identifier><language>eng</language><publisher>United States</publisher><subject>Animals ; Antibodies, Monoclonal, Murine-Derived - biosynthesis ; Antibodies, Monoclonal, Murine-Derived - immunology ; Antibodies, Neutralizing - biosynthesis ; Antibodies, Neutralizing - immunology ; Capsid - immunology ; Capsid - ultrastructure ; Capsid Proteins - immunology ; Cell Line ; Female ; Human rotavirus ; Hybridomas ; Immunoglobulin G - biosynthesis ; Immunoglobulin G - immunology ; Immunoglobulin M - biosynthesis ; Immunoglobulin M - immunology ; Mice ; Mice, Inbred BALB C ; Rotavirus - immunology ; Rotavirus - ultrastructure</subject><ispartof>Hybridoma (2005), 2012-08, Vol.31 (4), p.279-283</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c359t-c59632c18cd4260c0e30e34abab0b6128597d00481599adaf7f80099b2eb84073</citedby><cites>FETCH-LOGICAL-c359t-c59632c18cd4260c0e30e34abab0b6128597d00481599adaf7f80099b2eb84073</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22894782$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yang, Jihong</creatorcontrib><creatorcontrib>Wang, Sanying</creatorcontrib><creatorcontrib>Tian, Lin</creatorcontrib><creatorcontrib>Zhang, Lei</creatorcontrib><creatorcontrib>Li, Bing</creatorcontrib><creatorcontrib>Dong, Changyuan</creatorcontrib><creatorcontrib>Liu, Zhonglai</creatorcontrib><creatorcontrib>Qi, Chao</creatorcontrib><title>Development of neutralizing monoclonal antibodies against VP4 of rotavirus CC0812-1</title><title>Hybridoma (2005)</title><addtitle>Hybridoma (Larchmt)</addtitle><description>The G10P[15] rotavirus CC0812-1 isolated from a diarrheal woman in Wuhan, China, in 2008 is phylogenetically close to the Lanzhou lamb rotavirus (LLR) of a monovalent human rotavirus vaccine produced by the Lanzhou Institute of Biological Products, China, and rotavirus Lamb-NT. This rotavirus can be used as the backbone of the attenuated rotavirus reassortant as a rotavirus vaccine candidate. In this study, rotavirus CC0812-1 was purified from the culture supernatant of CC0812-1-infected MA104 cells and used as antigen to immunize BALB/c mice. Four hybridoma clones were developed secreting antibodies that reacted with CC0812-1, designated as 1B1, 1B8, 1F11, and 1G10, respectively. Western blot analysis indicated that the four monoclonal antibodies (MAbs) were all specific for VP4 of rotavirus CC0812-1. Isotyping revealed that MAbs 1B1, 1B8, and 1G10 belonged to the IgM class, while MAb 1F11 belonged to the IgG1 subclass. A neutralization test demonstrated that the four MAbs all had the capacity to neutralize rotavirus CC0812-1. The neutralizing titers of the BALB/c mice ascites were 1:2048, 1:1024, 1:512, and 1:512 for MAbs 1B1, 1B8, 1F11, and 1G10, respectively.</description><subject>Animals</subject><subject>Antibodies, Monoclonal, Murine-Derived - biosynthesis</subject><subject>Antibodies, Monoclonal, Murine-Derived - immunology</subject><subject>Antibodies, Neutralizing - biosynthesis</subject><subject>Antibodies, Neutralizing - immunology</subject><subject>Capsid - immunology</subject><subject>Capsid - ultrastructure</subject><subject>Capsid Proteins - immunology</subject><subject>Cell Line</subject><subject>Female</subject><subject>Human rotavirus</subject><subject>Hybridomas</subject><subject>Immunoglobulin G - biosynthesis</subject><subject>Immunoglobulin G - immunology</subject><subject>Immunoglobulin M - biosynthesis</subject><subject>Immunoglobulin M - immunology</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Rotavirus - immunology</subject><subject>Rotavirus - ultrastructure</subject><issn>1554-0014</issn><issn>1557-8348</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkctLxDAQh4Mo7rp69Co9euk6ebRNjlKfsKDg41qSNF0jbbI27cL619u6q1eFgRmGb36H-RA6xTDHwMXF20bNCWAyB8DpHpriJMliThnf_55ZPOzZBB2F8A5AU06yQzQhhAuWcTJFT1dmbWq_aozrIl9FzvRdK2v7ad0yarzzuvZO1pF0nVW-tCZEcimtC130-sjGi9Z3cm3bPkR5DhyTGB-jg0rWwZzs-gy93Fw_53fx4uH2Pr9cxJomoot1IlJKNOa6ZCQFDYYOxaSSClSKCU9EVgIwjhMhZCmrrOIAQihiFGeQ0Rk63-auWv_Rm9AVjQ3a1LV0xvehwJRQjtPhS_9EgTP6NwqUESCQJgMab1Hd-hBaUxWr1jay3QxQMdopBjvFaKcY7Qz82S66V40pf-kfHfQLH2eIMg</recordid><startdate>201208</startdate><enddate>201208</enddate><creator>Yang, Jihong</creator><creator>Wang, Sanying</creator><creator>Tian, Lin</creator><creator>Zhang, Lei</creator><creator>Li, Bing</creator><creator>Dong, Changyuan</creator><creator>Liu, Zhonglai</creator><creator>Qi, Chao</creator><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>7X8</scope><scope>7T5</scope><scope>7U9</scope><scope>H94</scope></search><sort><creationdate>201208</creationdate><title>Development of neutralizing monoclonal antibodies against VP4 of rotavirus CC0812-1</title><author>Yang, Jihong ; Wang, Sanying ; Tian, Lin ; Zhang, Lei ; Li, Bing ; Dong, Changyuan ; Liu, Zhonglai ; Qi, Chao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c359t-c59632c18cd4260c0e30e34abab0b6128597d00481599adaf7f80099b2eb84073</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Animals</topic><topic>Antibodies, Monoclonal, Murine-Derived - biosynthesis</topic><topic>Antibodies, Monoclonal, Murine-Derived - immunology</topic><topic>Antibodies, Neutralizing - biosynthesis</topic><topic>Antibodies, Neutralizing - immunology</topic><topic>Capsid - immunology</topic><topic>Capsid - ultrastructure</topic><topic>Capsid Proteins - immunology</topic><topic>Cell Line</topic><topic>Female</topic><topic>Human rotavirus</topic><topic>Hybridomas</topic><topic>Immunoglobulin G - biosynthesis</topic><topic>Immunoglobulin G - immunology</topic><topic>Immunoglobulin M - biosynthesis</topic><topic>Immunoglobulin M - immunology</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Rotavirus - immunology</topic><topic>Rotavirus - ultrastructure</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Jihong</creatorcontrib><creatorcontrib>Wang, Sanying</creatorcontrib><creatorcontrib>Tian, Lin</creatorcontrib><creatorcontrib>Zhang, Lei</creatorcontrib><creatorcontrib>Li, Bing</creatorcontrib><creatorcontrib>Dong, Changyuan</creatorcontrib><creatorcontrib>Liu, Zhonglai</creatorcontrib><creatorcontrib>Qi, Chao</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Hybridoma (2005)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Jihong</au><au>Wang, Sanying</au><au>Tian, Lin</au><au>Zhang, Lei</au><au>Li, Bing</au><au>Dong, Changyuan</au><au>Liu, Zhonglai</au><au>Qi, Chao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of neutralizing monoclonal antibodies against VP4 of rotavirus CC0812-1</atitle><jtitle>Hybridoma (2005)</jtitle><addtitle>Hybridoma (Larchmt)</addtitle><date>2012-08</date><risdate>2012</risdate><volume>31</volume><issue>4</issue><spage>279</spage><epage>283</epage><pages>279-283</pages><issn>1554-0014</issn><eissn>1557-8348</eissn><abstract>The G10P[15] rotavirus CC0812-1 isolated from a diarrheal woman in Wuhan, China, in 2008 is phylogenetically close to the Lanzhou lamb rotavirus (LLR) of a monovalent human rotavirus vaccine produced by the Lanzhou Institute of Biological Products, China, and rotavirus Lamb-NT. This rotavirus can be used as the backbone of the attenuated rotavirus reassortant as a rotavirus vaccine candidate. In this study, rotavirus CC0812-1 was purified from the culture supernatant of CC0812-1-infected MA104 cells and used as antigen to immunize BALB/c mice. Four hybridoma clones were developed secreting antibodies that reacted with CC0812-1, designated as 1B1, 1B8, 1F11, and 1G10, respectively. Western blot analysis indicated that the four monoclonal antibodies (MAbs) were all specific for VP4 of rotavirus CC0812-1. Isotyping revealed that MAbs 1B1, 1B8, and 1G10 belonged to the IgM class, while MAb 1F11 belonged to the IgG1 subclass. A neutralization test demonstrated that the four MAbs all had the capacity to neutralize rotavirus CC0812-1. The neutralizing titers of the BALB/c mice ascites were 1:2048, 1:1024, 1:512, and 1:512 for MAbs 1B1, 1B8, 1F11, and 1G10, respectively.</abstract><cop>United States</cop><pmid>22894782</pmid><doi>10.1089/hyb.2012.0016</doi><tpages>5</tpages></addata></record> |
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subjects | Animals Antibodies, Monoclonal, Murine-Derived - biosynthesis Antibodies, Monoclonal, Murine-Derived - immunology Antibodies, Neutralizing - biosynthesis Antibodies, Neutralizing - immunology Capsid - immunology Capsid - ultrastructure Capsid Proteins - immunology Cell Line Female Human rotavirus Hybridomas Immunoglobulin G - biosynthesis Immunoglobulin G - immunology Immunoglobulin M - biosynthesis Immunoglobulin M - immunology Mice Mice, Inbred BALB C Rotavirus - immunology Rotavirus - ultrastructure |
title | Development of neutralizing monoclonal antibodies against VP4 of rotavirus CC0812-1 |
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