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Development of a Monoclonal Antibody Against Porcine CD163 SRCR5 Domain Which Partially Blocks Infection of PRRSV
Porcine reproductive and respiratory syndrome virus (PRRSV), which seriously endangers the world pig industry, invades host cells through receptor-mediated endocytosis involving clathrin. CD163 is an essential receptor for PRRSV during its infection of cells. The scavenger receptor cysteine-rich 5 (...
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Published in: | Frontiers in veterinary science 2020-11, Vol.7, p.597843-597843 |
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container_title | Frontiers in veterinary science |
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creator | Zhang, Yujiao Zhang, Kuan Zheng, Hao Liu, Changlong Jiang, Yifeng Du, Nannan Li, Liwei Li, Guoxin Yu, Lingxue Zhou, Yanjun Tong, Wu Zhao, Kuan Tong, Guangzhi Gao, Fei |
description | Porcine reproductive and respiratory syndrome virus (PRRSV), which seriously endangers the world pig industry, invades host cells through receptor-mediated endocytosis involving clathrin. CD163 is an essential receptor for PRRSV during its infection of cells. The scavenger receptor cysteine-rich 5 (SRCR5) domain of the CD163 molecule is necessary for PRRSV infection, and interacts with glycoproteins GP2a and GP4 of PRRSV, allowing the virus to infect the host cells. In this study, a monoclonal antibody (mAb) against the SRCR5-6 region of porcine CD163 was developed, and the target epitope of the mAb was determined as
497
TWGTVCDSDF
506
, which is directly adjacent to the ligand-binding pocket (LBP) domain (487-495aa) of CD163. Further study indicated that the mAb could partially block PRRSV infection of its target cells, pulmonary alveolar macrophages. The mAb developed in the study may provide a foundation of antiviral therapy for PRRSV. |
doi_str_mv | 10.3389/fvets.2020.597843 |
format | article |
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497
TWGTVCDSDF
506
, which is directly adjacent to the ligand-binding pocket (LBP) domain (487-495aa) of CD163. Further study indicated that the mAb could partially block PRRSV infection of its target cells, pulmonary alveolar macrophages. The mAb developed in the study may provide a foundation of antiviral therapy for PRRSV.</description><identifier>ISSN: 2297-1769</identifier><identifier>EISSN: 2297-1769</identifier><identifier>DOI: 10.3389/fvets.2020.597843</identifier><identifier>PMID: 33251273</identifier><language>eng</language><publisher>Frontiers Media S.A</publisher><subject>CD163 ; epitope ; monoclonal antibody ; PRRSV ; SRCR5 ; Veterinary Science</subject><ispartof>Frontiers in veterinary science, 2020-11, Vol.7, p.597843-597843</ispartof><rights>Copyright © 2020 Zhang, Zhang, Zheng, Liu, Jiang, Du, Li, Li, Yu, Zhou, Tong, Zhao, Tong and Gao. 2020 Zhang, Zhang, Zheng, Liu, Jiang, Du, Li, Li, Yu, Zhou, Tong, Zhao, Tong and Gao</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c442t-336d7c2bc59fc0658779992fe47fa9a06e8275e2636da0dfab5086f8302a89773</citedby><cites>FETCH-LOGICAL-c442t-336d7c2bc59fc0658779992fe47fa9a06e8275e2636da0dfab5086f8302a89773</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7674782/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7674782/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771</link.rule.ids></links><search><creatorcontrib>Zhang, Yujiao</creatorcontrib><creatorcontrib>Zhang, Kuan</creatorcontrib><creatorcontrib>Zheng, Hao</creatorcontrib><creatorcontrib>Liu, Changlong</creatorcontrib><creatorcontrib>Jiang, Yifeng</creatorcontrib><creatorcontrib>Du, Nannan</creatorcontrib><creatorcontrib>Li, Liwei</creatorcontrib><creatorcontrib>Li, Guoxin</creatorcontrib><creatorcontrib>Yu, Lingxue</creatorcontrib><creatorcontrib>Zhou, Yanjun</creatorcontrib><creatorcontrib>Tong, Wu</creatorcontrib><creatorcontrib>Zhao, Kuan</creatorcontrib><creatorcontrib>Tong, Guangzhi</creatorcontrib><creatorcontrib>Gao, Fei</creatorcontrib><title>Development of a Monoclonal Antibody Against Porcine CD163 SRCR5 Domain Which Partially Blocks Infection of PRRSV</title><title>Frontiers in veterinary science</title><description>Porcine reproductive and respiratory syndrome virus (PRRSV), which seriously endangers the world pig industry, invades host cells through receptor-mediated endocytosis involving clathrin. CD163 is an essential receptor for PRRSV during its infection of cells. The scavenger receptor cysteine-rich 5 (SRCR5) domain of the CD163 molecule is necessary for PRRSV infection, and interacts with glycoproteins GP2a and GP4 of PRRSV, allowing the virus to infect the host cells. In this study, a monoclonal antibody (mAb) against the SRCR5-6 region of porcine CD163 was developed, and the target epitope of the mAb was determined as
497
TWGTVCDSDF
506
, which is directly adjacent to the ligand-binding pocket (LBP) domain (487-495aa) of CD163. Further study indicated that the mAb could partially block PRRSV infection of its target cells, pulmonary alveolar macrophages. The mAb developed in the study may provide a foundation of antiviral therapy for PRRSV.</description><subject>CD163</subject><subject>epitope</subject><subject>monoclonal antibody</subject><subject>PRRSV</subject><subject>SRCR5</subject><subject>Veterinary Science</subject><issn>2297-1769</issn><issn>2297-1769</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVkVtvEzEQhVcIRKvSH8CbH3lJ8GV9e0EKCdBIRUQpl0dr1msnLl47XW8i5d9301SIPs1oztE3ozlV9Z7gKWNKf_QHN5QpxRRPuZaqZq-qS0q1nBAp9Ov_-ovqupR7jDHhtWQKv60uGKOcUMkuq4eFO7iYd51LA8oeAfqeU7YxJ4holobQ5PaIZhsIqQxolXsbkkPzBREM3a3na44WuRtF9Gcb7BatoB8CxHhEn2O2fwtaJu_sEHI6wVfr9d3vd9UbD7G46-d6Vf36-uXn_GZy--Pbcj67ndi6psOEMdFKSxvLtbdYcCWl1pp6V0sPGrBwikruqBh9gFsPDcdKeMUwBaWlZFfV8sxtM9ybXR866I8mQzBPg9xvzOlYG52pAWyjtdOesNpS1tCWcipaThRpoWlG1qcza7dvOtfa8Vk9xBfQl0oKW7PJByOFrKWiI-DDM6DPD3tXBtOFYl2MkFzeF0NrwSXnlOnRSs5W2-dSeuf_rSHYnJI3T8mbU_LmnDx7BAfFoIQ</recordid><startdate>20201105</startdate><enddate>20201105</enddate><creator>Zhang, Yujiao</creator><creator>Zhang, Kuan</creator><creator>Zheng, Hao</creator><creator>Liu, Changlong</creator><creator>Jiang, Yifeng</creator><creator>Du, Nannan</creator><creator>Li, Liwei</creator><creator>Li, Guoxin</creator><creator>Yu, Lingxue</creator><creator>Zhou, Yanjun</creator><creator>Tong, Wu</creator><creator>Zhao, Kuan</creator><creator>Tong, Guangzhi</creator><creator>Gao, Fei</creator><general>Frontiers Media S.A</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20201105</creationdate><title>Development of a Monoclonal Antibody Against Porcine CD163 SRCR5 Domain Which Partially Blocks Infection of PRRSV</title><author>Zhang, Yujiao ; Zhang, Kuan ; Zheng, Hao ; Liu, Changlong ; Jiang, Yifeng ; Du, Nannan ; Li, Liwei ; Li, Guoxin ; Yu, Lingxue ; Zhou, Yanjun ; Tong, Wu ; Zhao, Kuan ; Tong, Guangzhi ; Gao, Fei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c442t-336d7c2bc59fc0658779992fe47fa9a06e8275e2636da0dfab5086f8302a89773</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>CD163</topic><topic>epitope</topic><topic>monoclonal antibody</topic><topic>PRRSV</topic><topic>SRCR5</topic><topic>Veterinary Science</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Yujiao</creatorcontrib><creatorcontrib>Zhang, Kuan</creatorcontrib><creatorcontrib>Zheng, Hao</creatorcontrib><creatorcontrib>Liu, Changlong</creatorcontrib><creatorcontrib>Jiang, Yifeng</creatorcontrib><creatorcontrib>Du, Nannan</creatorcontrib><creatorcontrib>Li, Liwei</creatorcontrib><creatorcontrib>Li, Guoxin</creatorcontrib><creatorcontrib>Yu, Lingxue</creatorcontrib><creatorcontrib>Zhou, Yanjun</creatorcontrib><creatorcontrib>Tong, Wu</creatorcontrib><creatorcontrib>Zhao, Kuan</creatorcontrib><creatorcontrib>Tong, Guangzhi</creatorcontrib><creatorcontrib>Gao, Fei</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Frontiers in veterinary science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Yujiao</au><au>Zhang, Kuan</au><au>Zheng, Hao</au><au>Liu, Changlong</au><au>Jiang, Yifeng</au><au>Du, Nannan</au><au>Li, Liwei</au><au>Li, Guoxin</au><au>Yu, Lingxue</au><au>Zhou, Yanjun</au><au>Tong, Wu</au><au>Zhao, Kuan</au><au>Tong, Guangzhi</au><au>Gao, Fei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of a Monoclonal Antibody Against Porcine CD163 SRCR5 Domain Which Partially Blocks Infection of PRRSV</atitle><jtitle>Frontiers in veterinary science</jtitle><date>2020-11-05</date><risdate>2020</risdate><volume>7</volume><spage>597843</spage><epage>597843</epage><pages>597843-597843</pages><issn>2297-1769</issn><eissn>2297-1769</eissn><abstract>Porcine reproductive and respiratory syndrome virus (PRRSV), which seriously endangers the world pig industry, invades host cells through receptor-mediated endocytosis involving clathrin. CD163 is an essential receptor for PRRSV during its infection of cells. The scavenger receptor cysteine-rich 5 (SRCR5) domain of the CD163 molecule is necessary for PRRSV infection, and interacts with glycoproteins GP2a and GP4 of PRRSV, allowing the virus to infect the host cells. In this study, a monoclonal antibody (mAb) against the SRCR5-6 region of porcine CD163 was developed, and the target epitope of the mAb was determined as
497
TWGTVCDSDF
506
, which is directly adjacent to the ligand-binding pocket (LBP) domain (487-495aa) of CD163. Further study indicated that the mAb could partially block PRRSV infection of its target cells, pulmonary alveolar macrophages. The mAb developed in the study may provide a foundation of antiviral therapy for PRRSV.</abstract><pub>Frontiers Media S.A</pub><pmid>33251273</pmid><doi>10.3389/fvets.2020.597843</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | CD163 epitope monoclonal antibody PRRSV SRCR5 Veterinary Science |
title | Development of a Monoclonal Antibody Against Porcine CD163 SRCR5 Domain Which Partially Blocks Infection of PRRSV |
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