Significance of genetic variation of PRRSV ORF5 in virus neutralization and molecular determinants corresponding to cross neutralization among PRRS viruses

A high rate of genetic and antigenic variability among porcine reproductive and respiratory syndrome viruses (PRRSVs) hampers effective prevention and control of the disease caused by PRRSV. The major envelope protein (GP5) encoded by the ORF5 of PRRSV has a critical role in inducing virus neutraliz...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Veterinary microbiology 2013-02, Vol.162 (1), p.10-22
Hauptverfasser: Kim, Won-Il, Kim, Jae-Jo, Cha, Sang-Ho, Wu, Wai-Hong, Cooper, Vickie, Evans, Rich, Choi, En-Jin, Yoon, Kyoung-Jin
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 22
container_issue 1
container_start_page 10
container_title Veterinary microbiology
container_volume 162
creator Kim, Won-Il
Kim, Jae-Jo
Cha, Sang-Ho
Wu, Wai-Hong
Cooper, Vickie
Evans, Rich
Choi, En-Jin
Yoon, Kyoung-Jin
description A high rate of genetic and antigenic variability among porcine reproductive and respiratory syndrome viruses (PRRSVs) hampers effective prevention and control of the disease caused by PRRSV. The major envelope protein (GP5) encoded by the ORF5 of PRRSV has a critical role in inducing virus neutralizing (VN) antibody and cross protection among different strains of PRRSV. This study was conducted to identify sequence elements related to cross neutralization by comparing the ORF5 sequences of 69 field isolates in conjunction with their susceptibility to VN antibody raised against the VR2332 strain in vitro and in vivo. Five common variable sites (amino acid position 32–34, 38–39, 57–59, 137 and 151) were identified between susceptible and resistant viral isolates. Mutants whose ORF5 amino acid sequences were substituted with the sequences corresponding to the 5 identified common variable sites individually or concurrently were generated from a VR2332-backboned infectious clone by site mutagenesis. The change in the susceptibility of the mutants to VN antibodies specific for VR2332 or a heterologous PRRSV was assessed to determine the association of those 5 identified sites with cross neutralization. Among the five sites, the changes of amino acid sequences at three sites (32–34, 38–39, and 57–59) located in the N-terminal ectodomain of ORF5 significantly influenced the susceptibility of the mutant viruses to VN antibody, suggesting that sequence homology at these sites can be utilized as genetic markers to predict the degree of cross neutralization among different PRRSVs.
doi_str_mv 10.1016/j.vetmic.2012.08.005
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1315609696</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0378113512004567</els_id><sourcerecordid>1315609696</sourcerecordid><originalsourceid>FETCH-LOGICAL-c419t-39dbdbf7c91cb4b9a3d71f0feda7f900e2103cae765fbd2fc5456f8363d91cc63</originalsourceid><addsrcrecordid>eNp9kc2KFDEUhYMoTjv6BqJZuqn2plKpn40gg6PCwEi34zakkpsmTVXSJqkGfRVf1qqp0Y3gKpB855x7cwh5yWDLgNVvj9sz5tHpbQms3EK7BRCPyIa1DS9KUZWPyQZ40xaMcXFBnqV0BICqq-EpuSjLTnQAzYb82ruDd9Zp5TXSYOkBPWan6VlFp7ILfrn8stvtv9Hb3bWgztOzi1OiHqcc1eB-rpTyho5hQD0NKlKDGePovPI5UR1ixHQK3jh_oDlQHUP612AM8-uStAZgek6eWDUkfPFwXpK76w9frz4VN7cfP1-9vyl0xbpc8M70preN7pjuq75T3DTMgkWjGjtviSUDrhU2tbC9Ka0Wlahty2tuZoWu-SV5s_qeYvg-YcpydEnjMCiPYUqScSZq6OpuQasVvV8hopWn6EYVf0gGcqlFHuVai1xqkdDKuZZZ9uohYepHNH9Ff3qYgdcrYFWQ6hBdknf72aECYK2o7pPfrQTOP3F2GGXSDufSjIuoszTB_X-G30Z6rfo</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1315609696</pqid></control><display><type>article</type><title>Significance of genetic variation of PRRSV ORF5 in virus neutralization and molecular determinants corresponding to cross neutralization among PRRS viruses</title><source>MEDLINE</source><source>ScienceDirect Journals (5 years ago - present)</source><creator>Kim, Won-Il ; Kim, Jae-Jo ; Cha, Sang-Ho ; Wu, Wai-Hong ; Cooper, Vickie ; Evans, Rich ; Choi, En-Jin ; Yoon, Kyoung-Jin</creator><creatorcontrib>Kim, Won-Il ; Kim, Jae-Jo ; Cha, Sang-Ho ; Wu, Wai-Hong ; Cooper, Vickie ; Evans, Rich ; Choi, En-Jin ; Yoon, Kyoung-Jin</creatorcontrib><description>A high rate of genetic and antigenic variability among porcine reproductive and respiratory syndrome viruses (PRRSVs) hampers effective prevention and control of the disease caused by PRRSV. The major envelope protein (GP5) encoded by the ORF5 of PRRSV has a critical role in inducing virus neutralizing (VN) antibody and cross protection among different strains of PRRSV. This study was conducted to identify sequence elements related to cross neutralization by comparing the ORF5 sequences of 69 field isolates in conjunction with their susceptibility to VN antibody raised against the VR2332 strain in vitro and in vivo. Five common variable sites (amino acid position 32–34, 38–39, 57–59, 137 and 151) were identified between susceptible and resistant viral isolates. Mutants whose ORF5 amino acid sequences were substituted with the sequences corresponding to the 5 identified common variable sites individually or concurrently were generated from a VR2332-backboned infectious clone by site mutagenesis. The change in the susceptibility of the mutants to VN antibodies specific for VR2332 or a heterologous PRRSV was assessed to determine the association of those 5 identified sites with cross neutralization. Among the five sites, the changes of amino acid sequences at three sites (32–34, 38–39, and 57–59) located in the N-terminal ectodomain of ORF5 significantly influenced the susceptibility of the mutant viruses to VN antibody, suggesting that sequence homology at these sites can be utilized as genetic markers to predict the degree of cross neutralization among different PRRSVs.</description><identifier>ISSN: 0378-1135</identifier><identifier>EISSN: 1873-2542</identifier><identifier>DOI: 10.1016/j.vetmic.2012.08.005</identifier><identifier>PMID: 22959007</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Amino Acid Sequence ; amino acid sequences ; amino acids ; Animals ; antibodies ; clones ; Cross neutralization ; Cross Reactions ; disease prevention ; Genetic marker ; genetic markers ; Genetic Variation ; Genotype ; Immunization, Passive ; Immunoglobulins - immunology ; Immunoglobulins - pharmacology ; Molecular Sequence Data ; mutagenesis ; Mutagenesis, Site-Directed ; mutants ; neutralization ; Neutralization Tests ; ORF5 ; porcine reproductive and respiratory syndrome ; Porcine Reproductive and Respiratory Syndrome - prevention &amp; control ; Porcine Reproductive and Respiratory Syndrome - virology ; Porcine reproductive and respiratory syndrome virus ; Porcine respiratory and reproductive syndrome virus ; Porcine respiratory and reproductive syndrome virus - genetics ; Porcine respiratory and reproductive syndrome virus - immunology ; Porcine respiratory and reproductive syndrome virus - isolation &amp; purification ; proteins ; PRRSV ; Sequence Alignment ; sequence homology ; Swine ; Viral Envelope Proteins - genetics ; Viral Envelope Proteins - immunology ; viruses</subject><ispartof>Veterinary microbiology, 2013-02, Vol.162 (1), p.10-22</ispartof><rights>2012 Elsevier B.V.</rights><rights>Copyright © 2012 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c419t-39dbdbf7c91cb4b9a3d71f0feda7f900e2103cae765fbd2fc5456f8363d91cc63</citedby><cites>FETCH-LOGICAL-c419t-39dbdbf7c91cb4b9a3d71f0feda7f900e2103cae765fbd2fc5456f8363d91cc63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0378113512004567$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22959007$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, Won-Il</creatorcontrib><creatorcontrib>Kim, Jae-Jo</creatorcontrib><creatorcontrib>Cha, Sang-Ho</creatorcontrib><creatorcontrib>Wu, Wai-Hong</creatorcontrib><creatorcontrib>Cooper, Vickie</creatorcontrib><creatorcontrib>Evans, Rich</creatorcontrib><creatorcontrib>Choi, En-Jin</creatorcontrib><creatorcontrib>Yoon, Kyoung-Jin</creatorcontrib><title>Significance of genetic variation of PRRSV ORF5 in virus neutralization and molecular determinants corresponding to cross neutralization among PRRS viruses</title><title>Veterinary microbiology</title><addtitle>Vet Microbiol</addtitle><description>A high rate of genetic and antigenic variability among porcine reproductive and respiratory syndrome viruses (PRRSVs) hampers effective prevention and control of the disease caused by PRRSV. The major envelope protein (GP5) encoded by the ORF5 of PRRSV has a critical role in inducing virus neutralizing (VN) antibody and cross protection among different strains of PRRSV. This study was conducted to identify sequence elements related to cross neutralization by comparing the ORF5 sequences of 69 field isolates in conjunction with their susceptibility to VN antibody raised against the VR2332 strain in vitro and in vivo. Five common variable sites (amino acid position 32–34, 38–39, 57–59, 137 and 151) were identified between susceptible and resistant viral isolates. Mutants whose ORF5 amino acid sequences were substituted with the sequences corresponding to the 5 identified common variable sites individually or concurrently were generated from a VR2332-backboned infectious clone by site mutagenesis. The change in the susceptibility of the mutants to VN antibodies specific for VR2332 or a heterologous PRRSV was assessed to determine the association of those 5 identified sites with cross neutralization. Among the five sites, the changes of amino acid sequences at three sites (32–34, 38–39, and 57–59) located in the N-terminal ectodomain of ORF5 significantly influenced the susceptibility of the mutant viruses to VN antibody, suggesting that sequence homology at these sites can be utilized as genetic markers to predict the degree of cross neutralization among different PRRSVs.</description><subject>Amino Acid Sequence</subject><subject>amino acid sequences</subject><subject>amino acids</subject><subject>Animals</subject><subject>antibodies</subject><subject>clones</subject><subject>Cross neutralization</subject><subject>Cross Reactions</subject><subject>disease prevention</subject><subject>Genetic marker</subject><subject>genetic markers</subject><subject>Genetic Variation</subject><subject>Genotype</subject><subject>Immunization, Passive</subject><subject>Immunoglobulins - immunology</subject><subject>Immunoglobulins - pharmacology</subject><subject>Molecular Sequence Data</subject><subject>mutagenesis</subject><subject>Mutagenesis, Site-Directed</subject><subject>mutants</subject><subject>neutralization</subject><subject>Neutralization Tests</subject><subject>ORF5</subject><subject>porcine reproductive and respiratory syndrome</subject><subject>Porcine Reproductive and Respiratory Syndrome - prevention &amp; control</subject><subject>Porcine Reproductive and Respiratory Syndrome - virology</subject><subject>Porcine reproductive and respiratory syndrome virus</subject><subject>Porcine respiratory and reproductive syndrome virus</subject><subject>Porcine respiratory and reproductive syndrome virus - genetics</subject><subject>Porcine respiratory and reproductive syndrome virus - immunology</subject><subject>Porcine respiratory and reproductive syndrome virus - isolation &amp; purification</subject><subject>proteins</subject><subject>PRRSV</subject><subject>Sequence Alignment</subject><subject>sequence homology</subject><subject>Swine</subject><subject>Viral Envelope Proteins - genetics</subject><subject>Viral Envelope Proteins - immunology</subject><subject>viruses</subject><issn>0378-1135</issn><issn>1873-2542</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc2KFDEUhYMoTjv6BqJZuqn2plKpn40gg6PCwEi34zakkpsmTVXSJqkGfRVf1qqp0Y3gKpB855x7cwh5yWDLgNVvj9sz5tHpbQms3EK7BRCPyIa1DS9KUZWPyQZ40xaMcXFBnqV0BICqq-EpuSjLTnQAzYb82ruDd9Zp5TXSYOkBPWan6VlFp7ILfrn8stvtv9Hb3bWgztOzi1OiHqcc1eB-rpTyho5hQD0NKlKDGePovPI5UR1ixHQK3jh_oDlQHUP612AM8-uStAZgek6eWDUkfPFwXpK76w9frz4VN7cfP1-9vyl0xbpc8M70preN7pjuq75T3DTMgkWjGjtviSUDrhU2tbC9Ka0Wlahty2tuZoWu-SV5s_qeYvg-YcpydEnjMCiPYUqScSZq6OpuQasVvV8hopWn6EYVf0gGcqlFHuVai1xqkdDKuZZZ9uohYepHNH9Ff3qYgdcrYFWQ6hBdknf72aECYK2o7pPfrQTOP3F2GGXSDufSjIuoszTB_X-G30Z6rfo</recordid><startdate>20130222</startdate><enddate>20130222</enddate><creator>Kim, Won-Il</creator><creator>Kim, Jae-Jo</creator><creator>Cha, Sang-Ho</creator><creator>Wu, Wai-Hong</creator><creator>Cooper, Vickie</creator><creator>Evans, Rich</creator><creator>Choi, En-Jin</creator><creator>Yoon, Kyoung-Jin</creator><general>Elsevier B.V</general><scope>FBQ</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>7U9</scope><scope>H94</scope></search><sort><creationdate>20130222</creationdate><title>Significance of genetic variation of PRRSV ORF5 in virus neutralization and molecular determinants corresponding to cross neutralization among PRRS viruses</title><author>Kim, Won-Il ; Kim, Jae-Jo ; Cha, Sang-Ho ; Wu, Wai-Hong ; Cooper, Vickie ; Evans, Rich ; Choi, En-Jin ; Yoon, Kyoung-Jin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c419t-39dbdbf7c91cb4b9a3d71f0feda7f900e2103cae765fbd2fc5456f8363d91cc63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Amino Acid Sequence</topic><topic>amino acid sequences</topic><topic>amino acids</topic><topic>Animals</topic><topic>antibodies</topic><topic>clones</topic><topic>Cross neutralization</topic><topic>Cross Reactions</topic><topic>disease prevention</topic><topic>Genetic marker</topic><topic>genetic markers</topic><topic>Genetic Variation</topic><topic>Genotype</topic><topic>Immunization, Passive</topic><topic>Immunoglobulins - immunology</topic><topic>Immunoglobulins - pharmacology</topic><topic>Molecular Sequence Data</topic><topic>mutagenesis</topic><topic>Mutagenesis, Site-Directed</topic><topic>mutants</topic><topic>neutralization</topic><topic>Neutralization Tests</topic><topic>ORF5</topic><topic>porcine reproductive and respiratory syndrome</topic><topic>Porcine Reproductive and Respiratory Syndrome - prevention &amp; control</topic><topic>Porcine Reproductive and Respiratory Syndrome - virology</topic><topic>Porcine reproductive and respiratory syndrome virus</topic><topic>Porcine respiratory and reproductive syndrome virus</topic><topic>Porcine respiratory and reproductive syndrome virus - genetics</topic><topic>Porcine respiratory and reproductive syndrome virus - immunology</topic><topic>Porcine respiratory and reproductive syndrome virus - isolation &amp; purification</topic><topic>proteins</topic><topic>PRRSV</topic><topic>Sequence Alignment</topic><topic>sequence homology</topic><topic>Swine</topic><topic>Viral Envelope Proteins - genetics</topic><topic>Viral Envelope Proteins - immunology</topic><topic>viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Won-Il</creatorcontrib><creatorcontrib>Kim, Jae-Jo</creatorcontrib><creatorcontrib>Cha, Sang-Ho</creatorcontrib><creatorcontrib>Wu, Wai-Hong</creatorcontrib><creatorcontrib>Cooper, Vickie</creatorcontrib><creatorcontrib>Evans, Rich</creatorcontrib><creatorcontrib>Choi, En-Jin</creatorcontrib><creatorcontrib>Yoon, Kyoung-Jin</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Veterinary microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Won-Il</au><au>Kim, Jae-Jo</au><au>Cha, Sang-Ho</au><au>Wu, Wai-Hong</au><au>Cooper, Vickie</au><au>Evans, Rich</au><au>Choi, En-Jin</au><au>Yoon, Kyoung-Jin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Significance of genetic variation of PRRSV ORF5 in virus neutralization and molecular determinants corresponding to cross neutralization among PRRS viruses</atitle><jtitle>Veterinary microbiology</jtitle><addtitle>Vet Microbiol</addtitle><date>2013-02-22</date><risdate>2013</risdate><volume>162</volume><issue>1</issue><spage>10</spage><epage>22</epage><pages>10-22</pages><issn>0378-1135</issn><eissn>1873-2542</eissn><abstract>A high rate of genetic and antigenic variability among porcine reproductive and respiratory syndrome viruses (PRRSVs) hampers effective prevention and control of the disease caused by PRRSV. The major envelope protein (GP5) encoded by the ORF5 of PRRSV has a critical role in inducing virus neutralizing (VN) antibody and cross protection among different strains of PRRSV. This study was conducted to identify sequence elements related to cross neutralization by comparing the ORF5 sequences of 69 field isolates in conjunction with their susceptibility to VN antibody raised against the VR2332 strain in vitro and in vivo. Five common variable sites (amino acid position 32–34, 38–39, 57–59, 137 and 151) were identified between susceptible and resistant viral isolates. Mutants whose ORF5 amino acid sequences were substituted with the sequences corresponding to the 5 identified common variable sites individually or concurrently were generated from a VR2332-backboned infectious clone by site mutagenesis. The change in the susceptibility of the mutants to VN antibodies specific for VR2332 or a heterologous PRRSV was assessed to determine the association of those 5 identified sites with cross neutralization. Among the five sites, the changes of amino acid sequences at three sites (32–34, 38–39, and 57–59) located in the N-terminal ectodomain of ORF5 significantly influenced the susceptibility of the mutant viruses to VN antibody, suggesting that sequence homology at these sites can be utilized as genetic markers to predict the degree of cross neutralization among different PRRSVs.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>22959007</pmid><doi>10.1016/j.vetmic.2012.08.005</doi><tpages>13</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0378-1135
ispartof Veterinary microbiology, 2013-02, Vol.162 (1), p.10-22
issn 0378-1135
1873-2542
language eng
recordid cdi_proquest_miscellaneous_1315609696
source MEDLINE; ScienceDirect Journals (5 years ago - present)
subjects Amino Acid Sequence
amino acid sequences
amino acids
Animals
antibodies
clones
Cross neutralization
Cross Reactions
disease prevention
Genetic marker
genetic markers
Genetic Variation
Genotype
Immunization, Passive
Immunoglobulins - immunology
Immunoglobulins - pharmacology
Molecular Sequence Data
mutagenesis
Mutagenesis, Site-Directed
mutants
neutralization
Neutralization Tests
ORF5
porcine reproductive and respiratory syndrome
Porcine Reproductive and Respiratory Syndrome - prevention & control
Porcine Reproductive and Respiratory Syndrome - virology
Porcine reproductive and respiratory syndrome virus
Porcine respiratory and reproductive syndrome virus
Porcine respiratory and reproductive syndrome virus - genetics
Porcine respiratory and reproductive syndrome virus - immunology
Porcine respiratory and reproductive syndrome virus - isolation & purification
proteins
PRRSV
Sequence Alignment
sequence homology
Swine
Viral Envelope Proteins - genetics
Viral Envelope Proteins - immunology
viruses
title Significance of genetic variation of PRRSV ORF5 in virus neutralization and molecular determinants corresponding to cross neutralization among PRRS viruses
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-01T19%3A13%3A17IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Significance%20of%20genetic%20variation%20of%20PRRSV%20ORF5%20in%20virus%20neutralization%20and%20molecular%20determinants%20corresponding%20to%20cross%20neutralization%20among%20PRRS%20viruses&rft.jtitle=Veterinary%20microbiology&rft.au=Kim,%20Won-Il&rft.date=2013-02-22&rft.volume=162&rft.issue=1&rft.spage=10&rft.epage=22&rft.pages=10-22&rft.issn=0378-1135&rft.eissn=1873-2542&rft_id=info:doi/10.1016/j.vetmic.2012.08.005&rft_dat=%3Cproquest_cross%3E1315609696%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1315609696&rft_id=info:pmid/22959007&rft_els_id=S0378113512004567&rfr_iscdi=true