Efficacy of a high potency O1 Manisa monovalent vaccine against heterologous challenge with a FMDV O Mya98 lineage virus in pigs 4 and 7 days post vaccination
Abstract Early protection with a high potency (>6PD50 ) foot-and-mouth disease (FMD) O1 Manisa (Middle-East South Asia lineage) vaccine against challenge with O/VIT/2010 (O Mya98 lineage) was tested in pigs. Only two pigs that were vaccinated seven days prior to challenge had any demonstrable ant...
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Veröffentlicht in: | Vaccine 2015-06, Vol.33 (24), p.2778-2785 |
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creator | Wilna, Vosloo Hong, Nguyen Thi Thu Geoffrey, Fosgate T Jacqueline, Morris Michelle Jianning, Wang Van Phuc, Kim Ngon, Quach Vo Phuong, Le Thi Thu Hung, Dang Hanh, Tran Xuan Van Hung, Vo Anh, Le Thi Quynh Tien, Mai Thi My Quang, Le Tin Vinh Long, Ngo Thanh Nagendrakumar, Singanallur Balasubramanian |
description | Abstract Early protection with a high potency (>6PD50 ) foot-and-mouth disease (FMD) O1 Manisa (Middle-East South Asia lineage) vaccine against challenge with O/VIT/2010 (O Mya98 lineage) was tested in pigs. Only two pigs that were vaccinated seven days prior to challenge had any demonstrable antibodies as a result of vaccination at the time of challenge. However, 80% and 60% of pigs that were vaccinated seven and four days prior to coronary band challenge were protected. Vaccination significantly reduced the amount of virus excreted in nasal swabs, saliva and faeces compared to unvaccinated and infected controls. Virus and viral RNA could be detected in some pigs until termination of the experiment 14 days after challenge. Antibodies to the non-structural proteins (NSP) were detected in only one pig that was challenged four days post vaccination (dpv) and transiently in two pigs that were challenged seven dpv at only one time point. For each vaccine and control group, a group of unvaccinated pigs were kept in the same room but with no direct contact with the infected pigs to determine whether vaccination prevented transmission. Despite the presence of live virus and viral RNA in these indirect contact pigs, the groups in contact with the vaccinated and infected pigs did not develop clinical signs nor did they sero-convert. Contact pigs in the same room as unvaccinated challenged controls did show signs of disease and virus infection that resulted in sero-conversion to the NSP. A breach of the wall that separated the two groups at nine days post challenge might have contributed to this finding. This study showed that high potency vaccine can provide protection to pigs soon after vaccination and that aerosol transmission within rooms is a rare event. |
doi_str_mv | 10.1016/j.vaccine.2015.04.045 |
format | Article |
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Only two pigs that were vaccinated seven days prior to challenge had any demonstrable antibodies as a result of vaccination at the time of challenge. However, 80% and 60% of pigs that were vaccinated seven and four days prior to coronary band challenge were protected. Vaccination significantly reduced the amount of virus excreted in nasal swabs, saliva and faeces compared to unvaccinated and infected controls. Virus and viral RNA could be detected in some pigs until termination of the experiment 14 days after challenge. Antibodies to the non-structural proteins (NSP) were detected in only one pig that was challenged four days post vaccination (dpv) and transiently in two pigs that were challenged seven dpv at only one time point. For each vaccine and control group, a group of unvaccinated pigs were kept in the same room but with no direct contact with the infected pigs to determine whether vaccination prevented transmission. Despite the presence of live virus and viral RNA in these indirect contact pigs, the groups in contact with the vaccinated and infected pigs did not develop clinical signs nor did they sero-convert. Contact pigs in the same room as unvaccinated challenged controls did show signs of disease and virus infection that resulted in sero-conversion to the NSP. A breach of the wall that separated the two groups at nine days post challenge might have contributed to this finding. This study showed that high potency vaccine can provide protection to pigs soon after vaccination and that aerosol transmission within rooms is a rare event.</description><identifier>ISSN: 0264-410X</identifier><identifier>EISSN: 1873-2518</identifier><identifier>DOI: 10.1016/j.vaccine.2015.04.045</identifier><identifier>PMID: 25917677</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Allergy and Immunology ; Animals ; Antibodies, Viral - immunology ; Early protection ; Feces - virology ; FMD vaccine ; Foot-and-Mouth Disease - prevention & control ; Foot-and-Mouth Disease - transmission ; Foot-and-mouth disease virus ; Foot-and-Mouth Disease Virus - genetics ; Foot-and-Mouth Disease Virus - immunology ; Foot-and-Mouth Disease Virus - isolation & purification ; Heterologous challenge ; High potency ; Pigs ; RNA, Viral - genetics ; RNA, Viral - isolation & purification ; Saliva - virology ; Sus scrofa - immunology ; Swine ; Swine Diseases - prevention & control ; Swine Diseases - virology ; Vaccination - veterinary ; Vaccine Potency ; Viral Vaccines - administration & dosage ; Viral Vaccines - immunology ; Viremia - virology</subject><ispartof>Vaccine, 2015-06, Vol.33 (24), p.2778-2785</ispartof><rights>The Authors</rights><rights>2015 The Authors</rights><rights>Copyright © 2015 The Authors. Published by Elsevier Ltd.. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4155-398a7455f022b963053947b510906ee514ec467f05e850d64d2b4e07b298a1b93</citedby><cites>FETCH-LOGICAL-c4155-398a7455f022b963053947b510906ee514ec467f05e850d64d2b4e07b298a1b93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.vaccine.2015.04.045$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,45974,64364</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25917677$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wilna, Vosloo</creatorcontrib><creatorcontrib>Hong, Nguyen Thi Thu</creatorcontrib><creatorcontrib>Geoffrey, Fosgate T</creatorcontrib><creatorcontrib>Jacqueline, Morris Michelle</creatorcontrib><creatorcontrib>Jianning, Wang</creatorcontrib><creatorcontrib>Van Phuc, Kim</creatorcontrib><creatorcontrib>Ngon, Quach Vo</creatorcontrib><creatorcontrib>Phuong, Le Thi Thu</creatorcontrib><creatorcontrib>Hung, Dang</creatorcontrib><creatorcontrib>Hanh, Tran Xuan</creatorcontrib><creatorcontrib>Van Hung, Vo</creatorcontrib><creatorcontrib>Anh, Le Thi Quynh</creatorcontrib><creatorcontrib>Tien, Mai Thi My</creatorcontrib><creatorcontrib>Quang, Le Tin Vinh</creatorcontrib><creatorcontrib>Long, Ngo Thanh</creatorcontrib><creatorcontrib>Nagendrakumar, Singanallur Balasubramanian</creatorcontrib><title>Efficacy of a high potency O1 Manisa monovalent vaccine against heterologous challenge with a FMDV O Mya98 lineage virus in pigs 4 and 7 days post vaccination</title><title>Vaccine</title><addtitle>Vaccine</addtitle><description>Abstract Early protection with a high potency (>6PD50 ) foot-and-mouth disease (FMD) O1 Manisa (Middle-East South Asia lineage) vaccine against challenge with O/VIT/2010 (O Mya98 lineage) was tested in pigs. Only two pigs that were vaccinated seven days prior to challenge had any demonstrable antibodies as a result of vaccination at the time of challenge. However, 80% and 60% of pigs that were vaccinated seven and four days prior to coronary band challenge were protected. Vaccination significantly reduced the amount of virus excreted in nasal swabs, saliva and faeces compared to unvaccinated and infected controls. Virus and viral RNA could be detected in some pigs until termination of the experiment 14 days after challenge. Antibodies to the non-structural proteins (NSP) were detected in only one pig that was challenged four days post vaccination (dpv) and transiently in two pigs that were challenged seven dpv at only one time point. For each vaccine and control group, a group of unvaccinated pigs were kept in the same room but with no direct contact with the infected pigs to determine whether vaccination prevented transmission. Despite the presence of live virus and viral RNA in these indirect contact pigs, the groups in contact with the vaccinated and infected pigs did not develop clinical signs nor did they sero-convert. Contact pigs in the same room as unvaccinated challenged controls did show signs of disease and virus infection that resulted in sero-conversion to the NSP. A breach of the wall that separated the two groups at nine days post challenge might have contributed to this finding. This study showed that high potency vaccine can provide protection to pigs soon after vaccination and that aerosol transmission within rooms is a rare event.</description><subject>Allergy and Immunology</subject><subject>Animals</subject><subject>Antibodies, Viral - immunology</subject><subject>Early protection</subject><subject>Feces - virology</subject><subject>FMD vaccine</subject><subject>Foot-and-Mouth Disease - prevention & control</subject><subject>Foot-and-Mouth Disease - transmission</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>Foot-and-Mouth Disease Virus - isolation & purification</subject><subject>Heterologous challenge</subject><subject>High potency</subject><subject>Pigs</subject><subject>RNA, Viral - genetics</subject><subject>RNA, Viral - isolation & purification</subject><subject>Saliva - virology</subject><subject>Sus scrofa - immunology</subject><subject>Swine</subject><subject>Swine Diseases - prevention & control</subject><subject>Swine Diseases - virology</subject><subject>Vaccination - veterinary</subject><subject>Vaccine Potency</subject><subject>Viral Vaccines - administration & dosage</subject><subject>Viral Vaccines - immunology</subject><subject>Viremia - virology</subject><issn>0264-410X</issn><issn>1873-2518</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNUk2P0zAQjRCILQs_AeQjlxSPYyfxBYSW_UDaqgc-xM1ynEnqktrFTovyZ_itOGqXAxeQRrLkeW-eZt7LspdAl0ChfLNdHrUx1uGSURBLylOJR9kC6qrImYD6cbagrOQ5B_rtInsW45ZSKgqQT7MLJiRUZVUtsl_XXWeNNhPxHdFkY_sN2fsRXfpZA1lpZ6MmO-_8UQ_oRnJWJbrX1sWRbHDE4Aff-0MkZqOHhOqR_LTjJs27WX34StZkNWlZkyHxdOodbUhY68je9pFwol1LKtLqKSbp-CChR-vd8-xJp4eIL87vZfbl5vrz1V1-v779ePX-PjcchMgLWeuKC9FRxhpZFmlPyatGAJW0RBTA0fCy6qjAWtC25C1rONKqYYkIjSwus9enufvgfxwwjmpno8Fh0A7TYgqqgtWFZPQ_oGUNEkqoRYKKE9QEH2PATu2D3ekwKaBqdlFt1fmeanZRUZ5q5r06SxyaHbZ_WA-2JcC7EwDTTY4Wg4rGJs-wtQHNqFpv_ynx9q8JJtmTkjB8xwnj1h-CSwdXoCJTVH2aozQnCUQKEZWi-A28uMQJ</recordid><startdate>20150604</startdate><enddate>20150604</enddate><creator>Wilna, Vosloo</creator><creator>Hong, Nguyen Thi Thu</creator><creator>Geoffrey, Fosgate T</creator><creator>Jacqueline, Morris Michelle</creator><creator>Jianning, Wang</creator><creator>Van Phuc, Kim</creator><creator>Ngon, Quach Vo</creator><creator>Phuong, Le Thi Thu</creator><creator>Hung, Dang</creator><creator>Hanh, Tran Xuan</creator><creator>Van Hung, Vo</creator><creator>Anh, Le Thi Quynh</creator><creator>Tien, Mai Thi My</creator><creator>Quang, Le Tin Vinh</creator><creator>Long, Ngo Thanh</creator><creator>Nagendrakumar, Singanallur Balasubramanian</creator><general>Elsevier Ltd</general><scope>6I.</scope><scope>AAFTH</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>7X8</scope><scope>7T5</scope><scope>7U9</scope><scope>H94</scope></search><sort><creationdate>20150604</creationdate><title>Efficacy of a high potency O1 Manisa monovalent vaccine against heterologous challenge with a FMDV O Mya98 lineage virus in pigs 4 and 7 days post vaccination</title><author>Wilna, Vosloo ; Hong, Nguyen Thi Thu ; Geoffrey, Fosgate T ; Jacqueline, Morris Michelle ; Jianning, Wang ; Van Phuc, Kim ; Ngon, Quach Vo ; Phuong, Le Thi Thu ; Hung, Dang ; Hanh, Tran Xuan ; Van Hung, Vo ; Anh, Le Thi Quynh ; Tien, Mai Thi My ; Quang, Le Tin Vinh ; Long, Ngo Thanh ; Nagendrakumar, Singanallur Balasubramanian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4155-398a7455f022b963053947b510906ee514ec467f05e850d64d2b4e07b298a1b93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Allergy and Immunology</topic><topic>Animals</topic><topic>Antibodies, Viral - immunology</topic><topic>Early protection</topic><topic>Feces - virology</topic><topic>FMD vaccine</topic><topic>Foot-and-Mouth Disease - prevention & control</topic><topic>Foot-and-Mouth Disease - transmission</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>Foot-and-Mouth Disease Virus - isolation & purification</topic><topic>Heterologous challenge</topic><topic>High potency</topic><topic>Pigs</topic><topic>RNA, Viral - genetics</topic><topic>RNA, Viral - isolation & purification</topic><topic>Saliva - virology</topic><topic>Sus scrofa - immunology</topic><topic>Swine</topic><topic>Swine Diseases - prevention & control</topic><topic>Swine Diseases - virology</topic><topic>Vaccination - veterinary</topic><topic>Vaccine Potency</topic><topic>Viral Vaccines - administration & dosage</topic><topic>Viral Vaccines - immunology</topic><topic>Viremia - virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wilna, Vosloo</creatorcontrib><creatorcontrib>Hong, Nguyen Thi Thu</creatorcontrib><creatorcontrib>Geoffrey, Fosgate T</creatorcontrib><creatorcontrib>Jacqueline, Morris Michelle</creatorcontrib><creatorcontrib>Jianning, Wang</creatorcontrib><creatorcontrib>Van Phuc, Kim</creatorcontrib><creatorcontrib>Ngon, Quach Vo</creatorcontrib><creatorcontrib>Phuong, Le Thi Thu</creatorcontrib><creatorcontrib>Hung, Dang</creatorcontrib><creatorcontrib>Hanh, Tran Xuan</creatorcontrib><creatorcontrib>Van Hung, Vo</creatorcontrib><creatorcontrib>Anh, Le Thi Quynh</creatorcontrib><creatorcontrib>Tien, Mai Thi My</creatorcontrib><creatorcontrib>Quang, Le Tin Vinh</creatorcontrib><creatorcontrib>Long, Ngo Thanh</creatorcontrib><creatorcontrib>Nagendrakumar, Singanallur Balasubramanian</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><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>Vaccine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wilna, Vosloo</au><au>Hong, Nguyen Thi Thu</au><au>Geoffrey, Fosgate T</au><au>Jacqueline, Morris Michelle</au><au>Jianning, Wang</au><au>Van Phuc, Kim</au><au>Ngon, Quach Vo</au><au>Phuong, Le Thi Thu</au><au>Hung, Dang</au><au>Hanh, Tran Xuan</au><au>Van Hung, Vo</au><au>Anh, Le Thi Quynh</au><au>Tien, Mai Thi My</au><au>Quang, Le Tin Vinh</au><au>Long, Ngo Thanh</au><au>Nagendrakumar, Singanallur Balasubramanian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Efficacy of a high potency O1 Manisa monovalent vaccine against heterologous challenge with a FMDV O Mya98 lineage virus in pigs 4 and 7 days post vaccination</atitle><jtitle>Vaccine</jtitle><addtitle>Vaccine</addtitle><date>2015-06-04</date><risdate>2015</risdate><volume>33</volume><issue>24</issue><spage>2778</spage><epage>2785</epage><pages>2778-2785</pages><issn>0264-410X</issn><eissn>1873-2518</eissn><abstract>Abstract Early protection with a high potency (>6PD50 ) foot-and-mouth disease (FMD) O1 Manisa (Middle-East South Asia lineage) vaccine against challenge with O/VIT/2010 (O Mya98 lineage) was tested in pigs. Only two pigs that were vaccinated seven days prior to challenge had any demonstrable antibodies as a result of vaccination at the time of challenge. However, 80% and 60% of pigs that were vaccinated seven and four days prior to coronary band challenge were protected. Vaccination significantly reduced the amount of virus excreted in nasal swabs, saliva and faeces compared to unvaccinated and infected controls. Virus and viral RNA could be detected in some pigs until termination of the experiment 14 days after challenge. Antibodies to the non-structural proteins (NSP) were detected in only one pig that was challenged four days post vaccination (dpv) and transiently in two pigs that were challenged seven dpv at only one time point. For each vaccine and control group, a group of unvaccinated pigs were kept in the same room but with no direct contact with the infected pigs to determine whether vaccination prevented transmission. Despite the presence of live virus and viral RNA in these indirect contact pigs, the groups in contact with the vaccinated and infected pigs did not develop clinical signs nor did they sero-convert. Contact pigs in the same room as unvaccinated challenged controls did show signs of disease and virus infection that resulted in sero-conversion to the NSP. A breach of the wall that separated the two groups at nine days post challenge might have contributed to this finding. This study showed that high potency vaccine can provide protection to pigs soon after vaccination and that aerosol transmission within rooms is a rare event.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>25917677</pmid><doi>10.1016/j.vaccine.2015.04.045</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Allergy and Immunology Animals Antibodies, Viral - immunology Early protection Feces - virology FMD vaccine Foot-and-Mouth Disease - prevention & control Foot-and-Mouth Disease - transmission Foot-and-mouth disease virus Foot-and-Mouth Disease Virus - genetics Foot-and-Mouth Disease Virus - immunology Foot-and-Mouth Disease Virus - isolation & purification Heterologous challenge High potency Pigs RNA, Viral - genetics RNA, Viral - isolation & purification Saliva - virology Sus scrofa - immunology Swine Swine Diseases - prevention & control Swine Diseases - virology Vaccination - veterinary Vaccine Potency Viral Vaccines - administration & dosage Viral Vaccines - immunology Viremia - virology |
title | Efficacy of a high potency O1 Manisa monovalent vaccine against heterologous challenge with a FMDV O Mya98 lineage virus in pigs 4 and 7 days post vaccination |
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