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
Hauptverfasser: 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
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container_end_page 2785
container_issue 24
container_start_page 2778
container_title Vaccine
container_volume 33
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
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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. 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control</subject><subject>Swine Diseases - virology</subject><subject>Vaccination - veterinary</subject><subject>Vaccine Potency</subject><subject>Viral Vaccines - administration &amp; 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 &amp; 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 &amp; purification</topic><topic>Heterologous challenge</topic><topic>High potency</topic><topic>Pigs</topic><topic>RNA, Viral - genetics</topic><topic>RNA, Viral - isolation &amp; purification</topic><topic>Saliva - virology</topic><topic>Sus scrofa - immunology</topic><topic>Swine</topic><topic>Swine Diseases - prevention &amp; control</topic><topic>Swine Diseases - virology</topic><topic>Vaccination - veterinary</topic><topic>Vaccine Potency</topic><topic>Viral Vaccines - administration &amp; 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 (&gt;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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