Reduction of foot-and-mouth disease (FMD) virus load in nasal excretions, saliva and exhaled air of vaccinated pigs following direct contact challenge
Abstract In future, a policy of “vaccinate-to-live” may be included in the repertoire of foot-and-mouth disease (FMD) control measures and in support of this approach, we have investigated the hypothesis that vaccine-induced reduction in virus replication and excretion from pigs can be correlated to...
Gespeichert in:
Veröffentlicht in: | Vaccine 2007-11, Vol.25 (45), p.7806-7817 |
---|---|
Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 7817 |
---|---|
container_issue | 45 |
container_start_page | 7806 |
container_title | Vaccine |
container_volume | 25 |
creator | Parida, S Fleming, L Oh, Y Mahapatra, M Hamblin, P Gloster, J Doel, C Gubbins, S Paton, D.J |
description | Abstract In future, a policy of “vaccinate-to-live” may be included in the repertoire of foot-and-mouth disease (FMD) control measures and in support of this approach, we have investigated the hypothesis that vaccine-induced reduction in virus replication and excretion from pigs can be correlated to the severity of clinical signs of FMD by measuring excretion of virus in natural secretions and aerosols. The other aims of this study were to verify the existence of sub-clinical infection in vaccinated pigs, to evaluate the correlation between this and seroconversion to foot-and-mouth disease virus (FMDV) non-structural protein antibodies and to re-examine the occurrence of FMDV persistence in the oro-pharynx of pigs. Therefore, pigs were vaccinated (O1 Manisa) and challenged (O1 UKG) in a manner calculated to produce a broad range of clinical outcomes and were monitored for a minimum of another 33 days post-challenge. Eighty-one percent of the early (10 days vaccinated) challenged pigs and 25% of the late (29 days vaccinated) challenged pigs were clinically infected and all other vaccinated pigs were sub-clinically infected. Although vaccination could not provide complete clinical or virological protection, it reduced the severity of the disease, virus excretion and production of non-structural FMDV antibodies in vaccinated and subsequently infected pigs. As hypothesised, vaccine-induced reduction of virus replication and excretion was found to be correlated to the severity of clinical disease. RNA copies, but no live virus was detected from the pharyngeal and soft palate tissues of a minority of vaccinated and infected pigs beyond the acute stage of the infection. |
doi_str_mv | 10.1016/j.vaccine.2007.08.058 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_68426018</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0264410X07009747</els_id><sourcerecordid>68426018</sourcerecordid><originalsourceid>FETCH-LOGICAL-c573t-72846c3faa4be23427dc904f4070f2aa8707c1edae641394fcff93b5939c7ceb3</originalsourceid><addsrcrecordid>eNqFktuKFDEQhhtR3HH1EZSArCjYbU7d6b5RZHVVWBE8gHehJl09mzGTjEn36L6Iz2uaGRjYm70qUnx_HfJXUTxmtGKUNa_W1Q6MsR4rTqmqaFvRur1TLFirRMlr1t4tFpQ3spSM_jwpHqS0ppTWgnX3ixOmOk6VoIvi31fsJzPa4EkYyBDCWILvy02YxivS24SQkDy_-PzuBdnZOCXiAvTEeuIhgSP410Sc1eklyW-7A5LlOX0FDnsCNs5l95PCmDNbu0q5jXPhj_Wr3CGiGYkJfoQ5ZplDv8KHxb0BXMJHh3ha_Lh4__38Y3n55cOn87eXpamVGEvFW9kYMQDIJXIhuepNR-UgqaIDB2gVVYZhD9hIJjo5mGHoxLLuRGeUwaU4LZ7t625j-D1hGvXGJoPOgccwJd20kjeUtbeCrGuEVI3M4NMb4DpM0eclNKvrljGlOMtUvadMDClFHPQ22g3Ea82onv3Va33wV8_-atrq7G_WPTlUn5Yb7I-qg6EZODsAkAy4IYI3Nh25jrM8apO5N3sO8-_uLEadjEVvcO-I7oO9dZTXNyoYZ73NTX_hNabj1jpxTfW3-RjnW8zW0E5JJf4DVibcNQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1558117721</pqid></control><display><type>article</type><title>Reduction of foot-and-mouth disease (FMD) virus load in nasal excretions, saliva and exhaled air of vaccinated pigs following direct contact challenge</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><source>ProQuest Central UK/Ireland</source><creator>Parida, S ; Fleming, L ; Oh, Y ; Mahapatra, M ; Hamblin, P ; Gloster, J ; Doel, C ; Gubbins, S ; Paton, D.J</creator><creatorcontrib>Parida, S ; Fleming, L ; Oh, Y ; Mahapatra, M ; Hamblin, P ; Gloster, J ; Doel, C ; Gubbins, S ; Paton, D.J</creatorcontrib><description>Abstract In future, a policy of “vaccinate-to-live” may be included in the repertoire of foot-and-mouth disease (FMD) control measures and in support of this approach, we have investigated the hypothesis that vaccine-induced reduction in virus replication and excretion from pigs can be correlated to the severity of clinical signs of FMD by measuring excretion of virus in natural secretions and aerosols. The other aims of this study were to verify the existence of sub-clinical infection in vaccinated pigs, to evaluate the correlation between this and seroconversion to foot-and-mouth disease virus (FMDV) non-structural protein antibodies and to re-examine the occurrence of FMDV persistence in the oro-pharynx of pigs. Therefore, pigs were vaccinated (O1 Manisa) and challenged (O1 UKG) in a manner calculated to produce a broad range of clinical outcomes and were monitored for a minimum of another 33 days post-challenge. Eighty-one percent of the early (10 days vaccinated) challenged pigs and 25% of the late (29 days vaccinated) challenged pigs were clinically infected and all other vaccinated pigs were sub-clinically infected. Although vaccination could not provide complete clinical or virological protection, it reduced the severity of the disease, virus excretion and production of non-structural FMDV antibodies in vaccinated and subsequently infected pigs. As hypothesised, vaccine-induced reduction of virus replication and excretion was found to be correlated to the severity of clinical disease. RNA copies, but no live virus was detected from the pharyngeal and soft palate tissues of a minority of vaccinated and infected pigs beyond the acute stage of the infection.</description><identifier>ISSN: 0264-410X</identifier><identifier>EISSN: 1873-2518</identifier><identifier>DOI: 10.1016/j.vaccine.2007.08.058</identifier><identifier>PMID: 17920730</identifier><identifier>CODEN: VACCDE</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Allergy and Immunology ; Animals ; Antibodies, Viral - blood ; Applied microbiology ; Biological and medical sciences ; Body Fluids ; Cattle ; Cotton ; Direct contact challenge ; Excretion ; FMD emergency vaccination ; FMD virus excretion ; Foot & mouth disease ; Foot-and-Mouth Disease - immunology ; Foot-and-Mouth Disease - prevention & control ; Foot-and-mouth disease virus ; Foot-and-Mouth Disease Virus - immunology ; Foot-and-Mouth Disease Virus - physiology ; Fundamental and applied biological sciences. Psychology ; Hogs ; Immunization ; Infections ; Microbiology ; Miscellaneous ; Nose ; Oropharynx - virology ; Saliva ; Swine ; Vaccination - veterinary ; Vaccines ; Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects) ; Viral Load ; Viral Vaccines - immunology ; Virology</subject><ispartof>Vaccine, 2007-11, Vol.25 (45), p.7806-7817</ispartof><rights>Elsevier Ltd</rights><rights>2007 Elsevier Ltd</rights><rights>2007 INIST-CNRS</rights><rights>Copyright Elsevier Limited Nov 7, 2007</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c573t-72846c3faa4be23427dc904f4070f2aa8707c1edae641394fcff93b5939c7ceb3</citedby><cites>FETCH-LOGICAL-c573t-72846c3faa4be23427dc904f4070f2aa8707c1edae641394fcff93b5939c7ceb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/1558117721?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>315,781,785,3551,27929,27930,46000,64390,64392,64394,72474</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19211966$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17920730$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Parida, S</creatorcontrib><creatorcontrib>Fleming, L</creatorcontrib><creatorcontrib>Oh, Y</creatorcontrib><creatorcontrib>Mahapatra, M</creatorcontrib><creatorcontrib>Hamblin, P</creatorcontrib><creatorcontrib>Gloster, J</creatorcontrib><creatorcontrib>Doel, C</creatorcontrib><creatorcontrib>Gubbins, S</creatorcontrib><creatorcontrib>Paton, D.J</creatorcontrib><title>Reduction of foot-and-mouth disease (FMD) virus load in nasal excretions, saliva and exhaled air of vaccinated pigs following direct contact challenge</title><title>Vaccine</title><addtitle>Vaccine</addtitle><description>Abstract In future, a policy of “vaccinate-to-live” may be included in the repertoire of foot-and-mouth disease (FMD) control measures and in support of this approach, we have investigated the hypothesis that vaccine-induced reduction in virus replication and excretion from pigs can be correlated to the severity of clinical signs of FMD by measuring excretion of virus in natural secretions and aerosols. The other aims of this study were to verify the existence of sub-clinical infection in vaccinated pigs, to evaluate the correlation between this and seroconversion to foot-and-mouth disease virus (FMDV) non-structural protein antibodies and to re-examine the occurrence of FMDV persistence in the oro-pharynx of pigs. Therefore, pigs were vaccinated (O1 Manisa) and challenged (O1 UKG) in a manner calculated to produce a broad range of clinical outcomes and were monitored for a minimum of another 33 days post-challenge. Eighty-one percent of the early (10 days vaccinated) challenged pigs and 25% of the late (29 days vaccinated) challenged pigs were clinically infected and all other vaccinated pigs were sub-clinically infected. Although vaccination could not provide complete clinical or virological protection, it reduced the severity of the disease, virus excretion and production of non-structural FMDV antibodies in vaccinated and subsequently infected pigs. As hypothesised, vaccine-induced reduction of virus replication and excretion was found to be correlated to the severity of clinical disease. RNA copies, but no live virus was detected from the pharyngeal and soft palate tissues of a minority of vaccinated and infected pigs beyond the acute stage of the infection.</description><subject>Allergy and Immunology</subject><subject>Animals</subject><subject>Antibodies, Viral - blood</subject><subject>Applied microbiology</subject><subject>Biological and medical sciences</subject><subject>Body Fluids</subject><subject>Cattle</subject><subject>Cotton</subject><subject>Direct contact challenge</subject><subject>Excretion</subject><subject>FMD emergency vaccination</subject><subject>FMD virus excretion</subject><subject>Foot & mouth disease</subject><subject>Foot-and-Mouth Disease - immunology</subject><subject>Foot-and-Mouth Disease - prevention & control</subject><subject>Foot-and-mouth disease virus</subject><subject>Foot-and-Mouth Disease Virus - immunology</subject><subject>Foot-and-Mouth Disease Virus - physiology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Hogs</subject><subject>Immunization</subject><subject>Infections</subject><subject>Microbiology</subject><subject>Miscellaneous</subject><subject>Nose</subject><subject>Oropharynx - virology</subject><subject>Saliva</subject><subject>Swine</subject><subject>Vaccination - veterinary</subject><subject>Vaccines</subject><subject>Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects)</subject><subject>Viral Load</subject><subject>Viral Vaccines - immunology</subject><subject>Virology</subject><issn>0264-410X</issn><issn>1873-2518</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqFktuKFDEQhhtR3HH1EZSArCjYbU7d6b5RZHVVWBE8gHehJl09mzGTjEn36L6Iz2uaGRjYm70qUnx_HfJXUTxmtGKUNa_W1Q6MsR4rTqmqaFvRur1TLFirRMlr1t4tFpQ3spSM_jwpHqS0ppTWgnX3ixOmOk6VoIvi31fsJzPa4EkYyBDCWILvy02YxivS24SQkDy_-PzuBdnZOCXiAvTEeuIhgSP410Sc1eklyW-7A5LlOX0FDnsCNs5l95PCmDNbu0q5jXPhj_Wr3CGiGYkJfoQ5ZplDv8KHxb0BXMJHh3ha_Lh4__38Y3n55cOn87eXpamVGEvFW9kYMQDIJXIhuepNR-UgqaIDB2gVVYZhD9hIJjo5mGHoxLLuRGeUwaU4LZ7t625j-D1hGvXGJoPOgccwJd20kjeUtbeCrGuEVI3M4NMb4DpM0eclNKvrljGlOMtUvadMDClFHPQ22g3Ea82onv3Va33wV8_-atrq7G_WPTlUn5Yb7I-qg6EZODsAkAy4IYI3Nh25jrM8apO5N3sO8-_uLEadjEVvcO-I7oO9dZTXNyoYZ73NTX_hNabj1jpxTfW3-RjnW8zW0E5JJf4DVibcNQ</recordid><startdate>20071107</startdate><enddate>20071107</enddate><creator>Parida, S</creator><creator>Fleming, L</creator><creator>Oh, Y</creator><creator>Mahapatra, M</creator><creator>Hamblin, P</creator><creator>Gloster, J</creator><creator>Doel, C</creator><creator>Gubbins, S</creator><creator>Paton, D.J</creator><general>Elsevier Ltd</general><general>Elsevier</general><general>Elsevier Limited</general><scope>IQODW</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>3V.</scope><scope>7QL</scope><scope>7RV</scope><scope>7T2</scope><scope>7T5</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88C</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0R</scope><scope>M0S</scope><scope>M0T</scope><scope>M1P</scope><scope>M2O</scope><scope>M7N</scope><scope>M7P</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20071107</creationdate><title>Reduction of foot-and-mouth disease (FMD) virus load in nasal excretions, saliva and exhaled air of vaccinated pigs following direct contact challenge</title><author>Parida, S ; Fleming, L ; Oh, Y ; Mahapatra, M ; Hamblin, P ; Gloster, J ; Doel, C ; Gubbins, S ; Paton, D.J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c573t-72846c3faa4be23427dc904f4070f2aa8707c1edae641394fcff93b5939c7ceb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Allergy and Immunology</topic><topic>Animals</topic><topic>Antibodies, Viral - blood</topic><topic>Applied microbiology</topic><topic>Biological and medical sciences</topic><topic>Body Fluids</topic><topic>Cattle</topic><topic>Cotton</topic><topic>Direct contact challenge</topic><topic>Excretion</topic><topic>FMD emergency vaccination</topic><topic>FMD virus excretion</topic><topic>Foot & mouth disease</topic><topic>Foot-and-Mouth Disease - immunology</topic><topic>Foot-and-Mouth Disease - prevention & control</topic><topic>Foot-and-mouth disease virus</topic><topic>Foot-and-Mouth Disease Virus - immunology</topic><topic>Foot-and-Mouth Disease Virus - physiology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Hogs</topic><topic>Immunization</topic><topic>Infections</topic><topic>Microbiology</topic><topic>Miscellaneous</topic><topic>Nose</topic><topic>Oropharynx - virology</topic><topic>Saliva</topic><topic>Swine</topic><topic>Vaccination - veterinary</topic><topic>Vaccines</topic><topic>Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects)</topic><topic>Viral Load</topic><topic>Viral Vaccines - immunology</topic><topic>Virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Parida, S</creatorcontrib><creatorcontrib>Fleming, L</creatorcontrib><creatorcontrib>Oh, Y</creatorcontrib><creatorcontrib>Mahapatra, M</creatorcontrib><creatorcontrib>Hamblin, P</creatorcontrib><creatorcontrib>Gloster, J</creatorcontrib><creatorcontrib>Doel, C</creatorcontrib><creatorcontrib>Gubbins, S</creatorcontrib><creatorcontrib>Paton, D.J</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Nursing & Allied Health Database</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Healthcare Administration Database (Alumni)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection (ProQuest)</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Healthcare Administration Database</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Vaccine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Parida, S</au><au>Fleming, L</au><au>Oh, Y</au><au>Mahapatra, M</au><au>Hamblin, P</au><au>Gloster, J</au><au>Doel, C</au><au>Gubbins, S</au><au>Paton, D.J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reduction of foot-and-mouth disease (FMD) virus load in nasal excretions, saliva and exhaled air of vaccinated pigs following direct contact challenge</atitle><jtitle>Vaccine</jtitle><addtitle>Vaccine</addtitle><date>2007-11-07</date><risdate>2007</risdate><volume>25</volume><issue>45</issue><spage>7806</spage><epage>7817</epage><pages>7806-7817</pages><issn>0264-410X</issn><eissn>1873-2518</eissn><coden>VACCDE</coden><abstract>Abstract In future, a policy of “vaccinate-to-live” may be included in the repertoire of foot-and-mouth disease (FMD) control measures and in support of this approach, we have investigated the hypothesis that vaccine-induced reduction in virus replication and excretion from pigs can be correlated to the severity of clinical signs of FMD by measuring excretion of virus in natural secretions and aerosols. The other aims of this study were to verify the existence of sub-clinical infection in vaccinated pigs, to evaluate the correlation between this and seroconversion to foot-and-mouth disease virus (FMDV) non-structural protein antibodies and to re-examine the occurrence of FMDV persistence in the oro-pharynx of pigs. Therefore, pigs were vaccinated (O1 Manisa) and challenged (O1 UKG) in a manner calculated to produce a broad range of clinical outcomes and were monitored for a minimum of another 33 days post-challenge. Eighty-one percent of the early (10 days vaccinated) challenged pigs and 25% of the late (29 days vaccinated) challenged pigs were clinically infected and all other vaccinated pigs were sub-clinically infected. Although vaccination could not provide complete clinical or virological protection, it reduced the severity of the disease, virus excretion and production of non-structural FMDV antibodies in vaccinated and subsequently infected pigs. As hypothesised, vaccine-induced reduction of virus replication and excretion was found to be correlated to the severity of clinical disease. RNA copies, but no live virus was detected from the pharyngeal and soft palate tissues of a minority of vaccinated and infected pigs beyond the acute stage of the infection.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>17920730</pmid><doi>10.1016/j.vaccine.2007.08.058</doi><tpages>12</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0264-410X |
ispartof | Vaccine, 2007-11, Vol.25 (45), p.7806-7817 |
issn | 0264-410X 1873-2518 |
language | eng |
recordid | cdi_proquest_miscellaneous_68426018 |
source | MEDLINE; Access via ScienceDirect (Elsevier); ProQuest Central UK/Ireland |
subjects | Allergy and Immunology Animals Antibodies, Viral - blood Applied microbiology Biological and medical sciences Body Fluids Cattle Cotton Direct contact challenge Excretion FMD emergency vaccination FMD virus excretion Foot & mouth disease Foot-and-Mouth Disease - immunology Foot-and-Mouth Disease - prevention & control Foot-and-mouth disease virus Foot-and-Mouth Disease Virus - immunology Foot-and-Mouth Disease Virus - physiology Fundamental and applied biological sciences. Psychology Hogs Immunization Infections Microbiology Miscellaneous Nose Oropharynx - virology Saliva Swine Vaccination - veterinary Vaccines Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects) Viral Load Viral Vaccines - immunology Virology |
title | Reduction of foot-and-mouth disease (FMD) virus load in nasal excretions, saliva and exhaled air of vaccinated pigs following direct contact challenge |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-12T07%3A33%3A35IST&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=Reduction%20of%20foot-and-mouth%20disease%20(FMD)%20virus%20load%20in%20nasal%20excretions,%20saliva%20and%20exhaled%20air%20of%20vaccinated%20pigs%20following%20direct%20contact%20challenge&rft.jtitle=Vaccine&rft.au=Parida,%20S&rft.date=2007-11-07&rft.volume=25&rft.issue=45&rft.spage=7806&rft.epage=7817&rft.pages=7806-7817&rft.issn=0264-410X&rft.eissn=1873-2518&rft.coden=VACCDE&rft_id=info:doi/10.1016/j.vaccine.2007.08.058&rft_dat=%3Cproquest_cross%3E68426018%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=1558117721&rft_id=info:pmid/17920730&rft_els_id=S0264410X07009747&rfr_iscdi=true |