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Detection of highly pathogenic avian influenza virus infection in vaccinated chicken flocks by monitoring antibodies against non-structural protein 1 (NS1)
H5 and H7 highly pathogenic avian influenza virus (HPAIV) represent a major global concern in poultries and human health. Avian influenza (AI) vaccines are available but not preferred for field applications, primarily because vaccination interferes with sero-surveillances of AIV infection. To overco...
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Published in: | Veterinary microbiology 2011-01, Vol.147 (3), p.283-291 |
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creator | Takeyama, Natsumi Minari, Kenji Kajihara, Masahiro Isoda, Norikazu Sakamoto, Ryuichi Sasaki, Takashi Kokumai, Norihide Takikawa, Noriyasu Shiraishi, Rikiya Mase, Masaji Hagiwara, Junko Kodama, Toshiaki Imamura, Takashi Sakaguchi, Masashi Ohgitani, Toshiaki Sawata, Akira Okamatsu, Masatoshi Muramatsu, Masatake Tsukamoto, Kenji Lin, Zhifeng Tuchiya, Kotaro Sakoda, Yoshihiro Kida, Hiroshi |
description | H5 and H7 highly pathogenic avian influenza virus (HPAIV) represent a major global concern in poultries and human health. Avian influenza (AI) vaccines are available but not preferred for field applications, primarily because vaccination interferes with sero-surveillances of AIV infection. To overcome the problem, ELISA systems using non-structural protein 1 (NS1) of AIV as antigens (NS1-ELISA) have been developed to measure anti-NS1 antibodies that are raised in AIV-infected but not in vaccinated chickens. However, some AI-vaccinated chickens having a weak anti-virus immune response may subsequently be infected with AIV and spread the virus. This raises a concern for the validity of NS1-ELISA to detect AIV infection in previously vaccinated chickens. In this study, we developed NS1-ELISA and assessed its feasibility to detect HPAIV infection in chickens previously immunized with H5 or H7 AI vaccines. The results indicated that the NS1-ELISA could identify HPAIV infection in both unvaccinated and vaccinated chickens at 1 week after infection in correlation with results from time-consuming virus isolation tests. Taken together, the NS1-ELISA system would be valuable tool to define HPAIV infection when AI vaccine program is in place. |
doi_str_mv | 10.1016/j.vetmic.2010.07.002 |
format | article |
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Avian influenza (AI) vaccines are available but not preferred for field applications, primarily because vaccination interferes with sero-surveillances of AIV infection. To overcome the problem, ELISA systems using non-structural protein 1 (NS1) of AIV as antigens (NS1-ELISA) have been developed to measure anti-NS1 antibodies that are raised in AIV-infected but not in vaccinated chickens. However, some AI-vaccinated chickens having a weak anti-virus immune response may subsequently be infected with AIV and spread the virus. This raises a concern for the validity of NS1-ELISA to detect AIV infection in previously vaccinated chickens. In this study, we developed NS1-ELISA and assessed its feasibility to detect HPAIV infection in chickens previously immunized with H5 or H7 AI vaccines. The results indicated that the NS1-ELISA could identify HPAIV infection in both unvaccinated and vaccinated chickens at 1 week after infection in correlation with results from time-consuming virus isolation tests. Taken together, the NS1-ELISA system would be valuable tool to define HPAIV infection when AI vaccine program is in place.</description><identifier>ISSN: 0378-1135</identifier><identifier>EISSN: 1873-2542</identifier><identifier>DOI: 10.1016/j.vetmic.2010.07.002</identifier><identifier>PMID: 20673616</identifier><identifier>CODEN: VMICDQ</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>accuracy ; Animals ; antibodies ; Antibodies, Viral - blood ; Applied microbiology ; Avian influenza ; Avian influenza virus ; Biological and medical sciences ; Chickens ; disease surveillance ; disease transmission ; DIVA system ; enzyme-linked immunosorbent assay ; Enzyme-Linked Immunosorbent Assay - veterinary ; Fundamental and applied biological sciences. Psychology ; hemagglutinins ; highly pathogenic avian influenza virus ; immune response ; immunologic techniques ; Influenza A virus ; Influenza A virus - immunology ; Influenza in Birds - diagnosis ; Influenza in Birds - immunology ; Influenza in Birds - virology ; Influenza Vaccines - immunology ; Microbiology ; Miscellaneous ; nonstructural protein 1 ; NS1-ELISA ; pathogenicity ; Poultry Diseases - diagnosis ; Poultry Diseases - immunology ; Poultry Diseases - virology ; seroprevalence ; strains ; test sensitivity ; vaccination ; Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects) ; viral antigens ; Viral Nonstructural Proteins - immunology ; viral proteins ; Virology</subject><ispartof>Veterinary microbiology, 2011-01, Vol.147 (3), p.283-291</ispartof><rights>2010 Elsevier B.V.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2010 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c447t-ddac055f6eadfbfb3ccd52732dc52b6e4ca65078d801479d7f0a3602f80507b13</citedby><cites>FETCH-LOGICAL-c447t-ddac055f6eadfbfb3ccd52732dc52b6e4ca65078d801479d7f0a3602f80507b13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23746659$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20673616$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Takeyama, Natsumi</creatorcontrib><creatorcontrib>Minari, Kenji</creatorcontrib><creatorcontrib>Kajihara, Masahiro</creatorcontrib><creatorcontrib>Isoda, Norikazu</creatorcontrib><creatorcontrib>Sakamoto, Ryuichi</creatorcontrib><creatorcontrib>Sasaki, Takashi</creatorcontrib><creatorcontrib>Kokumai, Norihide</creatorcontrib><creatorcontrib>Takikawa, Noriyasu</creatorcontrib><creatorcontrib>Shiraishi, Rikiya</creatorcontrib><creatorcontrib>Mase, Masaji</creatorcontrib><creatorcontrib>Hagiwara, Junko</creatorcontrib><creatorcontrib>Kodama, Toshiaki</creatorcontrib><creatorcontrib>Imamura, Takashi</creatorcontrib><creatorcontrib>Sakaguchi, Masashi</creatorcontrib><creatorcontrib>Ohgitani, Toshiaki</creatorcontrib><creatorcontrib>Sawata, Akira</creatorcontrib><creatorcontrib>Okamatsu, Masatoshi</creatorcontrib><creatorcontrib>Muramatsu, Masatake</creatorcontrib><creatorcontrib>Tsukamoto, Kenji</creatorcontrib><creatorcontrib>Lin, Zhifeng</creatorcontrib><creatorcontrib>Tuchiya, Kotaro</creatorcontrib><creatorcontrib>Sakoda, Yoshihiro</creatorcontrib><creatorcontrib>Kida, Hiroshi</creatorcontrib><title>Detection of highly pathogenic avian influenza virus infection in vaccinated chicken flocks by monitoring antibodies against non-structural protein 1 (NS1)</title><title>Veterinary microbiology</title><addtitle>Vet Microbiol</addtitle><description>H5 and H7 highly pathogenic avian influenza virus (HPAIV) represent a major global concern in poultries and human health. Avian influenza (AI) vaccines are available but not preferred for field applications, primarily because vaccination interferes with sero-surveillances of AIV infection. To overcome the problem, ELISA systems using non-structural protein 1 (NS1) of AIV as antigens (NS1-ELISA) have been developed to measure anti-NS1 antibodies that are raised in AIV-infected but not in vaccinated chickens. However, some AI-vaccinated chickens having a weak anti-virus immune response may subsequently be infected with AIV and spread the virus. This raises a concern for the validity of NS1-ELISA to detect AIV infection in previously vaccinated chickens. In this study, we developed NS1-ELISA and assessed its feasibility to detect HPAIV infection in chickens previously immunized with H5 or H7 AI vaccines. The results indicated that the NS1-ELISA could identify HPAIV infection in both unvaccinated and vaccinated chickens at 1 week after infection in correlation with results from time-consuming virus isolation tests. Taken together, the NS1-ELISA system would be valuable tool to define HPAIV infection when AI vaccine program is in place.</description><subject>accuracy</subject><subject>Animals</subject><subject>antibodies</subject><subject>Antibodies, Viral - blood</subject><subject>Applied microbiology</subject><subject>Avian influenza</subject><subject>Avian influenza virus</subject><subject>Biological and medical sciences</subject><subject>Chickens</subject><subject>disease surveillance</subject><subject>disease transmission</subject><subject>DIVA system</subject><subject>enzyme-linked immunosorbent assay</subject><subject>Enzyme-Linked Immunosorbent Assay - veterinary</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>hemagglutinins</subject><subject>highly pathogenic avian influenza virus</subject><subject>immune response</subject><subject>immunologic techniques</subject><subject>Influenza A virus</subject><subject>Influenza A virus - immunology</subject><subject>Influenza in Birds - diagnosis</subject><subject>Influenza in Birds - immunology</subject><subject>Influenza in Birds - virology</subject><subject>Influenza Vaccines - immunology</subject><subject>Microbiology</subject><subject>Miscellaneous</subject><subject>nonstructural protein 1</subject><subject>NS1-ELISA</subject><subject>pathogenicity</subject><subject>Poultry Diseases - diagnosis</subject><subject>Poultry Diseases - immunology</subject><subject>Poultry Diseases - virology</subject><subject>seroprevalence</subject><subject>strains</subject><subject>test sensitivity</subject><subject>vaccination</subject><subject>Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects)</subject><subject>viral antigens</subject><subject>Viral Nonstructural Proteins - immunology</subject><subject>viral proteins</subject><subject>Virology</subject><issn>0378-1135</issn><issn>1873-2542</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNqFkU2P0zAQhiMEYpeFf4DAFwQcUsZOYicXJLR8Sis4LHu2HH-0003tru1UKn-FP4urFrjByfLoeWdG81TVUwoLCpS_WS92Nm9QLxiUEogFALtXndNeNDXrWna_OodG9DWlTXdWPUppDQDtwOFhdcaAi4ZTfl79fG-z1RmDJ8GRFS5X055sVV6FpfWoidqh8gS9m2brfyiywzinw_8UQk92Smv0KltD9Ar1rfXETUHfJjLuySZ4zCGiXxLlM47BoE1ELRX6lIkPvk45zjrPUU1kG0O2pSMlr75e09ePqwdOTck-Ob0X1c3HD98vP9dX3z59uXx3Veu2Fbk2RmnoOsetMm50Y6O16ZhomNEdG7ltteIdiN70QFsxGOFANRyY66GUR9pcVC-Pfcv8u9mmLDeYtJ0m5W2Yk-wFZx0MTft_ktFuEGxghWyPpI4hpWid3EbcqLiXFOTBn1zLoz958CdByOKvxJ6dBszjxpo_od_CCvDiBKik1eSi8hrTX64RLefdULjnR86pINUyFubmukxqgJbtGINCvD0Stpx2hzbKpNF6bQ3GIleagP_e9RdZrsb9</recordid><startdate>20110127</startdate><enddate>20110127</enddate><creator>Takeyama, Natsumi</creator><creator>Minari, Kenji</creator><creator>Kajihara, Masahiro</creator><creator>Isoda, Norikazu</creator><creator>Sakamoto, Ryuichi</creator><creator>Sasaki, Takashi</creator><creator>Kokumai, Norihide</creator><creator>Takikawa, Noriyasu</creator><creator>Shiraishi, Rikiya</creator><creator>Mase, Masaji</creator><creator>Hagiwara, Junko</creator><creator>Kodama, Toshiaki</creator><creator>Imamura, Takashi</creator><creator>Sakaguchi, Masashi</creator><creator>Ohgitani, Toshiaki</creator><creator>Sawata, Akira</creator><creator>Okamatsu, Masatoshi</creator><creator>Muramatsu, Masatake</creator><creator>Tsukamoto, Kenji</creator><creator>Lin, Zhifeng</creator><creator>Tuchiya, Kotaro</creator><creator>Sakoda, Yoshihiro</creator><creator>Kida, Hiroshi</creator><general>Elsevier B.V</general><general>Amsterdam; New York: Elsevier</general><general>Elsevier</general><scope>FBQ</scope><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>7X8</scope><scope>7U9</scope><scope>H94</scope></search><sort><creationdate>20110127</creationdate><title>Detection of highly pathogenic avian influenza virus infection in vaccinated chicken flocks by monitoring antibodies against non-structural protein 1 (NS1)</title><author>Takeyama, Natsumi ; Minari, Kenji ; Kajihara, Masahiro ; Isoda, Norikazu ; Sakamoto, Ryuichi ; Sasaki, Takashi ; Kokumai, Norihide ; Takikawa, Noriyasu ; Shiraishi, Rikiya ; Mase, Masaji ; Hagiwara, Junko ; Kodama, Toshiaki ; Imamura, Takashi ; Sakaguchi, Masashi ; Ohgitani, Toshiaki ; Sawata, Akira ; Okamatsu, Masatoshi ; Muramatsu, Masatake ; Tsukamoto, Kenji ; Lin, Zhifeng ; Tuchiya, Kotaro ; Sakoda, Yoshihiro ; Kida, Hiroshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c447t-ddac055f6eadfbfb3ccd52732dc52b6e4ca65078d801479d7f0a3602f80507b13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>accuracy</topic><topic>Animals</topic><topic>antibodies</topic><topic>Antibodies, Viral - blood</topic><topic>Applied microbiology</topic><topic>Avian influenza</topic><topic>Avian influenza virus</topic><topic>Biological and medical sciences</topic><topic>Chickens</topic><topic>disease surveillance</topic><topic>disease transmission</topic><topic>DIVA system</topic><topic>enzyme-linked immunosorbent assay</topic><topic>Enzyme-Linked Immunosorbent Assay - veterinary</topic><topic>Fundamental and applied biological sciences. 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Avian influenza (AI) vaccines are available but not preferred for field applications, primarily because vaccination interferes with sero-surveillances of AIV infection. To overcome the problem, ELISA systems using non-structural protein 1 (NS1) of AIV as antigens (NS1-ELISA) have been developed to measure anti-NS1 antibodies that are raised in AIV-infected but not in vaccinated chickens. However, some AI-vaccinated chickens having a weak anti-virus immune response may subsequently be infected with AIV and spread the virus. This raises a concern for the validity of NS1-ELISA to detect AIV infection in previously vaccinated chickens. In this study, we developed NS1-ELISA and assessed its feasibility to detect HPAIV infection in chickens previously immunized with H5 or H7 AI vaccines. The results indicated that the NS1-ELISA could identify HPAIV infection in both unvaccinated and vaccinated chickens at 1 week after infection in correlation with results from time-consuming virus isolation tests. Taken together, the NS1-ELISA system would be valuable tool to define HPAIV infection when AI vaccine program is in place.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>20673616</pmid><doi>10.1016/j.vetmic.2010.07.002</doi><tpages>9</tpages></addata></record> |
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subjects | accuracy Animals antibodies Antibodies, Viral - blood Applied microbiology Avian influenza Avian influenza virus Biological and medical sciences Chickens disease surveillance disease transmission DIVA system enzyme-linked immunosorbent assay Enzyme-Linked Immunosorbent Assay - veterinary Fundamental and applied biological sciences. Psychology hemagglutinins highly pathogenic avian influenza virus immune response immunologic techniques Influenza A virus Influenza A virus - immunology Influenza in Birds - diagnosis Influenza in Birds - immunology Influenza in Birds - virology Influenza Vaccines - immunology Microbiology Miscellaneous nonstructural protein 1 NS1-ELISA pathogenicity Poultry Diseases - diagnosis Poultry Diseases - immunology Poultry Diseases - virology seroprevalence strains test sensitivity vaccination Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects) viral antigens Viral Nonstructural Proteins - immunology viral proteins Virology |
title | Detection of highly pathogenic avian influenza virus infection in vaccinated chicken flocks by monitoring antibodies against non-structural protein 1 (NS1) |
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