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- Publisher Website: 10.1007/s00705-009-0425-6
- Scopus: eid_2-s2.0-70349569546
- PMID: 19543688
- WOS: WOS:000269687400003
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Article: Generation and evaluation of an H9N1 influenza vaccine derived by reverse genetics that allows utilization of a DIVA strategy for control of H9N2 avian influenza
Title | Generation and evaluation of an H9N1 influenza vaccine derived by reverse genetics that allows utilization of a DIVA strategy for control of H9N2 avian influenza | ||||||||||||||
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Authors | |||||||||||||||
Issue Date | 2009 | ||||||||||||||
Publisher | Springer Wien. The Journal's web site is located at http://www.springer.com/springerwiennewyork/medicine/journal/705 | ||||||||||||||
Citation | Archives Of Virology, 2009, v. 154 n. 8, p. 1203-1210 How to Cite? | ||||||||||||||
Abstract | H9N2 avian influenza viruses have circulated widely in domestic poultry around the world, and their outbreaks have resulted in heavy morbidity and mortality. In addition, H9N2 avian influenza viruses were transmitted directly from birds to humans in Hong Kong and mainland China during 1998 and 2003, which prompted the public health authorities to seek protective strategies to control H9N2 influenza viruses. In this study, we attempted to develop a DIVA (differentiating infected and vaccinated animals) strategy for H9N2 avian influenza viruses. This strategy does not interfere with serological monitoring and allows effective control of H9N2 avian influenza. We generated a reassortant H9N1 influenza vaccine strain by reverse genetics and employed an enzyme-linked immunosorbent assay (ELISA) with a truncated N1 antigen expressed in E. coli to differentiate between vaccinated and naturally infected animals. Immunization of BALB/c mice with the inactivated reassortant H9N1 vaccine conferred protection against lethal challenge with H9N2 viruses. Meanwhile, the ELISA can be used to distinguish between vaccination and natural infection quickly and easily. Therefore, this study has opened up a new avenue for the control of H9N2 avian influenza. © Springer-Verlag 2009. | ||||||||||||||
Persistent Identifier | http://hdl.handle.net/10722/142414 | ||||||||||||||
ISSN | 2023 Impact Factor: 2.5 2023 SCImago Journal Rankings: 0.590 | ||||||||||||||
ISI Accession Number ID |
Funding Information: We thank R. G. Webster ( from St. Jude Children's Research Hospital, Memphis, TN) for the pHW2000 plasmid. This study was supported by the following research funds: European Union project (SP5B-CT-2006-044161); National 973 Project (2005CB523007, 2006CB933102); Chinese Academy of Sciences (KSCX1-YW-R-14); Hunan Provincial Science and Technology Department (2006NK2003); National Key Technology R& D Program of China (2006BAD06A03); Science and Technology Commission of Shanghai Municipality ( 064319030). | ||||||||||||||
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Wu, R | en_HK |
dc.contributor.author | Chen, Q | en_HK |
dc.contributor.author | Zheng, L | en_HK |
dc.contributor.author | Chen, J | en_HK |
dc.contributor.author | Sui, Z | en_HK |
dc.contributor.author | Guan, Y | en_HK |
dc.contributor.author | Chen, Z | en_HK |
dc.date.accessioned | 2011-10-28T02:45:32Z | - |
dc.date.available | 2011-10-28T02:45:32Z | - |
dc.date.issued | 2009 | en_HK |
dc.identifier.citation | Archives Of Virology, 2009, v. 154 n. 8, p. 1203-1210 | en_HK |
dc.identifier.issn | 0304-8608 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/142414 | - |
dc.description.abstract | H9N2 avian influenza viruses have circulated widely in domestic poultry around the world, and their outbreaks have resulted in heavy morbidity and mortality. In addition, H9N2 avian influenza viruses were transmitted directly from birds to humans in Hong Kong and mainland China during 1998 and 2003, which prompted the public health authorities to seek protective strategies to control H9N2 influenza viruses. In this study, we attempted to develop a DIVA (differentiating infected and vaccinated animals) strategy for H9N2 avian influenza viruses. This strategy does not interfere with serological monitoring and allows effective control of H9N2 avian influenza. We generated a reassortant H9N1 influenza vaccine strain by reverse genetics and employed an enzyme-linked immunosorbent assay (ELISA) with a truncated N1 antigen expressed in E. coli to differentiate between vaccinated and naturally infected animals. Immunization of BALB/c mice with the inactivated reassortant H9N1 vaccine conferred protection against lethal challenge with H9N2 viruses. Meanwhile, the ELISA can be used to distinguish between vaccination and natural infection quickly and easily. Therefore, this study has opened up a new avenue for the control of H9N2 avian influenza. © Springer-Verlag 2009. | en_HK |
dc.language | eng | en_US |
dc.publisher | Springer Wien. The Journal's web site is located at http://www.springer.com/springerwiennewyork/medicine/journal/705 | en_HK |
dc.relation.ispartof | Archives of Virology | en_HK |
dc.rights | The original publication is available at www.springerlink.com | - |
dc.subject.mesh | Influenza A Virus, H9N2 Subtype - immunology | - |
dc.subject.mesh | Influenza Vaccines - administration and dosage - immunology | - |
dc.subject.mesh | Influenza in Birds - immunology - prevention and control | - |
dc.subject.mesh | Influenza, Human - immunology - prevention and control | - |
dc.subject.mesh | Orthomyxoviridae Infections - immunology - prevention and control | - |
dc.title | Generation and evaluation of an H9N1 influenza vaccine derived by reverse genetics that allows utilization of a DIVA strategy for control of H9N2 avian influenza | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0304-8608&volume=154&issue=8&spage=1203&epage=1210&date=2009&atitle=Generation+and+evaluation+of+an+H9N1+influenza+vaccine+derived+by+reverse+genetics+that+allows+utilization+of+a+DIVA+strategy+for+control+of+H9N2+avian+influenza | - |
dc.identifier.email | Guan, Y: yguan@hkucc.hku.hk | en_HK |
dc.identifier.authority | Guan, Y=rp00397 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1007/s00705-009-0425-6 | en_HK |
dc.identifier.pmid | 19543688 | - |
dc.identifier.scopus | eid_2-s2.0-70349569546 | en_HK |
dc.identifier.hkuros | 196833 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-70349569546&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 154 | en_HK |
dc.identifier.issue | 8 | en_HK |
dc.identifier.spage | 1203 | en_HK |
dc.identifier.epage | 1210 | en_HK |
dc.identifier.isi | WOS:000269687400003 | - |
dc.publisher.place | Austria | en_HK |
dc.identifier.scopusauthorid | Wu, R=36124196300 | en_HK |
dc.identifier.scopusauthorid | Chen, Q=13008509400 | en_HK |
dc.identifier.scopusauthorid | Zheng, L=35365717800 | en_HK |
dc.identifier.scopusauthorid | Chen, J=35070971200 | en_HK |
dc.identifier.scopusauthorid | Sui, Z=26647929600 | en_HK |
dc.identifier.scopusauthorid | Guan, Y=7202924055 | en_HK |
dc.identifier.scopusauthorid | Chen, Z=13609597000 | en_HK |
dc.identifier.citeulike | 5053794 | - |
dc.identifier.issnl | 0304-8608 | - |