TY - JOUR
T1 - Improved hatchability and efficient protection after in ovo vaccination with live-attenuated H7N2 and H9N2 avian influenza viruses
AU - Cai, Yibin
AU - Song, Haichen
AU - Ye, Jianqiang
AU - Shao, Hongxia
AU - Padmanabhan, Rangarajan
AU - Sutton, Troy C.
AU - Perez, Daniel R.
N1 - Funding Information:
We are indebted to Ivan Gomez and Yonas Araya for their assistance with the animal studies. We specially thank Andrea Ferrero for her laboratory managerial skills. We thank Robert Webster and Dennis Senne for providing the highly valuable virus strains. The opinions of this manuscript are those of the authors and do not necessarily represent the views of the granting agencies. This research was made possible through funding by NIAID-NIH grant (1U01AI070469-01), CSREES-USDA grant (2005-05523, 2006-01587, 2007-04981), and NIAID-NIH contract (HHSN266200700010C) and USDA-ARS. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
PY - 2011
Y1 - 2011
N2 - Mass in ovo vaccination with live attenuated viruses is widely used in the poultry industry to protect against various infectious diseases. The worldwide outbreaks of low pathogenic and highly pathogenic avian influenza highlight the pressing need for the development of similar mass vaccination strategies against avian influenza viruses. We have previously shown that a genetically modified live attenuated avian influenza virus (LAIV) was amenable for in ovo vaccination and provided optimal protection against H5 HPAI viruses. However, in ovo vaccination against other subtypes resulted in poor hatchability and, therefore, seemed impractical. In this study, we modified the H7 and H9 hemagglutinin (HA) proteins by substituting the amino acids at the cleavage site for those found in the H6 HA subtype. We found that with this modification, a single dose in ovo vaccination of 18-day old eggs provided complete protection against homologous challenge with low pathogenic virus in 70% of chickens at 2 or 6 weeks post-hatching. Further, inoculation of 19-day old egg embryos with 10 6 EID50of LAIVs improved hatchability to 90% (equivalent to unvaccinated controls) with similar levels of protection. Our findings indicate that the strategy of modifying the HA cleavage site combined with the LAIV backbone could be used for in ovo vaccination against avian influenza. Importantly, with protection conferred as early as 2 weeks post-hatching, with this strategy birds would be protected prior to or at the time of delivery to a farm or commercial operation.
AB - Mass in ovo vaccination with live attenuated viruses is widely used in the poultry industry to protect against various infectious diseases. The worldwide outbreaks of low pathogenic and highly pathogenic avian influenza highlight the pressing need for the development of similar mass vaccination strategies against avian influenza viruses. We have previously shown that a genetically modified live attenuated avian influenza virus (LAIV) was amenable for in ovo vaccination and provided optimal protection against H5 HPAI viruses. However, in ovo vaccination against other subtypes resulted in poor hatchability and, therefore, seemed impractical. In this study, we modified the H7 and H9 hemagglutinin (HA) proteins by substituting the amino acids at the cleavage site for those found in the H6 HA subtype. We found that with this modification, a single dose in ovo vaccination of 18-day old eggs provided complete protection against homologous challenge with low pathogenic virus in 70% of chickens at 2 or 6 weeks post-hatching. Further, inoculation of 19-day old egg embryos with 10 6 EID50of LAIVs improved hatchability to 90% (equivalent to unvaccinated controls) with similar levels of protection. Our findings indicate that the strategy of modifying the HA cleavage site combined with the LAIV backbone could be used for in ovo vaccination against avian influenza. Importantly, with protection conferred as early as 2 weeks post-hatching, with this strategy birds would be protected prior to or at the time of delivery to a farm or commercial operation.
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U2 - 10.1186/1743-422X-8-31
DO - 10.1186/1743-422X-8-31
M3 - Article
C2 - 21255403
AN - SCOPUS:78651563272
SN - 1743-422X
VL - 8
JO - Virology Journal
JF - Virology Journal
M1 - 31
ER -