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  <controlfield tag="005">20240212023824</controlfield>
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   <subfield code="a">0010-0521015173</subfield>
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  <controlfield tag="008">240212                |          |      </controlfield>
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   <subfield code="a">en</subfield>
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   <subfield code="a">MFN/2333</subfield>
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   <subfield code="a">Risa Indriani</subfield>
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   <subfield code="a">Paul Selleck</subfield>
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   <subfield code="a">Abdul R. M. Adjid</subfield>
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   <subfield code="a">Tatty Syafriati</subfield>
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   <subfield code="a">Jagoda Ignjatovic</subfield>
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   <subfield code="a">Peter A. Durr</subfield>
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  <datafield tag="245" ind1="1" ind2=" ">
   <subfield code="a">Developing Farm-Level Post-vaccination Sero-Monitoring Systems for H5N1 Highly Pathogenic Avian InÃƒÆ’Ã‚Â¯Ãƒâ€šÃ‚Â¬ÃƒÂ¢Ã¢â€šÂ¬Ã…Â¡uenza in an Endemically Infected Country /</subfield>
   <subfield code="c">Indriani</subfield>
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  <datafield tag="260" ind1=" " ind2=" ">
   <subfield code="c">2019</subfield>
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  <datafield tag="300" ind1=" " ind2=" ">
   <subfield code="a">January 2019 | Volume 5 | Article 324</subfield>
  </datafield>
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   <subfield code="a">Whilst the serological responses of poultry following vaccination against highly pathogenic avian inÃƒÆ’Ã‚Â¯Ãƒâ€šÃ‚Â¬ÃƒÂ¢Ã¢â€šÂ¬Ã…Â¡uenza H5N1 has been extensively investigated under laboratory conditions, there have been fewer studies conducted in the ÃƒÆ’Ã‚Â¯Ãƒâ€šÃ‚Â¬Ãƒâ€šÃ‚Âeld. This applies particularly to the endemically infected countries routinely practicing vaccination, where the combination of multiple circulating clades and/or the use of vaccines with different seed strains makes the design and interpretation of ÃƒÆ’Ã‚Â¯Ãƒâ€šÃ‚Â¬Ãƒâ€šÃ‚Âeld studies especially problematic. To address this for the particular situation of layer hens in the small to medium commercial sector in Indonesia, we developed a sampling regime before and after the vaccination given to point-of-lay pullets, and assessed serological response with a panel of test antigens. This conÃƒÆ’Ã‚Â¯Ãƒâ€šÃ‚Â¬Ãƒâ€šÃ‚Ârmed that high titres were induced in those birds vaccinated with locally produced homologous H5N1 vaccines administered two or more times, but in ÃƒÆ’Ã‚Â¯Ãƒâ€šÃ‚Â¬ÃƒÂ¢Ã¢â€šÂ¬Ã…Â¡ocks using imported heterologous H5N2 vaccines median titres were signiÃƒÆ’Ã‚Â¯Ãƒâ€šÃ‚Â¬Ãƒâ€šÃ‚Âcantly lower, and unlikely to provide protection throughout the production cycle, without additional vaccination. Comparing the HI responses against the panel of antigens enabled the detection of the ÃƒÆ’Ã‚Â¯Ãƒâ€šÃ‚Â¬ÃƒÂ¢Ã¢â€šÂ¬Ã…Â¡ockÃƒÆ’Ã‚Â¢ÃƒÂ¢Ã¢â‚¬Å¡Ã‚Â¬ÃƒÂ¢Ã¢â‚¬Å¾Ã‚Â¢s exposure to different vaccine antigens, and made possible the detection of mislabelled vaccine seed strains. Furthermore, we show that test antigens need not be exactly matched to assess sero-protection in well vaccinated birds. Finally our study suggests that the POL vaccination serves as a useful reference point for following cohorts of layers throughout their production cycle, and thus enabling robust vaccination ÃƒÆ’Ã‚Â¯Ãƒâ€šÃ‚Â¬Ãƒâ€šÃ‚Âeld effectiveness studies.</subfield>
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