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Protection by Recombinant Newcastle Disease Viruses (NDV) Expressing the Glycoprotein (G) of Avian Metapneumovirus (aMPV) Subtype A or B against Challenge with Virulent NDV and aMPV

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Figure 1. Schematic representation of pLS/aMPV-AG and -BG construction. The open reading frame of the G gene of aMPV-A or -B, amplified from virus genomic RNA, was cloned into the intergenic region between the F and HN genes in the pFLC-LaSota vector throu
Figure 2. Cytopathic effects induced by the recombinant viruses. Monolayers of DF-1 cells were infected with rLS/aMPV-A G, rLS/aMPV-B G, or LaSota virus at an MOI of 0.001
Figure 3. Growth dynamics of the recombinant viruses. DF-1 cells were infected with rLS/aMPV-A G, rLS/aMPV-B G or LaSota strain at an MOI of 0.01
Table 3. Serum antibody response of turkeys against NDV following vaccination and survival of turkeys after challenge with a lethal dose of NDV/CA02
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