The infectious titers showed a clear trend: icPC22A exhibited the highest titer, followed by dORF3-EGFP and RMTv1, which had comparable titers, while all three double IFN antagonist mutants (RMTv1-nsp1 + nsp15, RMTv1-nsp1 + nsp16, and RMTv1-nsp15 + nsp16) displayed significantly reduced titers.
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Engineering a recombination-resistant live attenuated vaccine candidate with suppressed interferon antagonists for PEDV.
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