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. 2011 Aug 19;8:410. doi: 10.1186/1743-422X-8-410

Figure 1.

Figure 1

Strategy for the construction of the full-length cDNA clone of an attenuated live PRRSV vaccine strain, HuN4-F112. The organization of the viral genome is shown, as are the positions of the unique restriction sites used for cloning purposes. The numbers 1a, 1b, 2a, 2b and 3 through 7 indicate the PRRSV open reading frames. An SP6 RNA promoter with two nontemplated G residues preceded the viral genome. The complete viral genome was divided into six fragments flanked by unique restriction sites, represented by the horizontal lines labeled A through F. The fragments were inserted into the modified pBluescript II SK(+) vector.