Table 2.
Strain | Strategy | Target |
---|---|---|
HEP-Flury/SPBN | Deletion of the P gene | P |
SAD | Insertion of an internal ribosome entry site to control P gene transcription | P |
RC-HL/SPBN | Deletion of the M gene | M |
SPBN | Mutation of the PPEY motif | M |
SPBN/Flury-LEP/HEP-Flury | Overexpression of the G gene in the G and L gene interval | G |
SPBN | Deletion of the cytoplasmic domain of G protein | G |
ERA/SPBN/SAG | Point mutation of the G gene | G a |
HEP-Flury | Insertion of an IFN-α gene in the G and L gene interval | IFN-α |
SPBN | Insertion of an IFN-β gene in the G and L gene interval | IFN-β |
SPBN | Insertion of an IFN-γ gene in the G and L gene interval | IFN-γ |
SPBN | Insertion of a TNF-α gene in the G and L gene interval | TNF-α |
SPBN | Insertion of a cytochrome c gene in the G and L gene interval | cytochrome c |
HEP-Flury | Insertion of a MIP-1α gene in the G and L gene interval | MIP-1α |
LBNSE | Insertion of a GM-CSF gene in the G and L gene interval | GM-CSF |
LBNSE | Insertion of a Flagellin gene in the G and L gene interval | Flagellin |
ERA | Insertion of a GnRH gene in the G and L gene interval | GnRH |
TNF-α, tumor necrosis factor α; MIP-1α, macrophage inflammatory protein 1α; GnRH, gonadotropin-releasing hormone; a The point mutation of G gene strategy is always used in the form of expressing multiple copies of the mutated G gene or coupled with gene rearrangement strategy.