Misinzo, G.Delputte, P. L.Lefebvre, D. J.Nauwynck, H. J.2017-06-232017-06-232007-12-17https://www.suaire.sua.ac.tz/handle/123456789/1671Archives virology 2008, Vol. 153: 337–342Treatment of porcine kidney (PK-15) cells with either interferon-gamma (IFN-g) or endosomallysosomal system acidification inhibitors increases replication of porcine circovirus type 2 (PCV2). In the present study, the effect of a combination of these treatments on the number of infected cells and virus yield was tested. The number of PCV2 (Stoon-1010)-infected PK-15 cells increased in cells treated with ammonium chloride (445 39% increase), IFN-g (446 8%), ammonium chlorideþ IFN-g (1721 283%), chloroquine diphosphate (1037 121%), chloroquine diphosphateþIFN-g (2199 255%), monensin (950 178%) and monensinþIFN-g (1948 60%). Combined IFNg and endosomal-lysosomal system acidification inhibitors increased PCV2 yield by up to 50 times compared to untreated PK-15. This augmented virus replication in PK-15 cells may be helpful in the production of PCV2 vaccines.enPorcine circovirus-2PK-15 cellsEndosomallysosomal systemInterferon-gamma (IFN-g)Article