analysis of subcellular prefoldin 1 redistribution during rabies virus infection

conclusions the results of this work demonstrated that the subcellular distribution of pfdn1 was altered in the rabv-infected n2a cells and colocalized with the n protein of rabv in the nbl structures. results confocal microscopy showed that pfdn1 was colocalized with the n protein of rabv in the infected n2a cells and was mainly recruited to the characteristic negri-body-like (nbl) structures in the cytoplasm, as well as the cotransfection of the n and p genes of rabv. the transcription of pfdn1 in the rabv-infected n2a cells was upregulated, whereas the transfection of the n and/or p genes did not result in the upregulation of pfdn1. materials and methods mouse neuro-2a (n2a) cells were infected by rabv or transfected with the plasmids of the nucleoprotein (n) and/or phosphoprotein (p) gene of rabv. the subcellular distribution of pfdn1 was analyzed by confocal microscopy, and the transcription levels of pfdn1 in the n and/or p gene of the rabv-transfected or rabv-infected n2a cells were assessed via real-time quantitative polymerase chain reaction. objectives this study aimed to investigate the change in the subcellular distribution and expression of the host protein prefoldin subunit 1 (pfdn1) in rabv-infected cells and the viral expression of plasmids in the transfected cells. background rabies virus (rabv) is one of the old deadly zoonotic viruses. it attacks the central nervous system and causes acute encephalitis in humans and animals. host factors are known to be essential for virus infection and replication in cells. the identification of the key host factors required for rabv infection may provide important information on rabv replication and may provide new potential targets for rabv drug discovery.