Arenavirus nucleoprotein localizes to mitochondria

Abstract

Viruses need cells to replicate and, therefore, ways to counteract the hosts immune response. Mitochondria play central roles in mediating innate immunity, hence some viruses have developed mechanisms to alter mitochondrial functions. Herein we show that arenavirus nucleoprotein (NP) enters the mitochondria of infected cells and affects their morphological integrity. We initially demonstrate electron-dense inclusions within mitochondria of reptarenavirus infected cells and hypothesized that these represent viral NP. Software predictions then serve to identify a putative N-terminal mitochondrial targeting signal (MTS) in arenavirus NPs; however, comparisons of wild-type and N-terminus mutated NPs suggest MTS-independent mitochondrial entry. NP does not enter isolated mitochondria, indicating that translocation requires additional cellular factors or conditions. Immune electron microscopy finally confirms the presence of NP within the mitochondria both in vitro and in infected animals. We hypothesize that mitochondria targeting might complement the known interferon antagonist functions of NP or alter the cells metabolic state.