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J Gen Virol ; 92(Pt 9): 2181-2190, 2011 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-21632565

RESUMEN

Heterogeneous nuclear ribonucleoproteins A and B (hnRNPs A/B), cellular RNA-binding proteins that participate in splicing, trafficking, translation and turnover of mRNAs, have been implicated in the life cycles of several cytoplasmic RNA viruses. Here, we demonstrate that silencing of hnRNPs A1 and A2 significantly reduces the replication of the arenavirus Junín virus (JUNV), the aetiological agent of Argentine haemorrhagic fever. While acute JUNV infection did not modify total levels of expression of hnRNPs A/B in comparison with uninfected cells, non-cytopathic persistent infection exhibited low levels of these cell proteins. Furthermore, acutely infected cells showed a cytoplasmic relocalization of overexpressed hnRNP A1, probably related to the involvement of this protein in virus replicative cycle. This cytoplasmic accumulation was also observed in cells expressing viral nucleoprotein (N), and co-immunoprecipitation studies revealed the interaction between hnRNP A1 and N protein. By contrast, a predominantly nuclear distribution of overexpressed hnRNP A1 was found during persistent infection, even in the presence of endogenous or overexpressed N protein, indicating a differential modulation of nucleo-cytoplasmic trafficking in acute and persistent JUNV infections.


Asunto(s)
Transporte Activo de Núcleo Celular , Ribonucleoproteína Heterogénea-Nuclear Grupo A-B/metabolismo , Interacciones Huésped-Patógeno , Virus Junin/patogenicidad , ARN Viral/metabolismo , Replicación Viral , Animales , Chlorocebus aethiops , Ribonucleoproteína Nuclear Heterogénea A1 , Inmunoprecipitación , Unión Proteica , Células Vero , Proteínas Virales/metabolismo
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