PLA2G16 represents a switch between entry and clearance of Picornaviridae.
Nature
; 541(7637): 412-416, 2017 01 19.
Article
em En
| MEDLINE
| ID: mdl-28077878
ABSTRACT
Picornaviruses are a leading cause of human and veterinary infections that result in various diseases, including polio and the common cold. As archetypical non-enveloped viruses, their biology has been extensively studied. Although a range of different cell-surface receptors are bound by different picornaviruses, it is unclear whether common host factors are needed for them to reach the cytoplasm. Using genome-wide haploid genetic screens, here we identify the lipid-modifying enzyme PLA2G16 (refs 8, 9, 10, 11) as a picornavirus host factor that is required for a previously unknown event in the viral life cycle. We find that PLA2G16 functions early during infection, enabling virion-mediated genome delivery into the cytoplasm, but not in any virion-assigned step, such as cell binding, endosomal trafficking or pore formation. To resolve this paradox, we screened for suppressors of the ΔPLA2G16 phenotype and identified a mechanism previously implicated in the clearance of intracellular bacteria. The sensor of this mechanism, galectin-8 (encoded by LGALS8), detects permeated endosomes and marks them for autophagic degradation, whereas PLA2G16 facilitates viral genome translocation and prevents clearance. This study uncovers two competing processes triggered by virus entry activation of a pore-activated clearance pathway and recruitment of a phospholipase to enable genome release.
Texto completo:
1
Base de dados:
MEDLINE
Assunto principal:
Picornaviridae
/
Genoma Viral
/
Citoplasma
/
Proteínas Supressoras de Tumor
/
Internalização do Vírus
/
Fosfolipases A2 Independentes de Cálcio
/
Fatores Celulares Derivados do Hospedeiro
Idioma:
En
Ano de publicação:
2017
Tipo de documento:
Article