Influenza A Virus Induces Autophagosomal Targeting of Ribosomal Proteins

Autor: Jörn Dengjel, Verónica I. Dumit, Lea Bühler, Carole Roubaty, Martin Schwemmle, Shadi Abou-Eid, Christine Gretzmeier, Monique Gannagé, Zehan Hu, Stéphanie Kaeser-Pebernard, Andrea C. Becker, Christian Münz, Sebastian Giese, Petra Paul
Přispěvatelé: University of Zurich, Dengjel, Jörn
Jazyk: angličtina
Rok vydání: 2018
Předmět:
0301 basic medicine
1303 Biochemistry
Proteome
organelle
Cell
autophagosome
medicine.disease_cause
Proteomics
10263 Institute of Experimental Immunology
SILAC
Autophagosomes/*metabolism
Autophagy
Cell Line
Tumor

Humans
Influenza A virus/*metabolism
Influenza
Human/metabolism/pathology/virology

Proteome/metabolism
RNA
Messenger/genetics/metabolism

RNA
Viral/metabolism

Ribosomal Proteins/*metabolism
Ribosomes/metabolism
Cell biology
Ribosomes
silac
Viruses
cell line
proteomics
vesicle
Biochemistry
Analytical Chemistry
0302 clinical medicine
Interferon
Influenza A virus
1602 Analytical Chemistry
3. Good health
medicine.anatomical_structure
RNA
Viral

medicine.drug
Ribosomal Proteins
Viral protein
610 Medicine & health
Biology
Virus
03 medical and health sciences
Ribosomal protein
Influenza
Human

medicine
1312 Molecular Biology
RNA
Messenger

Molecular Biology
Research
Autophagosomes
Virology
030104 developmental biology
Cell culture
570 Life sciences
biology
030217 neurology & neurosurgery
Zdroj: Mol Cell Proteomics, vol. 17, no. 10, pp. 1909-1921
Molecular & Cellular Proteomics : MCP
Popis: Seasonal epidemics of influenza A virus are a major cause of severe illness and are of high socio-economic relevance. For the design of effective antiviral therapies, a detailed knowledge of pathways perturbed by virus infection is critical. We performed comprehensive expression and organellar proteomics experiments to study the cellular consequences of influenza A virus infection using three human epithelial cell lines derived from human lung carcinomas: A549, Calu-1 and NCI-H1299. As a common response, the type I interferon pathway was up-regulated upon infection. Interestingly, influenza A virus infection led to numerous cell line-specific responses affecting both protein abundance as well as subcellular localization. In A549 cells, the vesicular compartment appeared expanded after virus infection. The composition of autophagsomes was altered by targeting of ribosomes, viral mRNA and proteins to these double membrane vesicles. Thus, autophagy may support viral protein translation by promoting the clustering of the respective molecular machinery in autophagosomes in a cell line-dependent manner.
Databáze: OpenAIRE