학술논문

Comparative Flavivirus-Host Protein Interaction Mapping Reveals Mechanisms of Dengue and Zika Virus Pathogenesis
Document Type
article
Source
Cell. 175(7)
Subject
Prevention
Infectious Diseases
Rare Diseases
Vaccine Related
Biodefense
Vector-Borne Diseases
Emerging Infectious Diseases
2.2 Factors relating to the physical environment
Aetiology
2.1 Biological and endogenous factors
Infection
Good Health and Well Being
Animals
Cell Line
Tumor
Culicidae
Dengue
Dengue Virus
HEK293 Cells
Humans
Membrane Proteins
Nuclear Proteins
Protein Interaction Mapping
Viral Nonstructural Proteins
Zika Virus
Zika Virus Infection
ANKLE2
Drosophila
PAF1C
Sec61
Zika virus
dengue virus
endoplasmic reticulum
flavivirus
interferon stimulated genes
microcephaly
proteomics
Biological Sciences
Medical and Health Sciences
Developmental Biology
Language
Abstract
Mosquito-borne flaviviruses, including dengue virus (DENV) and Zika virus (ZIKV), are a growing public health concern. Systems-level analysis of how flaviviruses hijack cellular processes through virus-host protein-protein interactions (PPIs) provides information about their replication and pathogenic mechanisms. We used affinity purification-mass spectrometry (AP-MS) to compare flavivirus-host interactions for two viruses (DENV and ZIKV) in two hosts (human and mosquito). Conserved virus-host PPIs revealed that the flavivirus NS5 protein suppresses interferon stimulated genes by inhibiting recruitment of the transcription complex PAF1C and that chemical modulation of SEC61 inhibits DENV and ZIKV replication in human and mosquito cells. Finally, we identified a ZIKV-specific interaction between NS4A and ANKLE2, a gene linked to hereditary microcephaly, and showed that ZIKV NS4A causes microcephaly in Drosophila in an ANKLE2-dependent manner. Thus, comparative flavivirus-host PPI mapping provides biological insights and, when coupled with in vivo models, can be used to unravel pathogenic mechanisms.