Gene/Protein
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Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
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Target Concepts:
Gene/Protein
Disease
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Enzyme
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Query: UNIPROT:P06889 (
Mol
)
630,302
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Novel tick-borne phleboviruses in the
Phenuiviridae
family, which are highly pathogenic in humans and all closely related to Uukuniemi virus (UUKV), have recently emerged on different continents. How phleboviruses assemble, bud, and exit cells remains largely elusive. Here, we performed high-resolution, label-free mass spectrometry analysis of UUKV immunoprecipitated from cell lysates and identified 39 cellular partners interacting with the viral envelope glycoproteins. The importance of these host factors for UUKV infection was validated by silencing each host factor by RNA interference. This revealed
Golgi-specific brefeldin A-resistance guanine nucleotide exchange factor 1
(
GBF1
), a guanine nucleotide exchange factor resident in the Golgi, as a critical host factor required for the UUKV life cycle. An inhibitor of
GBF1
, Golgicide A, confirmed the role of the cellular factor in UUKV infection. We could pinpoint the
GBF1
requirement to UUKV replication and particle assembly. When the investigation was extended to viruses from various positive and negative RNA viral families, we found that not only phleboviruses rely on
GBF1
for infection, but also
Flavi
-,
Corona
-,
Rhabdo
-, and
Togaviridae
In contrast, silencing or blocking
GBF1
did not abrogate infection by the human adenovirus serotype 5 and immunodeficiency retrovirus type 1, the replication of both requires nuclear steps. Together our results indicate that UUKV relies on
GBF1
for viral replication, assembly and egress. This study also highlights the proviral activity of
GBF1
in the infection by a broad range of important zoonotic RNA viruses.
Mol
Cell Proteomics 2019 12
PMID:Quantitative Proteomics of Uukuniemi Virus-host Cell Interactions Reveals GBF1 as Proviral Host Factor for Phleboviruses. 3157 Apr 97