scholarly journals Role of Communally Nesting Ardeid Birds in the Epidemiology of West Nile Virus Revisited

2009 ◽  
Vol 9 (3) ◽  
pp. 275-280 ◽  
Author(s):  
William K. Reisen ◽  
Sarah Wheeler ◽  
M. Veronica Armijos ◽  
Ying Fang ◽  
Sandra Garcia ◽  
...  
Keyword(s):  
West Nile Virus ◽  
West Nile ◽  
Communally Nesting

scholarly journals Potential Dual Role of West Nile Virus NS2B in Orchestrating NS3 Enzymatic Activity in Viral Replication

Viruses ◽  
2021 ◽  
Vol 13 (2) ◽  
pp. 216
Author(s):  
Alanna C. Tseng ◽  
Vivek R. Nerurkar ◽  
Kabi R. Neupane ◽  
Helmut Kae ◽  
Pakieli H. Kaufusi
Keyword(s):  
West Nile Virus ◽  
Enzymatic Activity ◽  
Nonstructural Protein ◽  
Antiviral Drug ◽  
West Nile ◽  
Biochemical Assays ◽  
In Trans ◽  
Viral Polyprotein ◽  
Ns3 Protease

West Nile virus (WNV) nonstructural protein 3 (NS3) harbors the viral triphosphatase and helicase for viral RNA synthesis and, together with NS2B, constitutes the protease responsible for polyprotein processing. NS3 is a soluble protein, but it is localized to specialized compartments at the rough endoplasmic reticulum (RER), where its enzymatic functions are essential for virus replication. However, the mechanistic details behind the recruitment of NS3 from the cytoplasm to the RER have not yet been fully elucidated. In this study, we employed immunofluorescence and biochemical assays to demonstrate that NS3, when expressed individually and when cleaved from the viral polyprotein, is localized exclusively to the cytoplasm. Furthermore, NS3 appeared to be peripherally recruited to the RER and proteolytically active when NS2B was provided in trans. Thus, we provide evidence for a potential additional role for NS2B in not only serving as the cofactor for the NS3 protease, but also in recruiting NS3 from the cytoplasm to the RER for proper enzymatic activity. Results from our study suggest that targeting the interaction between NS2B and NS3 in disrupting the NS3 ER localization may be an attractive avenue for antiviral drug discovery.

scholarly journals An interaction between the methyltransferase and RNA dependent RNA polymerase domains of the West Nile virus NS5 protein

2013 ◽  
Vol 94 (9) ◽  
pp. 1961-1971 ◽  
Author(s):  
Cindy S. E. Tan ◽  
Jody M. Hobson-Peters ◽  
Martin J. Stoermer ◽  
David P. Fairlie ◽  
Alexander A. Khromykh ◽  
...  
Keyword(s):  
West Nile Virus ◽  
Rna Polymerase ◽  
Genetic Interaction ◽  
Nonstructural Protein ◽  
Specific Interaction ◽  
Simian Virus 40 ◽  
T Antigen ◽  
Rna Dependent Rna Polymerase ◽  
West Nile

The flavivirus nonstructural protein 5 (NS5) is a large protein that is structurally conserved among members of the genus, making it an attractive target for antiviral drug development. The protein contains a methyltransferase (MTase) domain and an RNA dependent RNA polymerase (POL) domain. Previous studies with dengue viruses have identified a genetic interaction between residues 46–49 in the αA3-motif in the MTase and residue 512 in POL. These genetic interactions are consistent with structural modelling of these domains in West Nile virus (WNV) NS5 that predict close proximity of these regions of the two domains, and potentially a functional interaction mediated via the αA3-motif. To demonstrate an interaction between the MTase and POL domains of the WNV NS5 protein, we co-expressed affinity-tagged recombinant MTase and POL proteins in human embryonic kidney cells with simian virus 40 large T antigen (HEK293T cells) and performed pulldown assays using an antibody to the flag tag on POL. Western blot analysis with an anti-MTase mAb revealed that the MTase protein was specifically co-immunoprecipitated with POL, providing the first evidence of a specific interaction between these domains. To further assess the role of the αA3 helix in this interaction, selected residues in this motif were mutated in the recombinant MTase and the effect on POL interaction determined by the pulldown assay. These mutations were also introduced into a WNV infectious clone (FLSDX) and the replication properties of these mutant viruses assessed. While none of the αA3 mutations had a significant effect on the MTase–POL association in pulldown assays, suggesting that these residues were not specific to the interaction, an E46L mutation completely abolished virus viability indicating a critical requirement of this residue in replication. Failure to generate compensatory mutations in POL to rescue replication, even after several passages of the transfection supernatant in Vero cells, precluded further conclusion of the role of this residue in the context of MTase–POL interactions.

WEST NILE VIRUS INFECTION OF PRIMARY MOUSE NEURONAL AND NEUROGLIAL CELLS: THE ROLE OF ASTROCYTES IN CHRONIC INFECTION

2006 ◽  
Vol 75 (4) ◽  
pp. 691-696 ◽  
Author(s):  
JOSE A. P. DINIZ ◽  
HILDA GUZMAN ◽  
VSEVOLOD L. POPOV ◽  
PEDRO F. C. VASCONCELOS ◽  
FANGLING XU ◽  
...  
Keyword(s):  
West Nile Virus ◽  
Virus Infection ◽  
Chronic Infection ◽  
West Nile Virus Infection ◽  
West Nile ◽  
Primary Mouse

scholarly journals Role of enhanced vector transmission of a new West Nile virus strain in an outbreak of equine disease in Australia in 2011

2014 ◽  
Vol 7 (1) ◽  
Author(s):  
Andrew F van den Hurk ◽  
Sonja Hall-Mendelin ◽  
Cameron E Webb ◽  
Cindy S E Tan ◽  
Francesca D Frentiu ◽  
...  
Keyword(s):  
West Nile Virus ◽  
Virus Strain ◽  
West Nile ◽  
Vector Transmission ◽  
New West ◽  
West Nile Virus Strain

scholarly journals The Role of Innate Immunity in Conditioning Mosquito Susceptibility to West Nile Virus

Viruses ◽  
2013 ◽  
Vol 5 (12) ◽  
pp. 3142-3170 ◽  
Author(s):  
Abhishek Prasad ◽  
Doug. Brackney ◽  
Gregory Ebel
Keyword(s):  
Innate Immunity ◽  
West Nile Virus ◽  
West Nile
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