| Literature DB >> 28919920 |
Jaclyn A Kaiser1,1, Tian Wang1,2,3,1,2,3, Alan Dt Barrett1,2,3,1,2,3.
Abstract
West Nile virus (WNV), a neurotropic mosquito-borne flavivirus, has become endemic in the USA and parts of Europe since 1999. There is no licensed WNV vaccine for humans. Considering the robust immunity from immunization with live, attenuated vaccines, a live WNV vaccine is an ideal platform for disease control. Animal and mosquito studies have identified a number of candidate attenuating mutations, including the structural proteins premembrane/membrane and envelope, and the nonstructural proteins NS1, NS2A, NS3, NS4A, NS4B and NS5, and the 3' UTR. Many of the mutations that have been examined attenuate WNV using different mechanisms, thus providing a greater understanding of WNV virulence while also identifying specific mutations as candidates to include in a WNV live vaccine.Entities:
Keywords: West Nile virus; attenuation; flavivirus; live attenuated vaccine; virulence
Year: 2017 PMID: 28919920 PMCID: PMC5592643 DOI: 10.2217/fvl-2016-0141
Source DB: PubMed Journal: Future Virol ISSN: 1746-0794 Impact factor: 1.831