Alphavirus
for
Biodefense
Recombinant Genetics
Development
for
Junin Viruses
Improving
Small Animal Models of Chikungunya Fever for Development of
New Live-Attenuated vaccines
Nipah
Virus-like Particles for Vaccine Development
Defining
Protective Human T-cell Epitopes in Rift Valley Fever Virus
NSs
Function of Rift Valley
Fever Virus MP-12 Vaccine Strain
Structural
and Biochemical Characterization of Japanese Encephalitis
Virus Vaccine Candidates
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WRCE
Theme 2: Vaccine Development for Arboviral and Emerging Viral Diseases
Theme
Leader: Scott Weaver, PhD – University of Texas
Medical Branch, Galveston, TX
Expected
Product: The proposed projects in Theme 2 will develop
improved vaccine technologies to both protect the US population
against these emerging viral diseases, and mitigate endemic transmission
in tropical locations that increases our risk of importation.
Description: The
continued emergence of highly pathogenic RNA viruses represents
a severe
threat to human health. Among the most
important emerging pathogens are the arthropod-borne viruses (arboviruses)
that comprise a taxonomically diverse group of agents that share
vector-borne transmission. Nearly all arboviruses that cause human
disease belong to three families: (1) the genus Flavivirus in the
family Flaviviridae; (2) the genus Alphavirus in the family Togaviridae;
and (3) several genera in the family Bunyaviridae. Most of these
viruses are zoonotic and utilize mosquitoes or ticks for transmission
among wild animals. Humans usually become infected when amplification
in the zoonotic cycle leads to “spillover.” Arboviral
infections are therefore particularly difficult to prevent because
the wild animal reservoir hosts and enzootic arthropod vectors
cannot be controlled in an environmentally acceptable manner. Reemerging
viral diseases, including Argentine hemorrhagic fever, and emerging
viral disease such as Nipah virus infection, are also of major
public health importance. The activities of this theme are devoted
to developing live attenuated vaccines and improved animal models
for alphaviruses, building upon our expertise in arboviral genetics;
determining the mechanism of attenuation for MP-12, the vaccine
strain for Rift Valley fever virus; developing a reverse genetics
system for Junin virus; and producing Nipah virus-like particles
for use as protective immunogens.
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