Revealing
the attenuating mutations of F. tularensis LVS
Recombinant
Antigen-based Assays for Flavivirus Serodiagnosis
and Surveillance
Identification
and Inhibition of Cytokines Induced During
OHFV Infection
Cell
Wall Proteins in Bacillus anthracis as
Vaccines
Rational
Design and Optimization of New Live- attenuated
Vaccines for Alphaviral
Enciphalitides
Nodavirus-based
RNA Replicon Vaccines for Tick-borne
Encephalitis Virus
Antiviral
Agents as Therapy for SARS
Typhus
Group Rickettsial Antigens Recognized by CD8+
T Lymphocytes
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Nodavirus-based
RNA Replicon Vaccines for Tick-borne Encephalitis Virus
Collaborating
Institution: University of Texas at El Paso (UTMB),
Galveston, TX
Principal
Investigator: Kyle L. Johnson, Ph.D.
Expected
Product: Vaccine for Tick-borne encephalitis viruses
Description:
Tick-borne encephalitis (TBE) viruses are important human pathogens,
particularly in Europe and Asia; one TBE virus, Powassan virus,
is endemic to North America. TBE viruses are transmitted by Ixodes
and other ticks and can cause fatal encephalitis in humans. Russian
spring-summer encephalitis virus has a 20% mortality rate, while
Central European encephalitis virus results in 1-2% mortality.
In each case, survivors are at risk for developing neurological
sequelae. An inactivated virus vaccine protects individuals exposed
to ticks in Europe but this vaccine has not been approved for
use in the United States. Despite the existence of the vaccine,
several thousand cases of TBE encephalitis are reported each
year. The National Institute for Allergy and Infectious Disease
(NIAID) Biodefense Research Agenda identifies TBE as a Category
C priority pathogen based on its transmission by an arthropod
host, its infectivity on aerosolized exposure, and its potential
threat to public health. Also, of particular concern is the possibility
that TBE viruses might be used as agents of bioterrorism. Therefore,
development of a vaccine against TBEV consistent with the overall
goals of the WRCE as well as a national biodefense priority.
The goals of this Career Development Award proposal are to develop
a candidate vaccine for tick-borne encephalitis virus and to
test its immunogenicity in mice. This proposal incorporates three
novel concepts, namely the use of Nodamura virus (NoV) RNA replicons
to amplify TBEV mRNAs in the yeast Saccharomyces cerevisiae,
the inclusion of an NoV protein that suppresses host cellular
defenses like RNA interference, and inoculation of animals with
purified total yeast RNA containing amplified NoV-TBEV RNAs.
The specific aims of this proposal are to:
1. Construct NoV RNA2-based replicons that contain TBEV structural
(glycoprotein E; M) or nonstructural (NS1) proteins and determine
the extent to which RNA replication amplifies NoV2-gpE, NoV-M and
NoV-NS1 mRNA and protein levels in yeast and mammalian cells.
2. Determine the extent to which suppression of RNA interference
by an NoV nonstructural protein enhances the efficiency of protein
expression from yeast-derived NoV RNA replicons.
3. Evaluate the TBEV structural (gpE, M) and nonstructural (NS1)
proteins as potential vaccine candidates by defining the humoral
and cell-mediated immune responses to these proteins elicited in
inoculated mice.
Relevance
to public health. Tick-borne encephalitis (TBE) viruses are
serious human pathogens that pose a threat to our public health
and our national biosafety. Our goal is to develop safe and
effective vaccine candidates that will prevent the spread of
TBE.
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