Mutations that positively affect Bandavirus glycoprotein function in VSV-vectored vaccines
- 1Department of Microbiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA
- 2Department of Animal, Dairy, and Veterinary Sciences, Utah State University, Logan, Utah, USA
Abstract
Severe fever with thrombocytopenia syndrome virus (SFTSV) and Heartland bandavirus (HRTV) are emerging tick-borne bandaviruses. They have high case fatality rates (10%), and no FDA-approved vaccines exist for disease prevention. SFTSV and HRTV are therefore identified as priority pathogens. A recombinant vesicular stomatitis virus (rVSV) vaccine, which replaces the original VSV glycoprotein with the SFTSV glycoproteins, shows early promise for SFTSV as it induces strong immune responses that are protective against lethal challenge. However, rVSV-SFTSV is highly attenuated in cell culture, which may be due to incompatibility between the assembly sites of SFTSV (the Golgi and endoplasmic reticulum-Golgi intermediate compartment [ERGIC]) and those of VSV (the plasma membrane). In this study, we identify a noncanonical coatomer complex I (COPI)-binding motif found in the cytoplasmic tail of SFTSV glycoproteins and demonstrate that an amino acid substitution in this motif (K1071A) inhibits binding to COPI. This mutation results in increased surface expression of SFTSV glycoproteins, improved incorporation onto VSV virions, and enhanced replication of rVSV-SFTSV in vitro. A mutation at a homologous site (K1074A) in HRTV yields similar results, and rVSV-HRTV K1074A exhibits increased replication in vitro and in vivo. We show that vaccination with rVSV-HRTV K1074A results in improved induction of neutralizing antibody responses in immunocompetent C57BL/6 mice, and neutralizing antibodies elicited by vaccination are protective when administered to severely immunocompromised mice via passive transfer. Overall, our study identifies a mutation that improves the efficacy of the rVSV-SFTSV vaccine candidate and introduces the first vaccine candidate directly addressing HRTV infections.
IMPORTANCE: Severe fever with thrombocytopenia syndrome virus (SFTSV) and Heartland bandavirus (HRTV) are emerging tick-borne viruses with high fatality rates. FDA-approved vaccines and antiviral drugs are unavailable but critically needed. We identify an important mutation in the SFTSV glycoprotein that disrupts a previously unreported COPI-binding site. The mutation improves the efficacy of the previously described recombinant vesicular stomatitis virus vaccine candidate for SFTSV (rVSV-SFTSV). We also develop an rVSV-HRTV vaccine and show potent induction of neutralizing antibodies and protection from lethal challenge. This is the first study directly addressing the lack of vaccines specifically targeting HRTV.
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BibTeX
@article{petch2026mutations,
title = {{Mutations that positively affect Bandavirus glycoprotein function in VSV-vectored vaccines}},
author = {Raegan J. Petch and Philip Hicks and Jonna B. Westover and Brian B. Gowen and Paul Bates},
journal = {Journal of Virology},
year = {2026},
month = sep,
doi = {10.1128/jvi.01311-26},
url = {https://doi.org/10.1128/jvi.01311-26},
note = {CC BY 4.0},
}
RIS
TY - JOUR
TI - Mutations that positively affect Bandavirus glycoprotein function in VSV-vectored vaccines
AU - Raegan J. Petch
AU - Philip Hicks
AU - Jonna B. Westover
AU - Brian B. Gowen
AU - Paul Bates
PY - 2026
DA - 2026/09/24
JO - Journal of Virology
DO - 10.1128/jvi.01311-26
UR - https://doi.org/10.1128/jvi.01311-26
AB - Severe fever with thrombocytopenia syndrome virus (SFTSV) and Heartland bandavirus (HRTV) are emerging tick-borne bandaviruses. They have high case fatality rates (10%), and no FDA-approved vaccines exist for disease prevention. SFTSV and HRTV are therefore identified as priority pathogens. A recombinant vesicular stomatitis virus (rVSV) vaccine, which replaces the original VSV glycoprotein with the SFTSV glycoproteins, shows early promise for SFTSV as it induces strong immune responses that are protective against lethal challenge. However, rVSV-SFTSV is highly attenuated in cell culture, which may be due to incompatibility between the assembly sites of SFTSV (the Golgi and endoplasmic reticulum-Golgi intermediate compartment [ERGIC]) and those of VSV (the plasma membrane). In this study, we identify a noncanonical coatomer complex I (COPI)-binding motif found in the cytoplasmic tail of SFTSV glycoproteins and demonstrate that an amino acid substitution in this motif (K1071A) inhibits binding to COPI. This mutation results in increased surface expression of SFTSV glycoproteins, improved incorporation onto VSV virions, and enhanced replication of rVSV-SFTSV in vitro. A mutation at a homologous site (K1074A) in HRTV yields similar results, and rVSV-HRTV K1074A exhibits increased replication in vitro and in vivo. We show that vaccination with rVSV-HRTV K1074A results in improved induction of neutralizing antibody responses in immunocompetent C57BL/6 mice, and neutralizing antibodies elicited by vaccination are protective when administered to severely immunocompromised mice via passive transfer. Overall, our study identifies a mutation that improves the efficacy of the rVSV-SFTSV vaccine candidate and introduces the first vaccine candidate directly addressing HRTV infections. IMPORTANCE: Severe fever with thrombocytopenia syndrome virus (SFTSV) and Heartland bandavirus (HRTV) are emerging tick-borne viruses with high fatality rates. FDA-approved vaccines and antiviral drugs are unavailable but critically needed. We identify an important mutation in the SFTSV glycoprotein that disrupts a previously unreported COPI-binding site. The mutation improves the efficacy of the previously described recombinant vesicular stomatitis virus vaccine candidate for SFTSV (rVSV-SFTSV). We also develop an rVSV-HRTV vaccine and show potent induction of neutralizing antibodies and protection from lethal challenge. This is the first study directly addressing the lack of vaccines specifically targeting HRTV.
SN - 0022-538X
SN - 1098-5514
ER -