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Development of a Broadly Accessible Venezuelan Equine Encephalitis Virus Replicon Particle Vaccine Platform.
Agnihothram, Sudhakar; Menachery, Vineet D; Yount, Boyd L; Lindesmith, Lisa C; Scobey, Trevor; Whitmore, Alan; Schäfer, Alexandra; Heise, Mark T; Baric, Ralph S.
Affiliation
  • Agnihothram S; Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
  • Menachery VD; Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
  • Yount BL; Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, Texas, USA.
  • Lindesmith LC; Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
  • Scobey T; Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
  • Whitmore A; Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
  • Schäfer A; Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
  • Heise MT; Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
  • Baric RS; Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
J Virol ; 92(11)2018 06 01.
Article in En | MEDLINE | ID: mdl-29540599
Zoonotic viruses circulate as swarms in animal reservoirs and can emerge into human populations, causing epidemics that adversely affect public health. Portable, safe, and effective vaccine platforms are needed in the context of these outbreak and emergence situations. In this work, we report the generation and characterization of an alphavirus replicon vaccine platform based on a non-select agent, attenuated Venezuelan equine encephalitis (VEE) virus vaccine, strain 3526 (VRP 3526). Using both noroviruses and coronaviruses as model systems, we demonstrate the utility of the VRP 3526 platform in the generation of recombinant proteins, production of virus-like particles, and in vivo efficacy as a vaccine against emergent viruses. Importantly, packaging under biosafety level 2 (BSL2) conditions distinguishes VRP 3526 from previously reported alphavirus platforms and makes this approach accessible to the majority of laboratories around the world. In addition, improved outcomes in the vulnerable aged models as well as against heterologous challenge suggest improved efficacy compared to that of previously attenuated VRP approaches. Taking these results together, the VRP 3526 platform represents a safe and highly portable system that can be rapidly deployed under BSL2 conditions for generation of candidate vaccines against emerging microbial pathogens.IMPORTANCE While VEE virus replicon particles provide a robust, established platform for antigen expression and vaccination, its utility has been limited by the requirement for high-containment-level facilities for production and packaging. In this work, we utilize an attenuated vaccine strain capable of use at lower biocontainment level but retaining the capacity of the wild-type replicon particle. Importantly, the new replicon platform provides equal protection for aged mice and following heterologous challenge, which distinguishes it from other attenuated replicon platforms. Together, the new system represents a highly portable, safe system for use in the context of disease emergence.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Vaccines, Attenuated / Viral Vaccines / Severe Acute Respiratory Syndrome / Severe acute respiratory syndrome-related coronavirus / Encephalitis Virus, Venezuelan Equine / Encephalomyelitis, Venezuelan Equine / Antibodies, Viral Limits: Animals / Female / Humans Country/Region as subject: America do sul / Venezuela Language: En Journal: J Virol Year: 2018 Document type: Article Affiliation country: United States Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Vaccines, Attenuated / Viral Vaccines / Severe Acute Respiratory Syndrome / Severe acute respiratory syndrome-related coronavirus / Encephalitis Virus, Venezuelan Equine / Encephalomyelitis, Venezuelan Equine / Antibodies, Viral Limits: Animals / Female / Humans Country/Region as subject: America do sul / Venezuela Language: En Journal: J Virol Year: 2018 Document type: Article Affiliation country: United States Country of publication: United States