Protection of non-murine mammals against encephalomyocarditis virus using a genetically engineered Mengo virus
Abstract
Genetically engineered Mengo viruses with artificial deletions in the 5' noncoding poly(C) tracts are highly attenuated for pathogenicity when introduced as live vaccines into the natural murine host. Inoculation produces lifelong protective immunity without disease or viral persistence. This report extends the vaccination studies to non-murine hosts, including baboons, macaques and domestic pigs, all of which are susceptible to severe cardiovirus epizootics. All animals of these species that were inoculated with vMC24, an engineered strain of Mengo, seroconverted. When the immunized animals were challenged, they were protected against lethal doses of encephalomyocarditis virus (EMCV) derived from currently circulating epizootic strains. In baboons, the neutralizing antibody titers induced by vMC24 were significantly higher than from an inactivated EMCV vaccine. Moreover, terminal histopathology on baboons (inoculated intramuscularly), macaques (inoculated intracerebrally), and pigs (inoculated intramuscularly) showed few, if any, gross lesions characteristic of EMCV-like disease, in the vMC24 vaccinates. We suggest that genetically engineered, short poly(C) Mengo viruses may be universally potent attenuated vaccines for many types of animals and can possibly provide safe, efficacious protection against all cardioviruses of the EMCV serotype.
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Killed autogenous vaccines can induce long-lived, and in some cases, high-titer neutralizing antibodies that are likely protective against EMCV-related disease in elephants.
“These results suggest that killed autogenous vaccines – which in most circumstances are the only current option available to zoos for protecting their animals – can nevertheless induce long-lived, and in some cases, high-titer neutralizing antibodies that are likely protective against EMCV-related disease in elephants.”
From Zoological transmission of encephalomyocarditis virus in the United States: Virus evolution, host ecology, and capsid antigenicity derived from an outbreak (2026) · cites this paper as [76]
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“However, it has been demonstrated that titers ≥1:20 are protective in mice after challenge [76], and in one study, inactivated vaccine-induced antibodies were protective in African elephants subsequently challenged with EMCV [32].”
- Authors
- Osorio, J. E., Hubbard, G. B., Soike, K. F., Girard, M., van der Werf, S., Moulin, J.-C., & Palmenberg, A. C.
- Affiliations
- University of Wisconsin–Madison (US)
- Texas Biomedical Research Institute (US)
- Tulane University (US)
- Institut Pasteur (FR)
- Corresponding author
- Palmenberg, Ann C.
- Venue
- Vaccine
- Publisher
- Elsevier BV
- Published
- 1996-02
- Volume
- 14
- Issue
- 2
- Pages
- 155-161
- ISSN
- 0264-410X (ISSN-L)
- OpenAlex
- W2013698424
- Cited by
- 41
- References
- 23
- Citations by year
- 2026: 2 · 2025: 4 · 2024: 1 · 2023: 1 · 2022: 1 · 2021: 2 · 2017: 1 · 2016: 3 · 2014: 1 · 2012: 2
- FWCI
- 5.04
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Vaccine (publishedVersion)
- PubMed (publishedVersion)
- Funders
- University of Wisconsin-Madison
- National Institutes of Health (5r01ai030566-09)
- National Institute of Allergy and Infectious Diseases (AI-30566)
- National Center for Research Resources (P51RR000164, RR00164.)
- Topics
- Life Sciences › Agricultural and Biological Sciences › Animal Science and Zoology › Animal Virus Infections Studies
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Viral Infections and Immunology Research
- Health Sciences › Medicine › Epidemiology › Virology and Viral Diseases
- Keywords
- encephalomyocarditis virus, mengovirus, live attenuated vaccine, 5' untranslated region, baboons, macaque, pigs, neutralizing antibodies, seroconversion, vaccine safety
- MeSH terms
- Animals, Encephalomyocarditis virus, Female, Genetic Engineering, HeLa Cells, Humans, Macaca mulatta, Mengovirus, Papio, Poly C, Swine, Viral Vaccines, Cardiovirus Infections
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