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Stability of viability and immunizing potency of lyophilized, modified equine arteritis live-virus vaccine.

Abstract: The Bucyrus strain of equine arteritis virus, previously modified to avirulence and vaccinal virus by 131 serial passages in primary cell cultures of horse kidney followed by 111 passages in primary cell cultures of rabbit kidney, was further passaged in cultures of the E. Derm (NBL-6) cell line, a continuous diploid cell line. Pools of the 16th and 25th passages of the virus in this last equine dermal cell line were lyophilized and stored in lots at 37 C, 23 to 28 C, 4C, and -20 C. The viability of the vaccinal virus deteriorated rapidly during storage at 37 C and at 23 to 28 C, but was relatively stable at 4 C and at -20 C for at least 1 year. The vaccine stored at 4 C for 9 months protected 2 horses, subsequently inoculated with avirulent virus, from arteritis, whereas the 2 nonvaccinated control horses inoculated simultaneously developed severe signs of the disease and died of acute arteritis.
Publication Date: 1981-09-01 PubMed ID: 6275755
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  • Comparative Study
  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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This research investigates the stability and immunizing potency of a specially modified live-virus vaccine for equine arteritis. The findings suggest that when stored at colder temperatures, the vaccine retains its viability and ability to protect against the disease for a longer period.

Background of the Research

  • The vaccine in this study is made from the Bucyrus strain of equine arteritis virus. It was modified into a non-threatening, vaccinal virus through 131 serial passages in primary cell cultures of horse kidney, and then 111 passages in primary cell cultures of rabbit kidney. A passage is a round of growing the virus in cell cultures and then transferring it to a new set of fresh cells – a process that often modifies the virus into a form that is no longer harmful.
  • For this research, the researchers further passaged the virus in cultures of the E. Derm (NBL-6) cell line. This is a continuous diploid cell line – a line of cells that divide and reproduce indefinitely and retain the exact same genetic material.

Stability of the Vaccine

  • Following the additional passages in the E. Derm (NBL-6) cell line, vaccines from the 16th and 25th passages were lyophilized – a method for freeze-drying. This makes the vaccine easier to store and transport.
  • The dry vaccines were then stored at different temperatures: 37 C, 23 to 28 C, 4 C, and -20 C. The goal was to see how well the vaccine survived in different conditions over time.
  • Results revealed that the vaccine’s viability deteriorated rapidly at higher temperatures (37 C and 23 to 28 C). However, when stored at colder temperatures (4 C and -20 C), it remained relatively stable for at least 1 year.

Efficacy of the Vaccine

  • The researchers also tested the vaccine on horses to ensure it was still effective after storage. The vaccine stored at 4 C for 9 months was used to inoculate 2 horses, while two other non-vaccinated horses served as controls.
  • The vaccinated horses were then exposed to the avirulent virus of equine arteritis. The two vaccinated horses were protected from the disease. However, the control horses developed severe symptoms of arteritis and died from acute arteritis.
  • This result indicates that the vaccine, when stored properly at low temperatures, not only retains its viability but also continues to provide a strong immune response against equine arteritis.

Cite This Article

APA
Harry TO, McCollum WH. (1981). Stability of viability and immunizing potency of lyophilized, modified equine arteritis live-virus vaccine. Am J Vet Res, 42(9), 1501-1505.

Publication

ISSN: 0002-9645
NlmUniqueID: 0375011
Country: United States
Language: English
Volume: 42
Issue: 9
Pages: 1501-1505

Researcher Affiliations

Harry, T O
    McCollum, W H

      MeSH Terms

      • Animals
      • Antibodies, Viral / analysis
      • Cell Line
      • Equartevirus / growth & development
      • Equartevirus / immunology
      • Equartevirus / isolation & purification
      • Freeze Drying
      • Horse Diseases / microbiology
      • Horse Diseases / prevention & control
      • Horses
      • RNA Viruses / growth & development
      • Temperature
      • Time Factors
      • Viral Plaque Assay
      • Viral Vaccines / immunology
      • Virulence
      • Virus Diseases / microbiology
      • Virus Diseases / prevention & control
      • Virus Diseases / veterinary

      Citations

      This article has been cited 7 times.
      1. Thieulent CJ, Sarkar S, Carossino M, Bhowmik M, Zhu H, Balasuriya UBR. Cell Surface Vimentin Is an Attachment Factor That Facilitates Equine Arteritis Virus Infection In Vitro. Viruses 2026 Jan 15;18(1).
        doi: 10.3390/v18010113pubmed: 41600875google scholar: lookup
      2. Balasuriya UB, Zhang J, Go YY, MacLachlan NJ. Experiences with infectious cDNA clones of equine arteritis virus: lessons learned and insights gained. Virology 2014 Aug;462-463:388-403.
        doi: 10.1016/j.virol.2014.04.029pubmed: 24913633google scholar: lookup
      3. Go YY, Zhang J, Timoney PJ, Cook RF, Horohov DW, Balasuriya UB. Complex interactions between the major and minor envelope proteins of equine arteritis virus determine its tropism for equine CD3+ T lymphocytes and CD14+ monocytes. J Virol 2010 May;84(10):4898-911.
        doi: 10.1128/JVI.02743-09pubmed: 20219931google scholar: lookup
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        doi: 10.1016/s0093-691x(97)00107-6pubmed: 16728076google scholar: lookup
      5. Hedges JF, Balasuriya UB, Timoney PJ, McCollum WH, MacLachlan NJ. Genetic variation in open reading frame 2 of field isolates and laboratory strains of equine arteritis virus. Virus Res 1996 Jun;42(1-2):41-52.
        doi: 10.1016/0168-1702(96)01294-4pubmed: 8806173google scholar: lookup
      6. Chirnside ED. Equine arteritis virus: an overview. Br Vet J 1992 May-Jun;148(3):181-97.
        doi: 10.1016/0007-1935(92)90044-2pubmed: 1319787google scholar: lookup
      7. Plagemann PG, Moennig V. Lactate dehydrogenase-elevating virus, equine arteritis virus, and simian hemorrhagic fever virus: a new group of positive-strand RNA viruses. Adv Virus Res 1992;41:99-192.
        doi: 10.1016/s0065-3527(08)60036-6pubmed: 1315480google scholar: lookup