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Virology2010; 410(1); 96-106; doi: 10.1016/j.virol.2010.10.032

A proviral derivative from a reference attenuated EIAV vaccine strain failed to elicit protective immunity.

Abstract: To investigate essential factors that determine the efficacy of vaccines against lentiviruses, an effective attenuated equine infectious anemia virus (EIAV) vaccine strain and a proviral derivative of the vaccine were compared with respect to differences in inducing protective immunity. Although these two strains replicated equally well in vitro and in vivo, the proviral strain induced significantly less protection from disease and infection caused by viral challenge and significantly lower specific neutralizing capability. These findings indicated that the proviral strain had lost the ability to stimulate immune protection compared to the parental vaccine strain. A further analysis of the envelope gp90 gene variation revealed that compared to the proviral strain, the vaccine strain displayed a wide sequence diversity in immunogen composition. Thus, we inferred that the differences in immunogen composition might be the major cause for the failure of the proviral derivative to elicit the immune protection induced by the parental strain.
Publication Date: 2010-11-20 PubMed ID: 21094511DOI: 10.1016/j.virol.2010.10.032Google Scholar: Lookup
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  • Journal Article
  • Randomized Controlled Trial
  • Research Support
  • Non-U.S. Gov't

Summary

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The study discovered that a proviral strain of equine infectious anemia virus (EIAV) was not as effective as a traditional vaccine strain in providing protection against the disease, suggesting variations in immunogen composition could influence vaccine efficacy.

Comparing Attenuated EIAV Vaccine Strain and Proviral Derivative

  • The research aimed to draw a contrast between the EIAV vaccine strain and its proviral derivative, in terms of their efficiency in evoking immune protection. The investigation helps in understanding the significant factors that determine the capability of vaccines to combat lentiviruses.
  • Both these strains replicated equally well when tested in vitro (outside a living organism) and in vivo (within a living organism). However, the proviral strain was associated with notably lower protection from disease and infection after exposure to a viral challenge.
  • The proviral strain also displayed a significantly lower neutralizing capability, pointing to its diminished ability to arouse effective immune protection in comparison to the original vaccine strain.

Analyzing Envelope gp90 Gene Variation

  • A deeper examination of the variation in the envelope gp90 gene, a critical part of the virus that interacts with the host’s immune system, was conducted. This gene’s variation can potentially affect the efficiency of the vaccine strain. In other words, the variation may render a particular strain either successful or unsuccessful in provoking immune protection.
  • The vaccine strain demonstrated a wider sequence diversity in immunogen composition when compared to the proviral strain. This means that the proviral strain is not as genetically diverse as the vaccine strain, at least in term of the gp90 gene.

Impact of Variation in Immunogen Composition

  • From the observations made in this research, it was concluded that the major cause of failure of the proviral derivative to induce immune protection like its parental strain (the EIAV vaccine) might be the variations in immunogen composition. Immunogens are substances that provoke an immune response.
  • This suggests that preserving a broad level of genetic diversity, particularly in regards to the envelope gp90 gene and immunogen composition, may be critical for maintaining the effectiveness of a vaccine.

Cite This Article

APA
Ma J, Shi N, Jiang CG, Lin YZ, Wang XF, Wang S, Lv XL, Zhao LP, Shao YM, Kong XG, Zhou JH, Shen RX. (2010). A proviral derivative from a reference attenuated EIAV vaccine strain failed to elicit protective immunity. Virology, 410(1), 96-106. https://doi.org/10.1016/j.virol.2010.10.032

Publication

ISSN: 1096-0341
NlmUniqueID: 0110674
Country: United States
Language: English
Volume: 410
Issue: 1
Pages: 96-106

Researcher Affiliations

Ma, Jian
  • State Key Laboratory of Veterinary Biotechnology, Division of Livestock Diseases, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin, China.
Shi, Nan
    Jiang, Cheng-Gang
      Lin, Yue-Zhi
        Wang, Xue-Feng
          Wang, Shuai
            Lv, Xiao-Ling
              Zhao, Li-Ping
                Shao, Yi-Ming
                  Kong, Xian-Gang
                    Zhou, Jian-Hua
                      Shen, Rong-Xian

                        MeSH Terms

                        • Animals
                        • Antibodies, Viral
                        • Cloning, Molecular
                        • Equine Infectious Anemia / prevention & control
                        • Equine Infectious Anemia / virology
                        • Female
                        • Horses
                        • Infectious Anemia Virus, Equine / genetics
                        • Infectious Anemia Virus, Equine / immunology
                        • Infectious Anemia Virus, Equine / pathogenicity
                        • Male
                        • Proviruses / immunology
                        • Vaccines, Attenuated
                        • Viral Load
                        • Viral Vaccines
                        • Virulence

                        Citations

                        This article has been cited 14 times.
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