Antibodies and PMBC from EIAV infected carrier horses recognize gp45 and p26 synthetic peptides.
Abstract: Equine infectious anemia virus (EIAV) is a lentivirus causing a persistent infection in horses characterized by recurrent febrile episodes and high levels of viremia associated with a novel antigenic strain of the virus. The virus contains two envelope glycoproteins, gp90 and gp45, and four internal proteins, p26, p15, p11 and p9. Considering that the most infected horses are able to restrict EIAV replication to very low levels and that gp45 and p26 contain highly conserved epitopes among lentiviruses, it would be necessary to identify those conserved epitopes stimulating cellular and humoral responses. The aims of this study were to determine if the synthetic peptides identified as gp45 (aa 523-547) and p26 (aa 318-346) representing two highly conserved and immunodominant regions of EIA virus are recognized by PBMC and antibodies to EIAV adult mixed-breed naturally infected carrier horses, and if these peptides are able to induce immune responses in mice. Antibodies from 100% of carrier horses, evaluated by ELISA, recognized both peptides; PBMC from 80% of carrier horses, evaluated by lymphoproliferation assay, recognized, at least, one peptide. Furthermore, immunization with 100 microg of each peptide elicited humoral and cellular responses in BALB/c mice, antibodies appeared at 48 or 63 days of immunization with gp45 or p26, respectively. Although the kinetics of gp45- and p26-specific antibody responses were similar, percentage of positivity was higher for gp45. The lymphoproliferation assay, evaluated by BrdU uptake, was higher in mice immunized with gp45 or p26 than in the control group (P<0.05). Based on our findings, we consider that both peptides could be included in an effective vaccine design to induce long-term immunological memory.
Publication Date: 2005-08-18 PubMed ID: 16105689DOI: 10.1016/j.vetimm.2005.06.007Google Scholar: Lookup
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- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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The study investigates the effectiveness of two synthetic proteins, gp45 and p26, found in Equine infectious anemia virus (EIAV) in inducing immune responses in horses and mice. It found that both proteins were recognized by the immune system and could provoke an immune response, indicating their potential use in vaccine design.
Understanding EIAV and its Proteins
- The study focuses on Equine infectious anemia virus (EIAV), a lentivirus that causes a persistent infection in horses marked by recurring fevers and high levels of viremia (viruses circulating in the blood) associated with a new antigenic strain of the virus.
- The virus is made up of six proteins, with the study specifically focusing on two of them; an envelope glycoprotein gp45, and an internal protein p26.
Identification of Potential Immune Stimulators
- The researchers sought to identify the conserved epitopes (part of an antigen that is recognized by the immune system) in the two proteins that could stimulate both the humoral (antibody-mediated) and cellular (cell-mediated) immune responses.
- This is based on the observation that most infected horses can restrict EIAV replication to low levels and that the proteins gp45 and p26 carry highly conserved epitopes among lentiviruses.
Results of the Study
- Antibodies from all evaluated carrier horses recognized both gp45 and p26 peptides.
- Peripheral blood mononuclear cells (PBMC) from 80% of carrier horses responded to at least one peptide.
- BALB/c mice immunized with each of the peptides developed a humoral and cellular response. The antibodies were present 48 days and 63 days post immunization with gp45 or p26, respectively, with a higher positivity rate for gp45.
- The lymphoproliferation (increase in the number of lymphocytes, normal constituents of blood and important in the immune system) was higher in immunized mice than the control group, suggesting that the peptides helped stimulate this increase.
Implications for Vaccine Design
- These results suggest that both peptides gp45 and p26 could be included in effective vaccine design to induce long-term immunological memory, which would provide immunity against the virus.
- Further research is needed to understand the implications of these findings to vaccine design and to test the real-world effectiveness of such a vaccine.
Cite This Article
APA
Soutullo A, García MI, Bailat A, Racca A, Tonarelli G, Malan Borel I.
(2005).
Antibodies and PMBC from EIAV infected carrier horses recognize gp45 and p26 synthetic peptides.
Vet Immunol Immunopathol, 108(3-4), 335-343.
https://doi.org/10.1016/j.vetimm.2005.06.007 Publication
Researcher Affiliations
- Laboratorio de Inmunoquímica, Dirección de Sanidad Animal, Ministerio de la Producción, Bv. Pellegrini 3100, Santa Fe, Argentina.
MeSH Terms
- Amino Acid Sequence
- Animals
- Antibodies, Viral / immunology
- Carrier State / immunology
- Carrier State / veterinary
- Equine Infectious Anemia / immunology
- Female
- Horses / immunology
- Mice
- Mice, Inbred BALB C
- Neutrophils / immunology
- Spleen / cytology
- Time Factors
- Viral Core Proteins / immunology
- Viral Envelope Proteins / immunology
Citations
This article has been cited 1 times.- Romo-Sáenz CI, Tamez-Guerra P, Olivas-Holguin A, Ramos-Zayas Y, Obregón-Macías N, González-Ochoa G, Zavala-Díaz de la Serna FJ, Rodríguez-Padilla C, Tamez-Guerra R, Gomez-Flores R. Molecular detection of equine infectious anemia virus in clinically normal, seronegative horses in an endemic area of Mexico.. J Vet Diagn Invest 2021 Jul;33(4):758-761.
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