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Immunocontraceptive potential of a GnRH receptor-based fusion recombinant protein
BACKGROUND: The management of stray dog population has been of utmost importance due to their overpopulation, increase in dog bites incidence, and rabies. Contraceptive vaccines, a non-surgical alternative to spaying and neutering are viewed as a valuable option for the management of dog population....
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8096874/ https://www.ncbi.nlm.nih.gov/pubmed/33945047 http://dx.doi.org/10.1186/s43141-021-00164-9 |
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author | Sandam, Nathaniel Philip Prakash, Dhamodhar Thimmareddy, Prashanth |
author_facet | Sandam, Nathaniel Philip Prakash, Dhamodhar Thimmareddy, Prashanth |
author_sort | Sandam, Nathaniel Philip |
collection | PubMed |
description | BACKGROUND: The management of stray dog population has been of utmost importance due to their overpopulation, increase in dog bites incidence, and rabies. Contraceptive vaccines, a non-surgical alternative to spaying and neutering are viewed as a valuable option for the management of dog population. In this study, the contraceptive potential of a recombinant fusion protein containing the three genes GnRH, GnRH receptor, and ZP3 was explored. RESULTS: The gene fragment encoding GnRH, GnRHR, and ZP3 along with the antigenic epitopes of canine distemper virus and tetanus toxoid was assembled, synthesized, and cloned into pET28a expression vector. The resulting construct GVAC08 was successfully transformed into BL21DE3 strain of E. coli and confirmed by colony PCR. The recombinant GVAC08 protein was expressed and purified using Ni-NTA and was confirmed to be a 50-KDa protein by SDS PAGE and Western blot. Mice were immunized with the GVAC08 protein using Freund’s complete adjuvant followed by a booster using Freund’s incomplete adjuvant. This induced a high antibody titer against GnRH, GnRH receptor, and ZP3 which was determined by ELISA. CONCLUSION: Mating studies showed that the GVAC08 recombinant protein was able to reduce the litter size in immunized mice showing improved efficacy. However, the vaccine candidate with further improvements will be a viable contraceptive vaccine. |
format | Online Article Text |
id | pubmed-8096874 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-80968742021-05-18 Immunocontraceptive potential of a GnRH receptor-based fusion recombinant protein Sandam, Nathaniel Philip Prakash, Dhamodhar Thimmareddy, Prashanth J Genet Eng Biotechnol Research BACKGROUND: The management of stray dog population has been of utmost importance due to their overpopulation, increase in dog bites incidence, and rabies. Contraceptive vaccines, a non-surgical alternative to spaying and neutering are viewed as a valuable option for the management of dog population. In this study, the contraceptive potential of a recombinant fusion protein containing the three genes GnRH, GnRH receptor, and ZP3 was explored. RESULTS: The gene fragment encoding GnRH, GnRHR, and ZP3 along with the antigenic epitopes of canine distemper virus and tetanus toxoid was assembled, synthesized, and cloned into pET28a expression vector. The resulting construct GVAC08 was successfully transformed into BL21DE3 strain of E. coli and confirmed by colony PCR. The recombinant GVAC08 protein was expressed and purified using Ni-NTA and was confirmed to be a 50-KDa protein by SDS PAGE and Western blot. Mice were immunized with the GVAC08 protein using Freund’s complete adjuvant followed by a booster using Freund’s incomplete adjuvant. This induced a high antibody titer against GnRH, GnRH receptor, and ZP3 which was determined by ELISA. CONCLUSION: Mating studies showed that the GVAC08 recombinant protein was able to reduce the litter size in immunized mice showing improved efficacy. However, the vaccine candidate with further improvements will be a viable contraceptive vaccine. Springer Berlin Heidelberg 2021-05-04 /pmc/articles/PMC8096874/ /pubmed/33945047 http://dx.doi.org/10.1186/s43141-021-00164-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Sandam, Nathaniel Philip Prakash, Dhamodhar Thimmareddy, Prashanth Immunocontraceptive potential of a GnRH receptor-based fusion recombinant protein |
title | Immunocontraceptive potential of a GnRH receptor-based fusion recombinant protein |
title_full | Immunocontraceptive potential of a GnRH receptor-based fusion recombinant protein |
title_fullStr | Immunocontraceptive potential of a GnRH receptor-based fusion recombinant protein |
title_full_unstemmed | Immunocontraceptive potential of a GnRH receptor-based fusion recombinant protein |
title_short | Immunocontraceptive potential of a GnRH receptor-based fusion recombinant protein |
title_sort | immunocontraceptive potential of a gnrh receptor-based fusion recombinant protein |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8096874/ https://www.ncbi.nlm.nih.gov/pubmed/33945047 http://dx.doi.org/10.1186/s43141-021-00164-9 |
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