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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....

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Autores principales: Sandam, Nathaniel Philip, Prakash, Dhamodhar, Thimmareddy, Prashanth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
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.
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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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