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DNA Vaccines Against Mycoplasma Elicit Humoral Immune Responses in Ostriches
In ostriches, the population densities resulting from intensive rearing increases susceptibility to pathogens such as mycoplasmas. In addition to good management practices, vaccination offers an attractive alternative for controlling mycoplasma infections in food animals, instead of using antibiotic...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6527592/ https://www.ncbi.nlm.nih.gov/pubmed/31139188 http://dx.doi.org/10.3389/fimmu.2019.01061 |
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author | Wium, Martha Jonker, Hester Isabella Olivier, Adriaan Jacobus Bellstedt, Dirk Uwe Botes, Annelise |
author_facet | Wium, Martha Jonker, Hester Isabella Olivier, Adriaan Jacobus Bellstedt, Dirk Uwe Botes, Annelise |
author_sort | Wium, Martha |
collection | PubMed |
description | In ostriches, the population densities resulting from intensive rearing increases susceptibility to pathogens such as mycoplasmas. In addition to good management practices, vaccination offers an attractive alternative for controlling mycoplasma infections in food animals, instead of using antibiotics, which often leave unacceptable residues. The use of live attenuated vaccines, however, carry the concern of reversion to virulence or genetic recombination with field strains. Currently there are no commercially available vaccines against ostrich-infecting mycoplasmas and this study therefore set out to develop and evaluate the use of a DNA vaccine against mycoplasma infections in ostriches using an OppA protein as antigen. To this end, the oppA gene of “Mycoplasma nasistruthionis sp. nov.” str. Ms03 was cloned into two DNA vaccine expression vectors after codon correction by site-directed mutagenesis. Three-months-old ostriches were then vaccinated intramuscularly at different doses followed by a booster vaccination after 6 weeks. The ability of the DNA vaccines to elicit an anti-OppA antibody response was evaluated by ELISA using the recombinant OppA protein of Ms03 as coating antigen. A statistically significant anti-OppA antibody response could be detected after administration of a booster vaccination indicating that the OppA protein was successfully immunogenic. The responses were also both dose and vector dependent. In conclusion, the DNA vaccines were able to elicit an immune response in ostriches and can therefore be viewed as an option for the development of vaccines against mycoplasma infections. |
format | Online Article Text |
id | pubmed-6527592 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65275922019-05-28 DNA Vaccines Against Mycoplasma Elicit Humoral Immune Responses in Ostriches Wium, Martha Jonker, Hester Isabella Olivier, Adriaan Jacobus Bellstedt, Dirk Uwe Botes, Annelise Front Immunol Immunology In ostriches, the population densities resulting from intensive rearing increases susceptibility to pathogens such as mycoplasmas. In addition to good management practices, vaccination offers an attractive alternative for controlling mycoplasma infections in food animals, instead of using antibiotics, which often leave unacceptable residues. The use of live attenuated vaccines, however, carry the concern of reversion to virulence or genetic recombination with field strains. Currently there are no commercially available vaccines against ostrich-infecting mycoplasmas and this study therefore set out to develop and evaluate the use of a DNA vaccine against mycoplasma infections in ostriches using an OppA protein as antigen. To this end, the oppA gene of “Mycoplasma nasistruthionis sp. nov.” str. Ms03 was cloned into two DNA vaccine expression vectors after codon correction by site-directed mutagenesis. Three-months-old ostriches were then vaccinated intramuscularly at different doses followed by a booster vaccination after 6 weeks. The ability of the DNA vaccines to elicit an anti-OppA antibody response was evaluated by ELISA using the recombinant OppA protein of Ms03 as coating antigen. A statistically significant anti-OppA antibody response could be detected after administration of a booster vaccination indicating that the OppA protein was successfully immunogenic. The responses were also both dose and vector dependent. In conclusion, the DNA vaccines were able to elicit an immune response in ostriches and can therefore be viewed as an option for the development of vaccines against mycoplasma infections. Frontiers Media S.A. 2019-05-14 /pmc/articles/PMC6527592/ /pubmed/31139188 http://dx.doi.org/10.3389/fimmu.2019.01061 Text en Copyright © 2019 Wium, Jonker, Olivier, Bellstedt and Botes. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Wium, Martha Jonker, Hester Isabella Olivier, Adriaan Jacobus Bellstedt, Dirk Uwe Botes, Annelise DNA Vaccines Against Mycoplasma Elicit Humoral Immune Responses in Ostriches |
title | DNA Vaccines Against Mycoplasma Elicit Humoral Immune Responses in Ostriches |
title_full | DNA Vaccines Against Mycoplasma Elicit Humoral Immune Responses in Ostriches |
title_fullStr | DNA Vaccines Against Mycoplasma Elicit Humoral Immune Responses in Ostriches |
title_full_unstemmed | DNA Vaccines Against Mycoplasma Elicit Humoral Immune Responses in Ostriches |
title_short | DNA Vaccines Against Mycoplasma Elicit Humoral Immune Responses in Ostriches |
title_sort | dna vaccines against mycoplasma elicit humoral immune responses in ostriches |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6527592/ https://www.ncbi.nlm.nih.gov/pubmed/31139188 http://dx.doi.org/10.3389/fimmu.2019.01061 |
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