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Identification of anti-horn fly vaccine antigen candidates using a reverse vaccinology approach

BACKGROUND: The horn fly, Haematobia irritans irritans, causes significant production losses to the cattle industry. Horn fly control relies on insecticides; however, alternative control methods such as vaccines are needed due to the fly's capacity to quickly develop resistance to insecticides,...

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Autores principales: Domingues, Luísa N., Bendele, Kylie G., Halos, Lénaïg, Moreno, Yovany, Epe, Christian, Figueiredo, Monica, Liebstein, Martin, Guerrero, Felix D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8414034/
https://www.ncbi.nlm.nih.gov/pubmed/34479607
http://dx.doi.org/10.1186/s13071-021-04938-5
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author Domingues, Luísa N.
Bendele, Kylie G.
Halos, Lénaïg
Moreno, Yovany
Epe, Christian
Figueiredo, Monica
Liebstein, Martin
Guerrero, Felix D.
author_facet Domingues, Luísa N.
Bendele, Kylie G.
Halos, Lénaïg
Moreno, Yovany
Epe, Christian
Figueiredo, Monica
Liebstein, Martin
Guerrero, Felix D.
author_sort Domingues, Luísa N.
collection PubMed
description BACKGROUND: The horn fly, Haematobia irritans irritans, causes significant production losses to the cattle industry. Horn fly control relies on insecticides; however, alternative control methods such as vaccines are needed due to the fly's capacity to quickly develop resistance to insecticides, and the pressure for eco-friendly options. METHODS: We used a reverse vaccinology approach comprising three vaccine prediction and 11 annotation tools to evaluate and rank 79,542 translated open reading frames (ORFs) from the horn fly's transcriptome, and selected 10 transcript ORFs as vaccine candidates for expression in Pichia pastoris. The expression of the 10 selected transcripts and the proteins that they encoded were investigated in adult flies by reverse transcription polymerase chain reaction (RT-PCR) and mass spectrometry, respectively. Then, we evaluated the immunogenicity of a vaccine candidate in an immunization trial and the antigen’s effects on horn fly mortality and fecundity in an in vitro feeding assay. RESULTS: Six of the ten vaccine candidate antigens were successfully expressed in P. pastoris. RT-PCR confirmed the expression of all six ORFs in adult fly RNA. One of the vaccine candidate antigens, BI-HS009, was expressed in sufficient quantity for immunogenicity and efficacy trials. The IgG titers of animals vaccinated with BI-HS009 plus adjuvant were significantly higher than those of animals vaccinated with buffer plus adjuvant only from days 42 to 112, with a peak on day 56. Progeny of horn flies feeding upon blood from animals vaccinated with BI-HS009 plus adjuvant collected on day 56 had 63% lower pupariation rate and 57% lower adult emergence than the control group (ANOVA: F ((1, 6)) = 8.221, P = 0.028 and F ((1, 6)) = 8.299, P = 0.028, respectively). CONCLUSIONS: The reverse vaccinology approach streamlined the discovery process by prioritizing possible vaccine antigen candidates. Through a thoughtful process of selection and in vivo and in vitro evaluations, we were able to identify a promising antigen for an anti-horn fly vaccine. GRAPHICAL ABSTRACT: SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13071-021-04938-5.
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spelling pubmed-84140342021-09-03 Identification of anti-horn fly vaccine antigen candidates using a reverse vaccinology approach Domingues, Luísa N. Bendele, Kylie G. Halos, Lénaïg Moreno, Yovany Epe, Christian Figueiredo, Monica Liebstein, Martin Guerrero, Felix D. Parasit Vectors Research BACKGROUND: The horn fly, Haematobia irritans irritans, causes significant production losses to the cattle industry. Horn fly control relies on insecticides; however, alternative control methods such as vaccines are needed due to the fly's capacity to quickly develop resistance to insecticides, and the pressure for eco-friendly options. METHODS: We used a reverse vaccinology approach comprising three vaccine prediction and 11 annotation tools to evaluate and rank 79,542 translated open reading frames (ORFs) from the horn fly's transcriptome, and selected 10 transcript ORFs as vaccine candidates for expression in Pichia pastoris. The expression of the 10 selected transcripts and the proteins that they encoded were investigated in adult flies by reverse transcription polymerase chain reaction (RT-PCR) and mass spectrometry, respectively. Then, we evaluated the immunogenicity of a vaccine candidate in an immunization trial and the antigen’s effects on horn fly mortality and fecundity in an in vitro feeding assay. RESULTS: Six of the ten vaccine candidate antigens were successfully expressed in P. pastoris. RT-PCR confirmed the expression of all six ORFs in adult fly RNA. One of the vaccine candidate antigens, BI-HS009, was expressed in sufficient quantity for immunogenicity and efficacy trials. The IgG titers of animals vaccinated with BI-HS009 plus adjuvant were significantly higher than those of animals vaccinated with buffer plus adjuvant only from days 42 to 112, with a peak on day 56. Progeny of horn flies feeding upon blood from animals vaccinated with BI-HS009 plus adjuvant collected on day 56 had 63% lower pupariation rate and 57% lower adult emergence than the control group (ANOVA: F ((1, 6)) = 8.221, P = 0.028 and F ((1, 6)) = 8.299, P = 0.028, respectively). CONCLUSIONS: The reverse vaccinology approach streamlined the discovery process by prioritizing possible vaccine antigen candidates. Through a thoughtful process of selection and in vivo and in vitro evaluations, we were able to identify a promising antigen for an anti-horn fly vaccine. GRAPHICAL ABSTRACT: SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13071-021-04938-5. BioMed Central 2021-09-03 /pmc/articles/PMC8414034/ /pubmed/34479607 http://dx.doi.org/10.1186/s13071-021-04938-5 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Domingues, Luísa N.
Bendele, Kylie G.
Halos, Lénaïg
Moreno, Yovany
Epe, Christian
Figueiredo, Monica
Liebstein, Martin
Guerrero, Felix D.
Identification of anti-horn fly vaccine antigen candidates using a reverse vaccinology approach
title Identification of anti-horn fly vaccine antigen candidates using a reverse vaccinology approach
title_full Identification of anti-horn fly vaccine antigen candidates using a reverse vaccinology approach
title_fullStr Identification of anti-horn fly vaccine antigen candidates using a reverse vaccinology approach
title_full_unstemmed Identification of anti-horn fly vaccine antigen candidates using a reverse vaccinology approach
title_short Identification of anti-horn fly vaccine antigen candidates using a reverse vaccinology approach
title_sort identification of anti-horn fly vaccine antigen candidates using a reverse vaccinology approach
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8414034/
https://www.ncbi.nlm.nih.gov/pubmed/34479607
http://dx.doi.org/10.1186/s13071-021-04938-5
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