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Identification and evaluation of vaccine candidate antigens from the poultry red mite (Dermanyssus gallinae)

An aqueous extract of the haematophagous poultry ectoparasite, Dermanyssus gallinae, was subfractionated using anion exchange chromatography. Six of these subfractions were used to immunise hens and the blood from these hens was fed, in vitro, to poultry red mites. Mite mortality following these fee...

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Autores principales: Bartley, Kathryn, Wright, Harry W., Huntley, John F., Manson, Erin D.T., Inglis, Neil F., McLean, Kevin, Nath, Mintu, Bartley, Yvonne, Nisbet, Alasdair J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4655837/
https://www.ncbi.nlm.nih.gov/pubmed/26296690
http://dx.doi.org/10.1016/j.ijpara.2015.07.004
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author Bartley, Kathryn
Wright, Harry W.
Huntley, John F.
Manson, Erin D.T.
Inglis, Neil F.
McLean, Kevin
Nath, Mintu
Bartley, Yvonne
Nisbet, Alasdair J.
author_facet Bartley, Kathryn
Wright, Harry W.
Huntley, John F.
Manson, Erin D.T.
Inglis, Neil F.
McLean, Kevin
Nath, Mintu
Bartley, Yvonne
Nisbet, Alasdair J.
author_sort Bartley, Kathryn
collection PubMed
description An aqueous extract of the haematophagous poultry ectoparasite, Dermanyssus gallinae, was subfractionated using anion exchange chromatography. Six of these subfractions were used to immunise hens and the blood from these hens was fed, in vitro, to poultry red mites. Mite mortality following these feeds was indicative of protective antigens in two of the subfractions, with the risks of mites dying being 3.1 and 3.7 times higher than in the control group (P < 0.001). A combination of two-dimensional immunoblotting and immunoaffinity chromatography, using IgY from hens immunised with these subfractions, was used in concert with proteomic analyses to identify the strongest immunogenic proteins in each of these subfractions. Ten of the immunoreactive proteins were selected for assessment as vaccine candidates using the following criteria: intensity of immune recognition; likelihood of exposure of the antigen to the antibodies in a blood meal; proposed function and known vaccine potential of orthologous molecules. Recombinant versions of each of these 10 proteins were produced in Escherichia coli and were used to immunise hens. Subsequent in vitro feeding of mites on blood from these birds indicated that immunisation with Deg-SRP-1 (serpin), Deg-VIT-1 (vitellogenin), Deg-HGP-1 (hemelipoglycoprotein) or Deg-PUF-1 (a protein of unknown function) resulted in significantly increased risk of mite death (1.7–2.8 times higher than in mites fed blood from control hens immunised with adjuvant only, P < 0.001). The potential for using these antigens in a recombinant vaccine is discussed.
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spelling pubmed-46558372015-12-18 Identification and evaluation of vaccine candidate antigens from the poultry red mite (Dermanyssus gallinae) Bartley, Kathryn Wright, Harry W. Huntley, John F. Manson, Erin D.T. Inglis, Neil F. McLean, Kevin Nath, Mintu Bartley, Yvonne Nisbet, Alasdair J. Int J Parasitol Article An aqueous extract of the haematophagous poultry ectoparasite, Dermanyssus gallinae, was subfractionated using anion exchange chromatography. Six of these subfractions were used to immunise hens and the blood from these hens was fed, in vitro, to poultry red mites. Mite mortality following these feeds was indicative of protective antigens in two of the subfractions, with the risks of mites dying being 3.1 and 3.7 times higher than in the control group (P < 0.001). A combination of two-dimensional immunoblotting and immunoaffinity chromatography, using IgY from hens immunised with these subfractions, was used in concert with proteomic analyses to identify the strongest immunogenic proteins in each of these subfractions. Ten of the immunoreactive proteins were selected for assessment as vaccine candidates using the following criteria: intensity of immune recognition; likelihood of exposure of the antigen to the antibodies in a blood meal; proposed function and known vaccine potential of orthologous molecules. Recombinant versions of each of these 10 proteins were produced in Escherichia coli and were used to immunise hens. Subsequent in vitro feeding of mites on blood from these birds indicated that immunisation with Deg-SRP-1 (serpin), Deg-VIT-1 (vitellogenin), Deg-HGP-1 (hemelipoglycoprotein) or Deg-PUF-1 (a protein of unknown function) resulted in significantly increased risk of mite death (1.7–2.8 times higher than in mites fed blood from control hens immunised with adjuvant only, P < 0.001). The potential for using these antigens in a recombinant vaccine is discussed. Elsevier Science 2015-11 /pmc/articles/PMC4655837/ /pubmed/26296690 http://dx.doi.org/10.1016/j.ijpara.2015.07.004 Text en © 2015 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Bartley, Kathryn
Wright, Harry W.
Huntley, John F.
Manson, Erin D.T.
Inglis, Neil F.
McLean, Kevin
Nath, Mintu
Bartley, Yvonne
Nisbet, Alasdair J.
Identification and evaluation of vaccine candidate antigens from the poultry red mite (Dermanyssus gallinae)
title Identification and evaluation of vaccine candidate antigens from the poultry red mite (Dermanyssus gallinae)
title_full Identification and evaluation of vaccine candidate antigens from the poultry red mite (Dermanyssus gallinae)
title_fullStr Identification and evaluation of vaccine candidate antigens from the poultry red mite (Dermanyssus gallinae)
title_full_unstemmed Identification and evaluation of vaccine candidate antigens from the poultry red mite (Dermanyssus gallinae)
title_short Identification and evaluation of vaccine candidate antigens from the poultry red mite (Dermanyssus gallinae)
title_sort identification and evaluation of vaccine candidate antigens from the poultry red mite (dermanyssus gallinae)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4655837/
https://www.ncbi.nlm.nih.gov/pubmed/26296690
http://dx.doi.org/10.1016/j.ijpara.2015.07.004
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