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A genomic analysis and transcriptomic atlas of gene expression in Psoroptes ovis reveals feeding- and stage-specific patterns of allergen expression

BACKGROUND: Psoroptic mange, caused by infestation with the ectoparasitic mite, Psoroptes ovis, is highly contagious, resulting in intense pruritus and represents a major welfare and economic concern for the livestock industry Worldwide. Control relies on injectable endectocides and organophosphate...

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Autores principales: Burgess, Stewart T. G., Marr, Edward J., Bartley, Kathryn, Nunn, Francesca G., Down, Rachel E., Weaver, Robert J., Prickett, Jessica C., Dunn, Jackie, Rombauts, Stephane, Van Leeuwen, Thomas, Van de Peer, Yves, Nisbet, Alasdair J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6806590/
https://www.ncbi.nlm.nih.gov/pubmed/31640546
http://dx.doi.org/10.1186/s12864-019-6082-6
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author Burgess, Stewart T. G.
Marr, Edward J.
Bartley, Kathryn
Nunn, Francesca G.
Down, Rachel E.
Weaver, Robert J.
Prickett, Jessica C.
Dunn, Jackie
Rombauts, Stephane
Van Leeuwen, Thomas
Van de Peer, Yves
Nisbet, Alasdair J.
author_facet Burgess, Stewart T. G.
Marr, Edward J.
Bartley, Kathryn
Nunn, Francesca G.
Down, Rachel E.
Weaver, Robert J.
Prickett, Jessica C.
Dunn, Jackie
Rombauts, Stephane
Van Leeuwen, Thomas
Van de Peer, Yves
Nisbet, Alasdair J.
author_sort Burgess, Stewart T. G.
collection PubMed
description BACKGROUND: Psoroptic mange, caused by infestation with the ectoparasitic mite, Psoroptes ovis, is highly contagious, resulting in intense pruritus and represents a major welfare and economic concern for the livestock industry Worldwide. Control relies on injectable endectocides and organophosphate dips, but concerns over residues, environmental contamination, and the development of resistance threaten the sustainability of this approach, highlighting interest in alternative control methods. However, development of vaccines and identification of chemotherapeutic targets is hampered by the lack of P. ovis transcriptomic and genomic resources. RESULTS: Building on the recent publication of the P. ovis draft genome, here we present a genomic analysis and transcriptomic atlas of gene expression in P. ovis revealing feeding- and stage-specific patterns of gene expression, including novel multigene families and allergens. Network-based clustering revealed 14 gene clusters demonstrating either single- or multi-stage specific gene expression patterns, with 3075 female-specific, 890 male-specific and 112, 217 and 526 transcripts showing larval, protonymph and tritonymph specific-expression, respectively. Detailed analysis of P. ovis allergens revealed stage-specific patterns of allergen gene expression, many of which were also enriched in “fed” mites and tritonymphs, highlighting an important feeding-related allergenicity in this developmental stage. Pair-wise analysis of differential expression between life-cycle stages identified patterns of sex-biased gene expression and also identified novel P. ovis multigene families including known allergens and novel genes with high levels of stage-specific expression. CONCLUSIONS: The genomic and transcriptomic atlas described here represents a unique resource for the acarid-research community, whilst the OrcAE platform makes this freely available, facilitating further community-led curation of the draft P. ovis genome.
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spelling pubmed-68065902019-10-28 A genomic analysis and transcriptomic atlas of gene expression in Psoroptes ovis reveals feeding- and stage-specific patterns of allergen expression Burgess, Stewart T. G. Marr, Edward J. Bartley, Kathryn Nunn, Francesca G. Down, Rachel E. Weaver, Robert J. Prickett, Jessica C. Dunn, Jackie Rombauts, Stephane Van Leeuwen, Thomas Van de Peer, Yves Nisbet, Alasdair J. BMC Genomics Research Article BACKGROUND: Psoroptic mange, caused by infestation with the ectoparasitic mite, Psoroptes ovis, is highly contagious, resulting in intense pruritus and represents a major welfare and economic concern for the livestock industry Worldwide. Control relies on injectable endectocides and organophosphate dips, but concerns over residues, environmental contamination, and the development of resistance threaten the sustainability of this approach, highlighting interest in alternative control methods. However, development of vaccines and identification of chemotherapeutic targets is hampered by the lack of P. ovis transcriptomic and genomic resources. RESULTS: Building on the recent publication of the P. ovis draft genome, here we present a genomic analysis and transcriptomic atlas of gene expression in P. ovis revealing feeding- and stage-specific patterns of gene expression, including novel multigene families and allergens. Network-based clustering revealed 14 gene clusters demonstrating either single- or multi-stage specific gene expression patterns, with 3075 female-specific, 890 male-specific and 112, 217 and 526 transcripts showing larval, protonymph and tritonymph specific-expression, respectively. Detailed analysis of P. ovis allergens revealed stage-specific patterns of allergen gene expression, many of which were also enriched in “fed” mites and tritonymphs, highlighting an important feeding-related allergenicity in this developmental stage. Pair-wise analysis of differential expression between life-cycle stages identified patterns of sex-biased gene expression and also identified novel P. ovis multigene families including known allergens and novel genes with high levels of stage-specific expression. CONCLUSIONS: The genomic and transcriptomic atlas described here represents a unique resource for the acarid-research community, whilst the OrcAE platform makes this freely available, facilitating further community-led curation of the draft P. ovis genome. BioMed Central 2019-10-23 /pmc/articles/PMC6806590/ /pubmed/31640546 http://dx.doi.org/10.1186/s12864-019-6082-6 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Burgess, Stewart T. G.
Marr, Edward J.
Bartley, Kathryn
Nunn, Francesca G.
Down, Rachel E.
Weaver, Robert J.
Prickett, Jessica C.
Dunn, Jackie
Rombauts, Stephane
Van Leeuwen, Thomas
Van de Peer, Yves
Nisbet, Alasdair J.
A genomic analysis and transcriptomic atlas of gene expression in Psoroptes ovis reveals feeding- and stage-specific patterns of allergen expression
title A genomic analysis and transcriptomic atlas of gene expression in Psoroptes ovis reveals feeding- and stage-specific patterns of allergen expression
title_full A genomic analysis and transcriptomic atlas of gene expression in Psoroptes ovis reveals feeding- and stage-specific patterns of allergen expression
title_fullStr A genomic analysis and transcriptomic atlas of gene expression in Psoroptes ovis reveals feeding- and stage-specific patterns of allergen expression
title_full_unstemmed A genomic analysis and transcriptomic atlas of gene expression in Psoroptes ovis reveals feeding- and stage-specific patterns of allergen expression
title_short A genomic analysis and transcriptomic atlas of gene expression in Psoroptes ovis reveals feeding- and stage-specific patterns of allergen expression
title_sort genomic analysis and transcriptomic atlas of gene expression in psoroptes ovis reveals feeding- and stage-specific patterns of allergen expression
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6806590/
https://www.ncbi.nlm.nih.gov/pubmed/31640546
http://dx.doi.org/10.1186/s12864-019-6082-6
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