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CAP protein superfamily members in Toxocara canis

BACKGROUND: Proteins of the cysteine-rich secretory proteins, antigen 5 and pathogenesis-related 1 (CAP) superfamily are recognized or proposed to play roles in parasite development and reproduction, and in modulating host immune attack and infection processes. However, little is known about these p...

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Autores principales: Stroehlein, Andreas J., Young, Neil D., Hall, Ross S., Korhonen, Pasi K., Hofmann, Andreas, Sternberg, Paul W., Jabbar, Abdul, Gasser, Robin B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4921028/
https://www.ncbi.nlm.nih.gov/pubmed/27342979
http://dx.doi.org/10.1186/s13071-016-1642-y
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author Stroehlein, Andreas J.
Young, Neil D.
Hall, Ross S.
Korhonen, Pasi K.
Hofmann, Andreas
Sternberg, Paul W.
Jabbar, Abdul
Gasser, Robin B.
author_facet Stroehlein, Andreas J.
Young, Neil D.
Hall, Ross S.
Korhonen, Pasi K.
Hofmann, Andreas
Sternberg, Paul W.
Jabbar, Abdul
Gasser, Robin B.
author_sort Stroehlein, Andreas J.
collection PubMed
description BACKGROUND: Proteins of the cysteine-rich secretory proteins, antigen 5 and pathogenesis-related 1 (CAP) superfamily are recognized or proposed to play roles in parasite development and reproduction, and in modulating host immune attack and infection processes. However, little is known about these proteins for most parasites. RESULTS: In the present study, we explored CAP proteins of Toxocara canis, a socioeconomically important zoonotic roundworm. To do this, we mined and curated transcriptomic and genomic data, predicted and curated full-length protein sequences (n = 28), conducted analyses of these data and studied the transcription of respective genes in different developmental stages of T. canis. In addition, based on information available for Caenorhabditis elegans, we inferred that selected genes (including lon-1, vap-1, vap-2, scl-1, scl-8 and scl-11 orthologs) of T. canis and their interaction partners likely play central roles in this parasite’s development and/or reproduction via TGF-beta and/or insulin-like signaling pathways, or via host interactions. CONCLUSION: In conclusion, this study could provide a foundation to guide future studies of CAP proteins of T. canis and related parasites, and might assist in finding new interventions against diseases caused by these parasites. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13071-016-1642-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-49210282016-06-26 CAP protein superfamily members in Toxocara canis Stroehlein, Andreas J. Young, Neil D. Hall, Ross S. Korhonen, Pasi K. Hofmann, Andreas Sternberg, Paul W. Jabbar, Abdul Gasser, Robin B. Parasit Vectors Research BACKGROUND: Proteins of the cysteine-rich secretory proteins, antigen 5 and pathogenesis-related 1 (CAP) superfamily are recognized or proposed to play roles in parasite development and reproduction, and in modulating host immune attack and infection processes. However, little is known about these proteins for most parasites. RESULTS: In the present study, we explored CAP proteins of Toxocara canis, a socioeconomically important zoonotic roundworm. To do this, we mined and curated transcriptomic and genomic data, predicted and curated full-length protein sequences (n = 28), conducted analyses of these data and studied the transcription of respective genes in different developmental stages of T. canis. In addition, based on information available for Caenorhabditis elegans, we inferred that selected genes (including lon-1, vap-1, vap-2, scl-1, scl-8 and scl-11 orthologs) of T. canis and their interaction partners likely play central roles in this parasite’s development and/or reproduction via TGF-beta and/or insulin-like signaling pathways, or via host interactions. CONCLUSION: In conclusion, this study could provide a foundation to guide future studies of CAP proteins of T. canis and related parasites, and might assist in finding new interventions against diseases caused by these parasites. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13071-016-1642-y) contains supplementary material, which is available to authorized users. BioMed Central 2016-06-24 /pmc/articles/PMC4921028/ /pubmed/27342979 http://dx.doi.org/10.1186/s13071-016-1642-y Text en © The Author(s). 2016 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
Stroehlein, Andreas J.
Young, Neil D.
Hall, Ross S.
Korhonen, Pasi K.
Hofmann, Andreas
Sternberg, Paul W.
Jabbar, Abdul
Gasser, Robin B.
CAP protein superfamily members in Toxocara canis
title CAP protein superfamily members in Toxocara canis
title_full CAP protein superfamily members in Toxocara canis
title_fullStr CAP protein superfamily members in Toxocara canis
title_full_unstemmed CAP protein superfamily members in Toxocara canis
title_short CAP protein superfamily members in Toxocara canis
title_sort cap protein superfamily members in toxocara canis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4921028/
https://www.ncbi.nlm.nih.gov/pubmed/27342979
http://dx.doi.org/10.1186/s13071-016-1642-y
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