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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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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. |
format | Online Article Text |
id | pubmed-4921028 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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