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Identification and characterization of the major pseudocoelomic proteins of the giant kidney worm, Dioctophyme renale

BACKGROUND: The giant kidney worm, Dioctophyme renale, is a debilitating and potentially lethal parasite that inhabits and destroys, typically host’s right kidney, and may also be found in ectopic sites. It is circumglobally distributed, mainly in dogs, and is increasingly regarded as a threat to ot...

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Autores principales: Giorello, A. Nahili, Kennedy, Malcolm W., Butti, Marcos J., Radman, Nilda E., Córsico, Betina, Franchini, Gisela R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5615634/
https://www.ncbi.nlm.nih.gov/pubmed/28954629
http://dx.doi.org/10.1186/s13071-017-2388-x
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author Giorello, A. Nahili
Kennedy, Malcolm W.
Butti, Marcos J.
Radman, Nilda E.
Córsico, Betina
Franchini, Gisela R.
author_facet Giorello, A. Nahili
Kennedy, Malcolm W.
Butti, Marcos J.
Radman, Nilda E.
Córsico, Betina
Franchini, Gisela R.
author_sort Giorello, A. Nahili
collection PubMed
description BACKGROUND: The giant kidney worm, Dioctophyme renale, is a debilitating and potentially lethal parasite that inhabits and destroys, typically host’s right kidney, and may also be found in ectopic sites. It is circumglobally distributed, mainly in dogs, and is increasingly regarded as a threat to other domestic animals and humans. There is little information on the parasite’s true incidence, or immune responses to it, and none on its biochemistry and molecular biology. RESULTS: We characterised the soluble proteins of body wall, intestine, gonads and pseudocelomic fluid (PCF) of adult parasites. Two proteins, P17 and P44, dominate the PCF of both male and females. P17 is of 16,622 Da by mass spectrometry, and accounts for the intense red colour of the adult parasites. It may function to carry or scavenge oxygen and be related to the ‘nemoglobins’ found in other nematode clades. P44 is of 44,460 Da and was found to associate with fatty acids by thin layer chromatography. Using environment-sensitive fluorescent lipid probes, P44 proved to be a hydrophobic ligand-binding protein with a binding site that is highly apolar, and competitive displacement experiments showed that P44 binds fatty acids. It may therefore have a role in distributing lipids within the parasites and, if also secreted, might influence local inflammatory and tissue responses. N-terminal and internal peptide amino-acid sequences of P44 indicate a relationship with a cysteine- and histidine-rich protein of unknown function from Trichinella spiralis. CONCLUSIONS: The dominant proteins of D. renale PCF are, like those of large ascaridids, likely to be involved in lipid and oxygen handling, although there is evidence of strong divergence between the two groups.
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spelling pubmed-56156342017-09-28 Identification and characterization of the major pseudocoelomic proteins of the giant kidney worm, Dioctophyme renale Giorello, A. Nahili Kennedy, Malcolm W. Butti, Marcos J. Radman, Nilda E. Córsico, Betina Franchini, Gisela R. Parasit Vectors Research BACKGROUND: The giant kidney worm, Dioctophyme renale, is a debilitating and potentially lethal parasite that inhabits and destroys, typically host’s right kidney, and may also be found in ectopic sites. It is circumglobally distributed, mainly in dogs, and is increasingly regarded as a threat to other domestic animals and humans. There is little information on the parasite’s true incidence, or immune responses to it, and none on its biochemistry and molecular biology. RESULTS: We characterised the soluble proteins of body wall, intestine, gonads and pseudocelomic fluid (PCF) of adult parasites. Two proteins, P17 and P44, dominate the PCF of both male and females. P17 is of 16,622 Da by mass spectrometry, and accounts for the intense red colour of the adult parasites. It may function to carry or scavenge oxygen and be related to the ‘nemoglobins’ found in other nematode clades. P44 is of 44,460 Da and was found to associate with fatty acids by thin layer chromatography. Using environment-sensitive fluorescent lipid probes, P44 proved to be a hydrophobic ligand-binding protein with a binding site that is highly apolar, and competitive displacement experiments showed that P44 binds fatty acids. It may therefore have a role in distributing lipids within the parasites and, if also secreted, might influence local inflammatory and tissue responses. N-terminal and internal peptide amino-acid sequences of P44 indicate a relationship with a cysteine- and histidine-rich protein of unknown function from Trichinella spiralis. CONCLUSIONS: The dominant proteins of D. renale PCF are, like those of large ascaridids, likely to be involved in lipid and oxygen handling, although there is evidence of strong divergence between the two groups. BioMed Central 2017-09-27 /pmc/articles/PMC5615634/ /pubmed/28954629 http://dx.doi.org/10.1186/s13071-017-2388-x Text en © The Author(s). 2017 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
Giorello, A. Nahili
Kennedy, Malcolm W.
Butti, Marcos J.
Radman, Nilda E.
Córsico, Betina
Franchini, Gisela R.
Identification and characterization of the major pseudocoelomic proteins of the giant kidney worm, Dioctophyme renale
title Identification and characterization of the major pseudocoelomic proteins of the giant kidney worm, Dioctophyme renale
title_full Identification and characterization of the major pseudocoelomic proteins of the giant kidney worm, Dioctophyme renale
title_fullStr Identification and characterization of the major pseudocoelomic proteins of the giant kidney worm, Dioctophyme renale
title_full_unstemmed Identification and characterization of the major pseudocoelomic proteins of the giant kidney worm, Dioctophyme renale
title_short Identification and characterization of the major pseudocoelomic proteins of the giant kidney worm, Dioctophyme renale
title_sort identification and characterization of the major pseudocoelomic proteins of the giant kidney worm, dioctophyme renale
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5615634/
https://www.ncbi.nlm.nih.gov/pubmed/28954629
http://dx.doi.org/10.1186/s13071-017-2388-x
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