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Mining nematode protein secretomes to explain lifestyle and host specificity

Parasitic nematodes are highly successful pathogens, inflicting disease on humans, animals and plants. Despite great differences in their life cycles, host preference and transmission modes, these parasites share a common capacity to manipulate their host’s immune system. This is at least partly ach...

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Autores principales: Tritten, Lucienne, Ballesteros, Cristina, Beech, Robin, Geary, Timothy G., Moreno, Yovany
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8504978/
https://www.ncbi.nlm.nih.gov/pubmed/34587193
http://dx.doi.org/10.1371/journal.pntd.0009828
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author Tritten, Lucienne
Ballesteros, Cristina
Beech, Robin
Geary, Timothy G.
Moreno, Yovany
author_facet Tritten, Lucienne
Ballesteros, Cristina
Beech, Robin
Geary, Timothy G.
Moreno, Yovany
author_sort Tritten, Lucienne
collection PubMed
description Parasitic nematodes are highly successful pathogens, inflicting disease on humans, animals and plants. Despite great differences in their life cycles, host preference and transmission modes, these parasites share a common capacity to manipulate their host’s immune system. This is at least partly achieved through the release of excretory/secretory proteins, the most well-characterized component of nematode secretomes, that are comprised of functionally diverse molecules. In this work, we analyzed published protein secretomes of parasitic nematodes to identify common patterns as well as species-specific traits. The 20 selected organisms span 4 nematode clades, including plant pathogens, animal parasites, and the free-living species Caenorhabditis elegans. Transthyretin-like proteins were the only component common to all adult secretomes; many other protein classes overlapped across multiple datasets. The glycolytic enzymes aldolase and enolase were present in all parasitic species, but missing from C. elegans. Secretomes from larval stages showed less overlap between species. Although comparison of secretome composition across species and life-cycle stages is challenged by the use of different methods and depths of sequencing among studies, our workflow enabled the identification of conserved protein families and pinpointed elements that may have evolved as to enable parasitism. This strategy, extended to more secretomes, may be exploited to prioritize therapeutic targets in the future.
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spelling pubmed-85049782021-10-12 Mining nematode protein secretomes to explain lifestyle and host specificity Tritten, Lucienne Ballesteros, Cristina Beech, Robin Geary, Timothy G. Moreno, Yovany PLoS Negl Trop Dis Research Article Parasitic nematodes are highly successful pathogens, inflicting disease on humans, animals and plants. Despite great differences in their life cycles, host preference and transmission modes, these parasites share a common capacity to manipulate their host’s immune system. This is at least partly achieved through the release of excretory/secretory proteins, the most well-characterized component of nematode secretomes, that are comprised of functionally diverse molecules. In this work, we analyzed published protein secretomes of parasitic nematodes to identify common patterns as well as species-specific traits. The 20 selected organisms span 4 nematode clades, including plant pathogens, animal parasites, and the free-living species Caenorhabditis elegans. Transthyretin-like proteins were the only component common to all adult secretomes; many other protein classes overlapped across multiple datasets. The glycolytic enzymes aldolase and enolase were present in all parasitic species, but missing from C. elegans. Secretomes from larval stages showed less overlap between species. Although comparison of secretome composition across species and life-cycle stages is challenged by the use of different methods and depths of sequencing among studies, our workflow enabled the identification of conserved protein families and pinpointed elements that may have evolved as to enable parasitism. This strategy, extended to more secretomes, may be exploited to prioritize therapeutic targets in the future. Public Library of Science 2021-09-29 /pmc/articles/PMC8504978/ /pubmed/34587193 http://dx.doi.org/10.1371/journal.pntd.0009828 Text en © 2021 Tritten et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Tritten, Lucienne
Ballesteros, Cristina
Beech, Robin
Geary, Timothy G.
Moreno, Yovany
Mining nematode protein secretomes to explain lifestyle and host specificity
title Mining nematode protein secretomes to explain lifestyle and host specificity
title_full Mining nematode protein secretomes to explain lifestyle and host specificity
title_fullStr Mining nematode protein secretomes to explain lifestyle and host specificity
title_full_unstemmed Mining nematode protein secretomes to explain lifestyle and host specificity
title_short Mining nematode protein secretomes to explain lifestyle and host specificity
title_sort mining nematode protein secretomes to explain lifestyle and host specificity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8504978/
https://www.ncbi.nlm.nih.gov/pubmed/34587193
http://dx.doi.org/10.1371/journal.pntd.0009828
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