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 partl...

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Autores principales: Lucienne Tritten, Cristina Ballesteros, Robin Beech, Timothy G Geary, Yovany Moreno
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Publicado: Public Library of Science (PLoS) 2021
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spelling oai:doaj.org-article:b69745fa329f4bf79a314a4a958105982021-12-02T20:24:00ZMining nematode protein secretomes to explain lifestyle and host specificity.1935-27271935-273510.1371/journal.pntd.0009828https://doaj.org/article/b69745fa329f4bf79a314a4a958105982021-09-01T00:00:00Zhttps://doi.org/10.1371/journal.pntd.0009828https://doaj.org/toc/1935-2727https://doaj.org/toc/1935-2735Parasitic 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.Lucienne TrittenCristina BallesterosRobin BeechTimothy G GearyYovany MorenoPublic Library of Science (PLoS)articleArctic medicine. Tropical medicineRC955-962Public aspects of medicineRA1-1270ENPLoS Neglected Tropical Diseases, Vol 15, Iss 9, p e0009828 (2021)
institution DOAJ
collection DOAJ
language EN
topic Arctic medicine. Tropical medicine
RC955-962
Public aspects of medicine
RA1-1270
spellingShingle Arctic medicine. Tropical medicine
RC955-962
Public aspects of medicine
RA1-1270
Lucienne Tritten
Cristina Ballesteros
Robin Beech
Timothy G Geary
Yovany Moreno
Mining nematode protein secretomes to explain lifestyle and host specificity.
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.
format article
author Lucienne Tritten
Cristina Ballesteros
Robin Beech
Timothy G Geary
Yovany Moreno
author_facet Lucienne Tritten
Cristina Ballesteros
Robin Beech
Timothy G Geary
Yovany Moreno
author_sort Lucienne Tritten
title Mining nematode protein secretomes to explain lifestyle and host specificity.
title_short 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_sort mining nematode protein secretomes to explain lifestyle and host specificity.
publisher Public Library of Science (PLoS)
publishDate 2021
url https://doaj.org/article/b69745fa329f4bf79a314a4a95810598
work_keys_str_mv AT luciennetritten miningnematodeproteinsecretomestoexplainlifestyleandhostspecificity
AT cristinaballesteros miningnematodeproteinsecretomestoexplainlifestyleandhostspecificity
AT robinbeech miningnematodeproteinsecretomestoexplainlifestyleandhostspecificity
AT timothyggeary miningnematodeproteinsecretomestoexplainlifestyleandhostspecificity
AT yovanymoreno miningnematodeproteinsecretomestoexplainlifestyleandhostspecificity
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