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Time-resolved proteomic profile of Amblyomma americanum tick saliva during feeding
Amblyomma americanum ticks transmit more than a third of human tick-borne disease (TBD) agents in the United States. Tick saliva proteins are critical to success of ticks as vectors of TBD agents, and thus might serve as targets in tick antigen-based vaccines to prevent TBD infections. We describe a...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7041860/ https://www.ncbi.nlm.nih.gov/pubmed/32049966 http://dx.doi.org/10.1371/journal.pntd.0007758 |
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author | Kim, Tae Kwon Tirloni, Lucas Pinto, Antônio F. M. Diedrich, Jolene K. Moresco, James J. Yates, John R. da Silva Vaz, Itabajara Mulenga, Albert |
author_facet | Kim, Tae Kwon Tirloni, Lucas Pinto, Antônio F. M. Diedrich, Jolene K. Moresco, James J. Yates, John R. da Silva Vaz, Itabajara Mulenga, Albert |
author_sort | Kim, Tae Kwon |
collection | PubMed |
description | Amblyomma americanum ticks transmit more than a third of human tick-borne disease (TBD) agents in the United States. Tick saliva proteins are critical to success of ticks as vectors of TBD agents, and thus might serve as targets in tick antigen-based vaccines to prevent TBD infections. We describe a systems biology approach to identify, by LC-MS/MS, saliva proteins (tick = 1182, rabbit = 335) that A. americanum ticks likely inject into the host every 24 h during the first 8 days of feeding, and towards the end of feeding. Searching against entries in GenBank grouped tick and rabbit proteins into 27 and 25 functional categories. Aside from housekeeping-like proteins, majority of tick saliva proteins belong to the tick-specific (no homology to non-tick organisms: 32%), protease inhibitors (13%), proteases (8%), glycine-rich proteins (6%) and lipocalins (4%) categories. Global secretion dynamics analysis suggests that majority (74%) of proteins in this study are associated with regulating initial tick feeding functions and transmission of pathogens as they are secreted within 24–48 h of tick attachment. Comparative analysis of the A. americanum tick saliva proteome to five other tick saliva proteomes identified 284 conserved tick saliva proteins: we speculate that these regulate critical tick feeding functions and might serve as tick vaccine antigens. We discuss our findings in the context of understanding A. americanum tick feeding physiology as a means through which we can find effective targets for a vaccine against tick feeding. |
format | Online Article Text |
id | pubmed-7041860 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-70418602020-03-06 Time-resolved proteomic profile of Amblyomma americanum tick saliva during feeding Kim, Tae Kwon Tirloni, Lucas Pinto, Antônio F. M. Diedrich, Jolene K. Moresco, James J. Yates, John R. da Silva Vaz, Itabajara Mulenga, Albert PLoS Negl Trop Dis Research Article Amblyomma americanum ticks transmit more than a third of human tick-borne disease (TBD) agents in the United States. Tick saliva proteins are critical to success of ticks as vectors of TBD agents, and thus might serve as targets in tick antigen-based vaccines to prevent TBD infections. We describe a systems biology approach to identify, by LC-MS/MS, saliva proteins (tick = 1182, rabbit = 335) that A. americanum ticks likely inject into the host every 24 h during the first 8 days of feeding, and towards the end of feeding. Searching against entries in GenBank grouped tick and rabbit proteins into 27 and 25 functional categories. Aside from housekeeping-like proteins, majority of tick saliva proteins belong to the tick-specific (no homology to non-tick organisms: 32%), protease inhibitors (13%), proteases (8%), glycine-rich proteins (6%) and lipocalins (4%) categories. Global secretion dynamics analysis suggests that majority (74%) of proteins in this study are associated with regulating initial tick feeding functions and transmission of pathogens as they are secreted within 24–48 h of tick attachment. Comparative analysis of the A. americanum tick saliva proteome to five other tick saliva proteomes identified 284 conserved tick saliva proteins: we speculate that these regulate critical tick feeding functions and might serve as tick vaccine antigens. We discuss our findings in the context of understanding A. americanum tick feeding physiology as a means through which we can find effective targets for a vaccine against tick feeding. Public Library of Science 2020-02-12 /pmc/articles/PMC7041860/ /pubmed/32049966 http://dx.doi.org/10.1371/journal.pntd.0007758 Text en © 2020 Kim et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://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 Kim, Tae Kwon Tirloni, Lucas Pinto, Antônio F. M. Diedrich, Jolene K. Moresco, James J. Yates, John R. da Silva Vaz, Itabajara Mulenga, Albert Time-resolved proteomic profile of Amblyomma americanum tick saliva during feeding |
title | Time-resolved proteomic profile of Amblyomma americanum tick saliva during feeding |
title_full | Time-resolved proteomic profile of Amblyomma americanum tick saliva during feeding |
title_fullStr | Time-resolved proteomic profile of Amblyomma americanum tick saliva during feeding |
title_full_unstemmed | Time-resolved proteomic profile of Amblyomma americanum tick saliva during feeding |
title_short | Time-resolved proteomic profile of Amblyomma americanum tick saliva during feeding |
title_sort | time-resolved proteomic profile of amblyomma americanum tick saliva during feeding |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7041860/ https://www.ncbi.nlm.nih.gov/pubmed/32049966 http://dx.doi.org/10.1371/journal.pntd.0007758 |
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