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Chagas disease vector blood meal sources identified by protein mass spectrometry

Chagas disease is a complex vector borne parasitic disease involving blood feeding Triatominae (Hemiptera: Reduviidae) insects, also known as kissing bugs, and the vertebrates they feed on. This disease has tremendous impacts on millions of people and is a global health problem. The etiological agen...

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Autores principales: Keller, Judith I., Ballif, Bryan A., St. Clair, Riley M., Vincent, James J., Monroy, M. Carlota, Stevens, Lori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5726658/
https://www.ncbi.nlm.nih.gov/pubmed/29232402
http://dx.doi.org/10.1371/journal.pone.0189647
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author Keller, Judith I.
Ballif, Bryan A.
St. Clair, Riley M.
Vincent, James J.
Monroy, M. Carlota
Stevens, Lori
author_facet Keller, Judith I.
Ballif, Bryan A.
St. Clair, Riley M.
Vincent, James J.
Monroy, M. Carlota
Stevens, Lori
author_sort Keller, Judith I.
collection PubMed
description Chagas disease is a complex vector borne parasitic disease involving blood feeding Triatominae (Hemiptera: Reduviidae) insects, also known as kissing bugs, and the vertebrates they feed on. This disease has tremendous impacts on millions of people and is a global health problem. The etiological agent of Chagas disease, Trypanosoma cruzi (Kinetoplastea: Trypanosomatida: Trypanosomatidae), is deposited on the mammalian host in the insect’s feces during a blood meal, and enters the host’s blood stream through mucous membranes or a break in the skin. Identifying the blood meal sources of triatomine vectors is critical in understanding Chagas disease transmission dynamics, can lead to identification of other vertebrates important in the transmission cycle, and aids management decisions. The latter is particularly important as there is little in the way of effective therapeutics for Chagas disease. Several techniques, mostly DNA-based, are available for blood meal identification. However, further methods are needed, particularly when sample conditions lead to low-quality DNA or to assess the risk of human cross-contamination. We demonstrate a proteomics-based approach, using liquid chromatography tandem mass spectrometry (LC-MS/MS) to identify host-specific hemoglobin peptides for blood meal identification in mouse blood control samples and apply LC-MS/MS for the first time to Triatoma dimidiata insect vectors, tracing blood sources to species. In contrast to most proteins, hemoglobin, stabilized by iron, is incredibly stable even being preserved through geologic time. We compared blood stored with and without an anticoagulant and examined field-collected insect specimens stored in suboptimal conditions such as at room temperature for long periods of time. To our knowledge, this is the first study using LC-MS/MS on field-collected arthropod disease vectors to identify blood meal composition, and where blood meal identification was confirmed with more traditional DNA-based methods. We also demonstrate the potential of synthetic peptide standards to estimate relative amounts of hemoglobin acquired when insects feed on multiple blood sources. These LC-MS/MS methods can contribute to developing Ecohealth control strategies for Chagas disease transmission and can be applied to other arthropod disease vectors.
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spelling pubmed-57266582017-12-22 Chagas disease vector blood meal sources identified by protein mass spectrometry Keller, Judith I. Ballif, Bryan A. St. Clair, Riley M. Vincent, James J. Monroy, M. Carlota Stevens, Lori PLoS One Research Article Chagas disease is a complex vector borne parasitic disease involving blood feeding Triatominae (Hemiptera: Reduviidae) insects, also known as kissing bugs, and the vertebrates they feed on. This disease has tremendous impacts on millions of people and is a global health problem. The etiological agent of Chagas disease, Trypanosoma cruzi (Kinetoplastea: Trypanosomatida: Trypanosomatidae), is deposited on the mammalian host in the insect’s feces during a blood meal, and enters the host’s blood stream through mucous membranes or a break in the skin. Identifying the blood meal sources of triatomine vectors is critical in understanding Chagas disease transmission dynamics, can lead to identification of other vertebrates important in the transmission cycle, and aids management decisions. The latter is particularly important as there is little in the way of effective therapeutics for Chagas disease. Several techniques, mostly DNA-based, are available for blood meal identification. However, further methods are needed, particularly when sample conditions lead to low-quality DNA or to assess the risk of human cross-contamination. We demonstrate a proteomics-based approach, using liquid chromatography tandem mass spectrometry (LC-MS/MS) to identify host-specific hemoglobin peptides for blood meal identification in mouse blood control samples and apply LC-MS/MS for the first time to Triatoma dimidiata insect vectors, tracing blood sources to species. In contrast to most proteins, hemoglobin, stabilized by iron, is incredibly stable even being preserved through geologic time. We compared blood stored with and without an anticoagulant and examined field-collected insect specimens stored in suboptimal conditions such as at room temperature for long periods of time. To our knowledge, this is the first study using LC-MS/MS on field-collected arthropod disease vectors to identify blood meal composition, and where blood meal identification was confirmed with more traditional DNA-based methods. We also demonstrate the potential of synthetic peptide standards to estimate relative amounts of hemoglobin acquired when insects feed on multiple blood sources. These LC-MS/MS methods can contribute to developing Ecohealth control strategies for Chagas disease transmission and can be applied to other arthropod disease vectors. Public Library of Science 2017-12-12 /pmc/articles/PMC5726658/ /pubmed/29232402 http://dx.doi.org/10.1371/journal.pone.0189647 Text en © 2017 Keller 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
Keller, Judith I.
Ballif, Bryan A.
St. Clair, Riley M.
Vincent, James J.
Monroy, M. Carlota
Stevens, Lori
Chagas disease vector blood meal sources identified by protein mass spectrometry
title Chagas disease vector blood meal sources identified by protein mass spectrometry
title_full Chagas disease vector blood meal sources identified by protein mass spectrometry
title_fullStr Chagas disease vector blood meal sources identified by protein mass spectrometry
title_full_unstemmed Chagas disease vector blood meal sources identified by protein mass spectrometry
title_short Chagas disease vector blood meal sources identified by protein mass spectrometry
title_sort chagas disease vector blood meal sources identified by protein mass spectrometry
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5726658/
https://www.ncbi.nlm.nih.gov/pubmed/29232402
http://dx.doi.org/10.1371/journal.pone.0189647
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