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Spatial metabolomics identifies localized chemical changes in heart tissue during chronic cardiac Chagas Disease

Chagas disease (CD), caused by the parasite Trypanosoma cruzi, is one of nineteen neglected tropical diseases. CD is a vector-borne disease transmitted by triatomines, but CD can also be transmitted through blood transfusions, organ transplants, T. cruzi-contaminated food and drinks, and congenital...

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Autores principales: Dean, Danya A., Gautham, Gautham, Siqueira-Neto, Jair L., McKerrow, James H., Dorrestein, Pieter C., McCall, Laura-Isobel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8516257/
https://www.ncbi.nlm.nih.gov/pubmed/34606502
http://dx.doi.org/10.1371/journal.pntd.0009819
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author Dean, Danya A.
Gautham, Gautham
Siqueira-Neto, Jair L.
McKerrow, James H.
Dorrestein, Pieter C.
McCall, Laura-Isobel
author_facet Dean, Danya A.
Gautham, Gautham
Siqueira-Neto, Jair L.
McKerrow, James H.
Dorrestein, Pieter C.
McCall, Laura-Isobel
author_sort Dean, Danya A.
collection PubMed
description Chagas disease (CD), caused by the parasite Trypanosoma cruzi, is one of nineteen neglected tropical diseases. CD is a vector-borne disease transmitted by triatomines, but CD can also be transmitted through blood transfusions, organ transplants, T. cruzi-contaminated food and drinks, and congenital transmission. While endemic to the Americas, T. cruzi infects 7–8 million people worldwide and can induce severe cardiac symptoms including apical aneurysms, thromboembolisms and arrhythmias during the chronic stage of CD. However, these cardiac clinical manifestations and CD pathogenesis are not fully understood. Using spatial metabolomics (chemical cartography), we sought to understand the localized impact of chronic CD on the cardiac metabolome of mice infected with two divergent T. cruzi strains. Our data showed chemical differences in localized cardiac regions upon chronic T. cruzi infection, indicating that parasite infection changes the host metabolome at specific sites in chronic CD. These sites were distinct from the sites of highest parasite burden. In addition, we identified acylcarnitines and glycerophosphocholines as discriminatory chemical families within each heart region, comparing infected and uninfected samples. Overall, our study indicated global and positional metabolic differences common to infection with different T. cruzi strains and identified select infection-modulated pathways. These results provide further insight into CD pathogenesis and demonstrate the advantage of a systematic spatial perspective to understand infectious disease tropism.
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spelling pubmed-85162572021-10-15 Spatial metabolomics identifies localized chemical changes in heart tissue during chronic cardiac Chagas Disease Dean, Danya A. Gautham, Gautham Siqueira-Neto, Jair L. McKerrow, James H. Dorrestein, Pieter C. McCall, Laura-Isobel PLoS Negl Trop Dis Research Article Chagas disease (CD), caused by the parasite Trypanosoma cruzi, is one of nineteen neglected tropical diseases. CD is a vector-borne disease transmitted by triatomines, but CD can also be transmitted through blood transfusions, organ transplants, T. cruzi-contaminated food and drinks, and congenital transmission. While endemic to the Americas, T. cruzi infects 7–8 million people worldwide and can induce severe cardiac symptoms including apical aneurysms, thromboembolisms and arrhythmias during the chronic stage of CD. However, these cardiac clinical manifestations and CD pathogenesis are not fully understood. Using spatial metabolomics (chemical cartography), we sought to understand the localized impact of chronic CD on the cardiac metabolome of mice infected with two divergent T. cruzi strains. Our data showed chemical differences in localized cardiac regions upon chronic T. cruzi infection, indicating that parasite infection changes the host metabolome at specific sites in chronic CD. These sites were distinct from the sites of highest parasite burden. In addition, we identified acylcarnitines and glycerophosphocholines as discriminatory chemical families within each heart region, comparing infected and uninfected samples. Overall, our study indicated global and positional metabolic differences common to infection with different T. cruzi strains and identified select infection-modulated pathways. These results provide further insight into CD pathogenesis and demonstrate the advantage of a systematic spatial perspective to understand infectious disease tropism. Public Library of Science 2021-10-04 /pmc/articles/PMC8516257/ /pubmed/34606502 http://dx.doi.org/10.1371/journal.pntd.0009819 Text en © 2021 Dean 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
Dean, Danya A.
Gautham, Gautham
Siqueira-Neto, Jair L.
McKerrow, James H.
Dorrestein, Pieter C.
McCall, Laura-Isobel
Spatial metabolomics identifies localized chemical changes in heart tissue during chronic cardiac Chagas Disease
title Spatial metabolomics identifies localized chemical changes in heart tissue during chronic cardiac Chagas Disease
title_full Spatial metabolomics identifies localized chemical changes in heart tissue during chronic cardiac Chagas Disease
title_fullStr Spatial metabolomics identifies localized chemical changes in heart tissue during chronic cardiac Chagas Disease
title_full_unstemmed Spatial metabolomics identifies localized chemical changes in heart tissue during chronic cardiac Chagas Disease
title_short Spatial metabolomics identifies localized chemical changes in heart tissue during chronic cardiac Chagas Disease
title_sort spatial metabolomics identifies localized chemical changes in heart tissue during chronic cardiac chagas disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8516257/
https://www.ncbi.nlm.nih.gov/pubmed/34606502
http://dx.doi.org/10.1371/journal.pntd.0009819
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