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Metabolomic Analyses of Leishmania Reveal Multiple Species Differences and Large Differences in Amino Acid Metabolism

Comparative genomic analyses of Leishmania species have revealed relatively minor heterogeneity amongst recognised housekeeping genes and yet the species cause distinct infections and pathogenesis in their mammalian hosts. To gain greater information on the biochemical variation between species, and...

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Autores principales: Westrop, Gareth D., Williams, Roderick A. M., Wang, Lijie, Zhang, Tong, Watson, David G., Silva, Ana Marta, Coombs, Graham H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4569581/
https://www.ncbi.nlm.nih.gov/pubmed/26368322
http://dx.doi.org/10.1371/journal.pone.0136891
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author Westrop, Gareth D.
Williams, Roderick A. M.
Wang, Lijie
Zhang, Tong
Watson, David G.
Silva, Ana Marta
Coombs, Graham H.
author_facet Westrop, Gareth D.
Williams, Roderick A. M.
Wang, Lijie
Zhang, Tong
Watson, David G.
Silva, Ana Marta
Coombs, Graham H.
author_sort Westrop, Gareth D.
collection PubMed
description Comparative genomic analyses of Leishmania species have revealed relatively minor heterogeneity amongst recognised housekeeping genes and yet the species cause distinct infections and pathogenesis in their mammalian hosts. To gain greater information on the biochemical variation between species, and insights into possible metabolic mechanisms underpinning visceral and cutaneous leishmaniasis, we have undertaken in this study a comparative analysis of the metabolomes of promastigotes of L. donovani, L. major and L. mexicana. The analysis revealed 64 metabolites with confirmed identity differing 3-fold or more between the cell extracts of species, with 161 putatively identified metabolites differing similarly. Analysis of the media from cultures revealed an at least 3-fold difference in use or excretion of 43 metabolites of confirmed identity and 87 putatively identified metabolites that differed to a similar extent. Strikingly large differences were detected in their extent of amino acid use and metabolism, especially for tryptophan, aspartate, arginine and proline. Major pathways of tryptophan and arginine catabolism were shown to be to indole-3-lactate and arginic acid, respectively, which were excreted. The data presented provide clear evidence on the value of global metabolomic analyses in detecting species-specific metabolic features, thus application of this technology should be a major contributor to gaining greater understanding of how pathogens are adapted to infecting their hosts.
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spelling pubmed-45695812015-09-18 Metabolomic Analyses of Leishmania Reveal Multiple Species Differences and Large Differences in Amino Acid Metabolism Westrop, Gareth D. Williams, Roderick A. M. Wang, Lijie Zhang, Tong Watson, David G. Silva, Ana Marta Coombs, Graham H. PLoS One Research Article Comparative genomic analyses of Leishmania species have revealed relatively minor heterogeneity amongst recognised housekeeping genes and yet the species cause distinct infections and pathogenesis in their mammalian hosts. To gain greater information on the biochemical variation between species, and insights into possible metabolic mechanisms underpinning visceral and cutaneous leishmaniasis, we have undertaken in this study a comparative analysis of the metabolomes of promastigotes of L. donovani, L. major and L. mexicana. The analysis revealed 64 metabolites with confirmed identity differing 3-fold or more between the cell extracts of species, with 161 putatively identified metabolites differing similarly. Analysis of the media from cultures revealed an at least 3-fold difference in use or excretion of 43 metabolites of confirmed identity and 87 putatively identified metabolites that differed to a similar extent. Strikingly large differences were detected in their extent of amino acid use and metabolism, especially for tryptophan, aspartate, arginine and proline. Major pathways of tryptophan and arginine catabolism were shown to be to indole-3-lactate and arginic acid, respectively, which were excreted. The data presented provide clear evidence on the value of global metabolomic analyses in detecting species-specific metabolic features, thus application of this technology should be a major contributor to gaining greater understanding of how pathogens are adapted to infecting their hosts. Public Library of Science 2015-09-14 /pmc/articles/PMC4569581/ /pubmed/26368322 http://dx.doi.org/10.1371/journal.pone.0136891 Text en © 2015 Westrop 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Westrop, Gareth D.
Williams, Roderick A. M.
Wang, Lijie
Zhang, Tong
Watson, David G.
Silva, Ana Marta
Coombs, Graham H.
Metabolomic Analyses of Leishmania Reveal Multiple Species Differences and Large Differences in Amino Acid Metabolism
title Metabolomic Analyses of Leishmania Reveal Multiple Species Differences and Large Differences in Amino Acid Metabolism
title_full Metabolomic Analyses of Leishmania Reveal Multiple Species Differences and Large Differences in Amino Acid Metabolism
title_fullStr Metabolomic Analyses of Leishmania Reveal Multiple Species Differences and Large Differences in Amino Acid Metabolism
title_full_unstemmed Metabolomic Analyses of Leishmania Reveal Multiple Species Differences and Large Differences in Amino Acid Metabolism
title_short Metabolomic Analyses of Leishmania Reveal Multiple Species Differences and Large Differences in Amino Acid Metabolism
title_sort metabolomic analyses of leishmania reveal multiple species differences and large differences in amino acid metabolism
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4569581/
https://www.ncbi.nlm.nih.gov/pubmed/26368322
http://dx.doi.org/10.1371/journal.pone.0136891
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