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Analysis of the mitochondrial maxicircle of Trypanosoma lewisi, a neglected human pathogen

BACKGROUND: The haemoflagellate Trypanosoma lewisi is a kinetoplastid parasite which, as it has been recently reported to cause human disease, deserves increased attention. Characteristic features of all kinetoplastid flagellates are a uniquely structured mitochondrial DNA or kinetoplast, comprised...

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Autores principales: Lin, Ruo-Hong, Lai, De-Hua, Zheng, Ling-Ling, Wu, Jie, Lukeš, Julius, Hide, Geoff, Lun, Zhao-Rong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4696184/
https://www.ncbi.nlm.nih.gov/pubmed/26715306
http://dx.doi.org/10.1186/s13071-015-1281-8
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author Lin, Ruo-Hong
Lai, De-Hua
Zheng, Ling-Ling
Wu, Jie
Lukeš, Julius
Hide, Geoff
Lun, Zhao-Rong
author_facet Lin, Ruo-Hong
Lai, De-Hua
Zheng, Ling-Ling
Wu, Jie
Lukeš, Julius
Hide, Geoff
Lun, Zhao-Rong
author_sort Lin, Ruo-Hong
collection PubMed
description BACKGROUND: The haemoflagellate Trypanosoma lewisi is a kinetoplastid parasite which, as it has been recently reported to cause human disease, deserves increased attention. Characteristic features of all kinetoplastid flagellates are a uniquely structured mitochondrial DNA or kinetoplast, comprised of a network of catenated DNA circles, and RNA editing of mitochondrial transcripts. The aim of this study was to describe the kinetoplast DNA of T. lewisi. METHODS/RESULTS: In this study, purified kinetoplast DNA from T. lewisi was sequenced using high-throughput sequencing in combination with sequencing of PCR amplicons. This allowed the assembly of the T. lewisi kinetoplast maxicircle DNA, which is a homologue of the mitochondrial genome in other eukaryotes. The assembly of 23,745 bp comprises the non-coding and coding regions. Comparative analysis of the maxicircle sequence of T. lewisi with Trypanosoma cruzi, Trypanosoma rangeli, Trypanosoma brucei and Leishmania tarentolae revealed that it shares 78 %, 77 %, 74 % and 66 % sequence identity with these parasites, respectively. The high GC content in at least 9 maxicircle genes of T. lewisi (ATPase6; NADH dehydrogenase subunits ND3, ND7, ND8 and ND9; G-rich regions GR3 and GR4; cytochrome oxidase subunit COIII and ribosomal protein RPS12) implies that their products may be extensively edited. A detailed analysis of the non-coding region revealed that it contains numerous repeat motifs and palindromes. CONCLUSIONS: We have sequenced and comprehensively annotated the kinetoplast maxicircle of T. lewisi. Our analysis reveals that T. lewisi is closely related to T. cruzi and T. brucei, and may share similar RNA editing patterns with them rather than with L. tarentolae. These findings provide novel insight into the biological features of this emerging human pathogen. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13071-015-1281-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-46961842015-12-31 Analysis of the mitochondrial maxicircle of Trypanosoma lewisi, a neglected human pathogen Lin, Ruo-Hong Lai, De-Hua Zheng, Ling-Ling Wu, Jie Lukeš, Julius Hide, Geoff Lun, Zhao-Rong Parasit Vectors Research BACKGROUND: The haemoflagellate Trypanosoma lewisi is a kinetoplastid parasite which, as it has been recently reported to cause human disease, deserves increased attention. Characteristic features of all kinetoplastid flagellates are a uniquely structured mitochondrial DNA or kinetoplast, comprised of a network of catenated DNA circles, and RNA editing of mitochondrial transcripts. The aim of this study was to describe the kinetoplast DNA of T. lewisi. METHODS/RESULTS: In this study, purified kinetoplast DNA from T. lewisi was sequenced using high-throughput sequencing in combination with sequencing of PCR amplicons. This allowed the assembly of the T. lewisi kinetoplast maxicircle DNA, which is a homologue of the mitochondrial genome in other eukaryotes. The assembly of 23,745 bp comprises the non-coding and coding regions. Comparative analysis of the maxicircle sequence of T. lewisi with Trypanosoma cruzi, Trypanosoma rangeli, Trypanosoma brucei and Leishmania tarentolae revealed that it shares 78 %, 77 %, 74 % and 66 % sequence identity with these parasites, respectively. The high GC content in at least 9 maxicircle genes of T. lewisi (ATPase6; NADH dehydrogenase subunits ND3, ND7, ND8 and ND9; G-rich regions GR3 and GR4; cytochrome oxidase subunit COIII and ribosomal protein RPS12) implies that their products may be extensively edited. A detailed analysis of the non-coding region revealed that it contains numerous repeat motifs and palindromes. CONCLUSIONS: We have sequenced and comprehensively annotated the kinetoplast maxicircle of T. lewisi. Our analysis reveals that T. lewisi is closely related to T. cruzi and T. brucei, and may share similar RNA editing patterns with them rather than with L. tarentolae. These findings provide novel insight into the biological features of this emerging human pathogen. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13071-015-1281-8) contains supplementary material, which is available to authorized users. BioMed Central 2015-12-30 /pmc/articles/PMC4696184/ /pubmed/26715306 http://dx.doi.org/10.1186/s13071-015-1281-8 Text en © Lin et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Lin, Ruo-Hong
Lai, De-Hua
Zheng, Ling-Ling
Wu, Jie
Lukeš, Julius
Hide, Geoff
Lun, Zhao-Rong
Analysis of the mitochondrial maxicircle of Trypanosoma lewisi, a neglected human pathogen
title Analysis of the mitochondrial maxicircle of Trypanosoma lewisi, a neglected human pathogen
title_full Analysis of the mitochondrial maxicircle of Trypanosoma lewisi, a neglected human pathogen
title_fullStr Analysis of the mitochondrial maxicircle of Trypanosoma lewisi, a neglected human pathogen
title_full_unstemmed Analysis of the mitochondrial maxicircle of Trypanosoma lewisi, a neglected human pathogen
title_short Analysis of the mitochondrial maxicircle of Trypanosoma lewisi, a neglected human pathogen
title_sort analysis of the mitochondrial maxicircle of trypanosoma lewisi, a neglected human pathogen
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4696184/
https://www.ncbi.nlm.nih.gov/pubmed/26715306
http://dx.doi.org/10.1186/s13071-015-1281-8
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