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Deep kinetoplast genome analyses result in a novel molecular assay for detecting Trypanosoma brucei gambiense-specific minicircles

The World Health Organization targeted Trypanosoma brucei gambiense (Tbg) human African trypanosomiasis for elimination of transmission by 2030. Sensitive molecular markers that specifically detect Tbg type 1 (Tbg1) parasites will be important tools to assist in reaching this goal. We aim at improvi...

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Autores principales: Geerts, Manon, Chen, Zihao, Bebronne, Nicolas, Savill, Nicholas J, Schnaufer, Achim, Büscher, Philippe, Van Reet, Nick, Van den Broeck, Frederik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9582789/
https://www.ncbi.nlm.nih.gov/pubmed/36285287
http://dx.doi.org/10.1093/nargab/lqac081
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author Geerts, Manon
Chen, Zihao
Bebronne, Nicolas
Savill, Nicholas J
Schnaufer, Achim
Büscher, Philippe
Van Reet, Nick
Van den Broeck, Frederik
author_facet Geerts, Manon
Chen, Zihao
Bebronne, Nicolas
Savill, Nicholas J
Schnaufer, Achim
Büscher, Philippe
Van Reet, Nick
Van den Broeck, Frederik
author_sort Geerts, Manon
collection PubMed
description The World Health Organization targeted Trypanosoma brucei gambiense (Tbg) human African trypanosomiasis for elimination of transmission by 2030. Sensitive molecular markers that specifically detect Tbg type 1 (Tbg1) parasites will be important tools to assist in reaching this goal. We aim at improving molecular diagnosis of Tbg1 infections by targeting the abundant mitochondrial minicircles within the kinetoplast of these parasites. Using Next-Generation Sequencing of total cellular DNA extracts, we assembled and annotated the kinetoplast genome and investigated minicircle sequence diversity in 38 animal- and human-infective trypanosome strains. Computational analyses recognized a total of 241 Minicircle Sequence Classes as Tbg1-specific, of which three were shared by the 18 studied Tbg1 strains. We developed a minicircle-based assay that is applicable on animals and as specific as the TgsGP-based assay, the current golden standard for molecular detection of Tbg1. The median copy number of the targeted minicircle was equal to eight, suggesting our minicircle-based assay may be used for the sensitive detection of Tbg1 parasites. Annotation of the targeted minicircle sequence indicated that it encodes genes essential for the survival of the parasite and will thus likely be preserved in natural Tbg1 populations, the latter ensuring the reliability of our novel diagnostic assay.
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spelling pubmed-95827892022-10-24 Deep kinetoplast genome analyses result in a novel molecular assay for detecting Trypanosoma brucei gambiense-specific minicircles Geerts, Manon Chen, Zihao Bebronne, Nicolas Savill, Nicholas J Schnaufer, Achim Büscher, Philippe Van Reet, Nick Van den Broeck, Frederik NAR Genom Bioinform Standard Article The World Health Organization targeted Trypanosoma brucei gambiense (Tbg) human African trypanosomiasis for elimination of transmission by 2030. Sensitive molecular markers that specifically detect Tbg type 1 (Tbg1) parasites will be important tools to assist in reaching this goal. We aim at improving molecular diagnosis of Tbg1 infections by targeting the abundant mitochondrial minicircles within the kinetoplast of these parasites. Using Next-Generation Sequencing of total cellular DNA extracts, we assembled and annotated the kinetoplast genome and investigated minicircle sequence diversity in 38 animal- and human-infective trypanosome strains. Computational analyses recognized a total of 241 Minicircle Sequence Classes as Tbg1-specific, of which three were shared by the 18 studied Tbg1 strains. We developed a minicircle-based assay that is applicable on animals and as specific as the TgsGP-based assay, the current golden standard for molecular detection of Tbg1. The median copy number of the targeted minicircle was equal to eight, suggesting our minicircle-based assay may be used for the sensitive detection of Tbg1 parasites. Annotation of the targeted minicircle sequence indicated that it encodes genes essential for the survival of the parasite and will thus likely be preserved in natural Tbg1 populations, the latter ensuring the reliability of our novel diagnostic assay. Oxford University Press 2022-10-20 /pmc/articles/PMC9582789/ /pubmed/36285287 http://dx.doi.org/10.1093/nargab/lqac081 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of NAR Genomics and Bioinformatics. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Standard Article
Geerts, Manon
Chen, Zihao
Bebronne, Nicolas
Savill, Nicholas J
Schnaufer, Achim
Büscher, Philippe
Van Reet, Nick
Van den Broeck, Frederik
Deep kinetoplast genome analyses result in a novel molecular assay for detecting Trypanosoma brucei gambiense-specific minicircles
title Deep kinetoplast genome analyses result in a novel molecular assay for detecting Trypanosoma brucei gambiense-specific minicircles
title_full Deep kinetoplast genome analyses result in a novel molecular assay for detecting Trypanosoma brucei gambiense-specific minicircles
title_fullStr Deep kinetoplast genome analyses result in a novel molecular assay for detecting Trypanosoma brucei gambiense-specific minicircles
title_full_unstemmed Deep kinetoplast genome analyses result in a novel molecular assay for detecting Trypanosoma brucei gambiense-specific minicircles
title_short Deep kinetoplast genome analyses result in a novel molecular assay for detecting Trypanosoma brucei gambiense-specific minicircles
title_sort deep kinetoplast genome analyses result in a novel molecular assay for detecting trypanosoma brucei gambiense-specific minicircles
topic Standard Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9582789/
https://www.ncbi.nlm.nih.gov/pubmed/36285287
http://dx.doi.org/10.1093/nargab/lqac081
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