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

被引:3
作者
Geerts, Manon [1 ,4 ,5 ]
Chen, Zihao [2 ]
Bebronne, Nicolas [1 ]
Savill, Nicholas J. [2 ]
Schnaufer, Achim [2 ]
Buscher, Philippe [1 ]
Van Reet, Nick [1 ]
Van den Broeck, Frederik [1 ,3 ]
机构
[1] Inst Trop Med, Dept Biomed Sci, B-2000 Antwerp, Belgium
[2] Univ Edinburgh, Inst Immunol & Infect Res, Edinburgh EH9 3FL, Midlothian, Scotland
[3] Katholieke Univ Leuven, Rega Inst Med Res, Dept Microbiol Immunol & Transplantat, B-3000 Leuven, Belgium
[4] Katholieke Univ Leuven, Fish Eco Evo Devo & Conservat, B-3000 Leuven, Belgium
[5] Royal Belgian Inst Nat Sci, Directorate Taxon & Phylogeny, B-1000 Brussels, Belgium
基金
英国生物技术与生命科学研究理事会; 比尔及梅琳达.盖茨基金会; 英国医学研究理事会;
关键词
SLEEPING SICKNESS; CONSERVED SEQUENCE; DNA MINICIRCLES; ORGANIZATION; IDENTIFICATION; PCR; CLONALITY; DIVERSITY; EVOLUTION; PARENTS;
D O I
10.1093/nargab/lqac081
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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.
引用
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页数:14
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