Deep kinetoplast genome analyses result in a novel molecular assay for detecting Trypanosoma brucei gambiense-specific minicircles. Issue 4 (20th October 2022)

• Record Type: Journal Article
• Authors: Geerts, Manon; Chen, Zihao; Bebronne, Nicolas; Savill, Nicholas J; Schnaufer, Achim; Büscher, Philippe; Van Reet, Nick; Van den Broeck, Frederik
• Is Part Of: NAR genomics and bioinformatics. Volume 4:Issue 4(2022)
• Publication Date: 2022-10-20
• Subjects: Genomics -- Periodicals; Bioinformatics -- Periodicals; 572.8
• DOI: 10.1093/nargab/lqac081
• Languages: English
• ISSNs: 2631-9268

Abstract

Abstract: 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 Tbg 1 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 Tbg 1-specific, of which three were shared by the 18 studied Tbg 1 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 Tbg 1. 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 Tbg 1 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 Tbg 1 populations, the latter ensuring the reliability of our novel diagnostic assay.