Login / Signup

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

Manon GeertsZihao ChenNicolas BebronneNicholas J SavillAchim SchnauferPhilippe BüscherNick Van ReetFrederik Van den Broeck
Published in: NAR genomics and bioinformatics (2022)
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.
Keyphrases