4.6 Article

Single nucleotide polymorphisms and copy-number variations in the Trypanosoma brucei repeat (TBR) sequence can be used to enhance amplification and genotyping of Trypanozoon strains

Journal

PLOS ONE
Volume 16, Issue 10, Pages -

Publisher

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0258711

Keywords

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Funding

  1. Bill and Melinda Gates foundation [OPP1174221]
  2. grant CHARHAT-RDC from the Departement Economie, Wetenschap & Innovatie (EWI-Vlaanderen.be)
  3. Fonds Wetenschappelijk Onderzoek (fwo.be) [1.5.093.16N]
  4. Bill and Melinda Gates Foundation [OPP1174221] Funding Source: Bill and Melinda Gates Foundation

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The TBR sequence in Trypanosoma brucei is not as homogenous as previously believed, with various sequences of different lengths and key single nucleotide polymorphisms. The qTBR PCR developed in this study enhances amplification and genotyping of all Trypanozoon strains, making it a promising tool for prevalence studies of African trypanosomiasis.
The Trypanosoma brucei repeat (TBR) is a tandem repeat sequence present on the Trypanozoon minichromosomes. Here, we report that the TBR sequence is not as homogenous as previously believed. BLAST analysis of the available T. brucei genomes reveals various TBR sequences of 177 bp and 176 bp in length, which can be sorted into two TBR groups based on a few key single nucleotide polymorphisms. Conventional and quantitative PCR with primers matched to consensus sequences that target either TBR group show substantial copy-number variations in the TBR repertoire within a collection of 77 Trypanozoon strains. We developed the qTBR, a novel PCR consisting of three primers and two probes, to simultaneously amplify target sequences from each of the two TBR groups into one single qPCR reaction. This dual probe setup offers increased analytical sensitivity for the molecular detection of all Trypanozoon taxa, in particular for T.b. gambiense and T. evansi, when compared to existing TBR PCRs. By combining the qTBR with 18S rDNA amplification as an internal standard, the relative copy-number of each TBR target sequence can be calculated and plotted, allowing for further classification of strains into TBR genotypes associated with East, West or Central Africa. Thus, the qTBR takes advantage of the single-nucleotide polymorphisms and copy number variations in the TBR sequences to enhance amplification and genotyping of all Trypanozoon strains, making it a promising tool for prevalence studies of African trypanosomiasis in both humans and animals.

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