A Single-Nucleotide-Polymorphism Real-Time PCR Assay for Genotyping of Mycobacterium tuberculosis complex in Peri-Urban Kampala
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Date
2015-09
Journal Title
Journal ISSN
Volume Title
Publisher
BMC Infectious Diseases
Abstract
Background: Accurate and high-throughput genotyping of Mycobacterium tuberculosis complex (MTBC) may be
important for understanding the epidemiology and pathogenesis of tuberculosis (TB). In this study, we report the development of a LightCycler® real-time PCR single-nucleotide-polymorphism (LRPS) assay for the rapid
determination of MTBC lineages/sublineages in minimally processed sputum samples from TB patients.
Method: Genotyping analysis of 70 MTBC strains was performed using the Long Sequence Polymorphism-PCR
(LSP-PCR) technique and the LRPS assay in parallel. For targeted sequencing, 9 MTBC isolates (three isolates per
MTBC lineage) were analyzed for lineage-specific single nucleotide polymorphisms (SNPs) in the following three
genes to verify LRPS results: Rv004c for MTB Uganda family, Rv2962 for MTB lineage 4, and Rv0129c for MTB lineage3. The MTBC lineages present in 300 smear-positive sputum samples were then determined by the validated LRPS method without prior culturing.
Results: The LSP-PCR and LRPS assays produced consistent genotyping data for all 70 MTBC strains; however, the LSP-PCR assay was 10-fold less sensitive than the LRPS method and required higher DNA concentrations to
successfully characterize the MTBC lineage of certain samples. Targeted sequencing of genes containing lineage specific SNPs was 100 % concordant with the genotyping results and provided further validation of the LRPS assay. Of the 300 sputum samples analyzed, 58 % contained MTBC from the MTBC-Uganda family, 27 % from the MTBC lineage 4 (excluding MTBC Uganda family), 13 % from the MTBC lineage 3, and the remaining 2 % were of indeterminate lineage.
Conclusion: The LRPS assay is a sensitive, high-throughput technique with potential application to routine
genotyping of MTBC in sputum samples from TB patients
Description
The study, we report the development of a LightCycler® real-time PCR single-nucleotide-polymorphism (LRPS) assay for the rapid determination of MTBC lineages/sublineages in minimally processed sputum samples from TB patients.
Keywords
Single nucleotide polymorphism, Lineages, Long sequence polymorphism, High-throughput
Citation
Wampande, Eddie M., Hatzios, Stavroula K., Achan, Beatrice, Mupere, Ezekiel, Nsereko, Mary, Mayanja, Harriet K., Eisenach, Kathleen, Boom, W Henry, Gagneux, Sebastien, Joloba, Moses L., 2015. A single-nucleotide-polymorphism real-time PCR assay for genotyping of Mycobacterium tuberculosis complex in peri-urban Kampala.