A real-time PCR assay for quantification of parasite burden in murine models of leishmaniasis.

Journal Article (Journal Article)

Eukaryotic parasites in the genus Leishmania place approximately 350 million people per year at risk of disease. In addition to their global health significance, Leishmania spp. have served as an important model for delineating basic concepts in immunology such as T-helper cell polarization. There have been many qPCR-based assays reported for measuring parasite burden in humans and animals. However, these are largely optimized for use in clinical diagnosis and not specifically for animal models. This has led several of these assays to have suboptimal characteristics for use in animal models. For example, multi-copy number genes have been frequently used to increase sensitivity but are subject to greater plasticity within the genome and thus may confound effects of experimental manipulations in animal models. In this study, we developed a sybr-green based quantitative touchdown PCR assay for a highly conserved and single-copy putative RNA-binding protein, DRBD3. With primers that share greater than 90% sequence identity across all sequenced Leishmania spp., we demonstrate that this assay has a lower limit of detection of 100 fg of parasite DNA for Leishmania major, L. donovani, L. venezuelensis, and L. panamensis. Using C57BL6/J mice, we used this assay to monitor parasite burden over 1 month of infection with two strains of L. major (Seidman and Friedlin), and L. venezeuelensis. These characteristics rival the sensitivity of previously reported qPCR based methods of parasite quantitation while amplifying a stable, single copy gene. Use of this protocol in the future will lead to improved accuracy in animal based models and help to tease apart differences in biology of host-parasite interactions.

Full Text

Duke Authors

Cited Authors

  • Antonia, AL; Wang, L; Ko, DC

Published Date

  • 2018

Published In

Volume / Issue

  • 6 /

Start / End Page

  • e5905 -

PubMed ID

  • 30430041

Pubmed Central ID

  • PMC6231426

International Standard Serial Number (ISSN)

  • 2167-8359

Digital Object Identifier (DOI)

  • 10.7717/peerj.5905


  • eng

Conference Location

  • United States