Visceral leishmaniasis, a vector-borne disease caused by Leishmania donovani and Leishmania infantum, currently affects 12 million individuals in 88 countries. In the present study, a real-time PCR (rt-PCR) assay has been optimized and validated against 2 other routine methods, i.e., microscopy and limiting dilution culture assay, to estimate parasite load in the liver of infected Syrian hamsters (Mesocricetus auratus). A set of specific primers amplified a 116-bp target template of the kinetoplastid DNA of L. donovani in a SYBR® Green-based rt-PCR assay. To assess the methods, we tested 2 anti-leishmanial compounds belonging to the class of arylimidamides, DB745 (2,5-bis[2-ethoxy-4-(2-pyridylimino)aminophenyl]furan) and DB766 (2,5-bis[2-(2-propoxy)-4-(2-pyridylimino)aminophenyl]furan) for efficacy in vivo in Syrian hamsters infected with L. donovani promastigotes. Parasite load was quantified in liver by all 3 methods and was found comparable. Of the 3 methods, rt-PCR was the fastest and most convenient, sensitive, and reproducible method.
How to translate text using browser tools
1 February 2013
Real-Time PCR to Quantify Leishmania donovani in Hamsters
Anuradha Srivastava,
J. Mark Sweat,
Azliyati Azizan,
Brian Vesely,
Dennis E. Kyle
ACCESS THE FULL ARTICLE
Journal of Parasitology
Vol. 99 • No. 1
February 2013
Vol. 99 • No. 1
February 2013