REAL-TIME PCR TO QUANTIFY LEISHMANIA DONOVANI IN HAMSTERS

被引:17
|
作者
Srivastava, Anuradha [1 ]
Sweat, J. Mark [1 ]
Azizan, Azliyati [1 ]
Vesely, Brian [1 ]
Kyle, Dennis E. [1 ]
机构
[1] Univ S Florida, Dept Global Hlth, Tampa, FL 33612 USA
关键词
POLYMERASE-CHAIN-REACTION; VISCERAL LEISHMANIASIS; PERIPHERAL-BLOOD; IMMUNE-RESPONSE; BALB/C MICE; INFANTUM; INFECTION; QUANTIFICATION; IDENTIFICATION; DIAGNOSIS;
D O I
10.1645/GE-3221.1
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
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 (R) 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.
引用
收藏
页码:145 / 150
页数:6
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