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. Author manuscript; available in PMC: 2021 Oct 28.
Published in final edited form as: Sci Transl Med. 2020 Oct 28;12(567):eabb7656. doi: 10.1126/scitranslmed.abb7656

Fig. 1. Effect of varying the frequency and dosage of BNZ administration on the control of T. cruzi infection in mice.

Fig. 1.

(A) Schematic of infection, treatment and footpad imaging. IFN-gamma deficient mice (5 mice in each group) were infected in the footpads with 105 trypomastigotes of the Luciferase-expressing Colombiana strain of T. cruzi and treated at indicated time points with either 100 or 500mg/kg oral BNZ. (B) Representative images showing footpad bioluminescent signal before and after treatment. The heat map is on a log10 scale and indicates the intensity of bioluminescence from low (blue) to high (red). (C) Parasite bioluminescence quantification following D-luciferin injection was measured at various times post-treatment in the footpads of mice infected and treated. Each data point represents the mean of 8 footpads bioluminescence from four mice expressed on a logarithmic scale. After subtraction of the background signal, the average radiance measurements (photons/second /cm2/sr) were quantified. Data are shown as mean ± standard error of the mean. (D) T. cruzi DNA determined by quantitative real time polymerase chain reaction in footpads of untreated or treated mice at 12 days post-infection (5 days post-treatment). C57BL/6 wild-type mice (10-12 mice in each group) were infected in the footpads with 103 trypomastigotes of the Brazil strain of T. cruzi and left untreated or treated at day 2 post-infection with a single dose of BNZ at 100 or 500mg/kg concentration. A statistically significant difference was set at p=0.05.