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. 2017 Mar;96(3):656-659.
doi: 10.4269/ajtmh.16-0811. Epub 2017 Apr 6.

Susceptibility to Miltefosine in Brazilian Clinical Isolates of Leishmania (Viannia) braziliensis

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Susceptibility to Miltefosine in Brazilian Clinical Isolates of Leishmania (Viannia) braziliensis

Caroline R Espada et al. Am J Trop Med Hyg. 2017 Mar.

Abstract

Leishmania (Viannia) braziliensis is the main causative species of tegumentary leishmaniasis in Brazil. In this study, we evaluated the susceptibility of 16 clinical isolates of L. (V.) braziliensis from different regions of Brazil to miltefosine in vitro. Half-maximal inhibitory concentrations of miltefosine varied from 22.9 to 144.2 μM against promastigotes and from 0.3 to 4.2 μM against intracellular amastigotes. No significant differences were found between isolates of different geographical origins. A clear correlation between the EC50 against promastigotes and amastigotes within each isolate was found. These findings contribute to the evaluation of miltefosine's potential and limitations for the treatment of tegumentary leishmaniasis in Brazil.

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Figures

Figure 1.
Figure 1.
Susceptibility of promastigotes and intracellular amastigotes of Leishmania (V.) braziliensis isolates to miltefosine. (A) EC50 determined against promastigotes. (B) EC50 determined against intracellular amastigotes. “T” indicates the type strains M2903 and H3227, “GO” isolates from Goiás, and “BA” isolates from Bahia. (C) Comparison between the EC50 against promastigotes and amastigotes. The box indicates the 25th–75th percentiles. The line in the middle of the box indicates the median; * P < 0.0001 (Mann–Whitney test). (D) Correlation between the EC50 determined against promastigotes and amastigotes for each clinical isolate. Spearman coefficient r = 0.793; P = 0.008.

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