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. 2017 Jan 25;55(2):526–534. doi: 10.1128/JCM.01954-16

FIG 1.

FIG 1

(A) Linear amplification graph for the TaqMan-based assay. Leishmania (Viannia) braziliensis culture (pink arrow) (CT = 18.62), Leishmania (Viannia) guyanensis culture (black arrow) (CT = 31.86), Trypanosoma cruzi culture (brown arrow) (CT = 34.09). Leishmania amazonensis, DNA from healthy human skin, and a nontemplate control remained under the threshold line (red arrow) (CT = 0). y axis, normalized fluorescence; x axis, number of cycles. (B) Linear amplification graph for the SYBR Green-based assay. Leishmania (Viannia) braziliensis culture (green arrow) (CT = 10.84), Leishmania (Viannia) guyanensis culture (pink arrow) (CT = 25.13), and Trypanosoma cruzi culture (black arrow) (CT = 30.05). Leishmania amazonensis, DNA from healthy human skin and a nontemplate control remained under the threshold line (red arrow) (CT = 0). y axis, normalized fluorescence; x axis, number of cycles. (C) Melting curve for the SYBR Green-based assay. Expected melting curve analysis for Leishmania (Viannia) braziliensis culture (blue arrow). y axis, normalized fluorescence; x axis, temperature (°C). The images' scales were adjusted to fit the images in the panels.