Rboxytetramethylrhodamine; MGBNFQ, minor groove binding nonfluorescent quencher. doi:10.1371/journal.pone.0052719.ta bReal-Time PCR Detection of Plasmodium in MosquitoResults Mosquito Collection and Plasmodium Infection rates by ELISA-CSPA total of 1.830 An. gambiae s.l. and 1.234 members of the An. funestus group were collected in the field and analyzed by ELISACSP. Fifty An. gambiae s.s. and twenty An. funestus mosquitoes were found positive to P. falciparum, corresponding to a prevalence of infection of 2.7 and 1.62 respectively. In this study, 200 hundred specimens (100 An. gambiae s.s. and 100 An. funestus) were used in the evaluation of the real-time PCR assays. For An. gambiae, 50 Plasmodium infected and 50 randomly selected uninfected mosquitoes were included according to ELISA-CSP. Due to lower prevalence of P. falciparum infection among An. funestus mosquitoes, only 20 infected mosquitoes and 80 randomly selected negative were included.Table 2. Specific detection of Plasmodium DNA by real-time PCR in the artificial target mixtures.Probe FAM Plasmids Pf.Probe VIC MAL 0 0 0 18.2 24.66 33.45 Plasmo 18.74 23.91 33.16 17.86 23.52 32.05 OVA 0 0 0 18.83 24.66 33.FAL 18.15 24.05 33.84 0 0Pf. 105 Pf. 102 (Po/Pm). 107 (Po/Pm). 105 (Po/Pm).Design and Validation of the Real-time PCR AssaysThe quality of the DNA extracted was checked by spectrophotometric analysis at 260 nm and 280 nm respectively, and the absence of PCR inhibitors in the preparation was confirmed by amplification of the ribosomal protein S7 in all samples; means Ct values were 24.7262.62 for An. gambiae and 24.8461.5 for An. funestus. As part of the study, we first evaluated each detection system on a 10-fold dilution range of the corresponding standard (from 1.100 to 1.1010 copies). However, the optimal linear range of the get 374913-63-0 external standard curves was observed from 1.101 to 1.1010 copies with PCR efficiencies all above 90 . Amplification of non-specific targets guided the combination of duplex assays. Evaluation of duplex Lixisenatide assays for the simultaneous detection of Plasmodium spp in the same reaction was performed in plasmid mixing experiments. Results presented in Table 2 and figure 1 highlight substantial specificity and a lack of competition between the mixed oligonucleotides.Footnote: Validation of real-time PCR on artificial mixed targets. Plasmids constructs are: Pf, Po and Pm for P. falciparum, P. ovale and P. malariae respectively. Corresponding detection systems primers/probe are shown as FAL, MAL, OVA and Plasmo. Data are cycle threshold (Ct) values. doi:10.1371/journal.pone.0052719.tfalciparum by Elisa-CSP, the presence of Plasmodium DNA was PCR-confirmed in 62 samples (8 samples were found negative by PCR). Among the 130 ELISA-CSP negative mosquito’s homogenates, the absence of Plasmodium was PCR-confirmed in 127 samples (3 samples were found positive by PCR). The real-time PCR method therefore showed relatively high values of sensitivity 88.6 (Se = 62/70*100) and specificity of 98 (Sp = 127/ 130*100) as compared to the ELISA-CSP here considered as the reference test. The agreement was “excellent” (k = 0.8 and P,0.05) between real-time PCR and ELISA-CSP.Prevalence and Co-infection Rates with Plasmodium spp in MosquitoesThe infection rates with Plasmodium spp are shown in Figure 2. The speciation by real-time PCR of the 43 PCR positive An. gambiae s.s. and 22 PCR positive An. funestus revealed the presence of P. falciparum in all samples (100 ). While mono.Rboxytetramethylrhodamine; MGBNFQ, minor groove binding nonfluorescent quencher. doi:10.1371/journal.pone.0052719.ta bReal-Time PCR Detection of Plasmodium in MosquitoResults Mosquito Collection and Plasmodium Infection rates by ELISA-CSPA total of 1.830 An. gambiae s.l. and 1.234 members of the An. funestus group were collected in the field and analyzed by ELISACSP. Fifty An. gambiae s.s. and twenty An. funestus mosquitoes were found positive to P. falciparum, corresponding to a prevalence of infection of 2.7 and 1.62 respectively. In this study, 200 hundred specimens (100 An. gambiae s.s. and 100 An. funestus) were used in the evaluation of the real-time PCR assays. For An. gambiae, 50 Plasmodium infected and 50 randomly selected uninfected mosquitoes were included according to ELISA-CSP. Due to lower prevalence of P. falciparum infection among An. funestus mosquitoes, only 20 infected mosquitoes and 80 randomly selected negative were included.Table 2. Specific detection of Plasmodium DNA by real-time PCR in the artificial target mixtures.Probe FAM Plasmids Pf.Probe VIC MAL 0 0 0 18.2 24.66 33.45 Plasmo 18.74 23.91 33.16 17.86 23.52 32.05 OVA 0 0 0 18.83 24.66 33.FAL 18.15 24.05 33.84 0 0Pf. 105 Pf. 102 (Po/Pm). 107 (Po/Pm). 105 (Po/Pm).Design and Validation of the Real-time PCR AssaysThe quality of the DNA extracted was checked by spectrophotometric analysis at 260 nm and 280 nm respectively, and the absence of PCR inhibitors in the preparation was confirmed by amplification of the ribosomal protein S7 in all samples; means Ct values were 24.7262.62 for An. gambiae and 24.8461.5 for An. funestus. As part of the study, we first evaluated each detection system on a 10-fold dilution range of the corresponding standard (from 1.100 to 1.1010 copies). However, the optimal linear range of the external standard curves was observed from 1.101 to 1.1010 copies with PCR efficiencies all above 90 . Amplification of non-specific targets guided the combination of duplex assays. Evaluation of duplex assays for the simultaneous detection of Plasmodium spp in the same reaction was performed in plasmid mixing experiments. Results presented in Table 2 and figure 1 highlight substantial specificity and a lack of competition between the mixed oligonucleotides.Footnote: Validation of real-time PCR on artificial mixed targets. Plasmids constructs are: Pf, Po and Pm for P. falciparum, P. ovale and P. malariae respectively. Corresponding detection systems primers/probe are shown as FAL, MAL, OVA and Plasmo. Data are cycle threshold (Ct) values. doi:10.1371/journal.pone.0052719.tfalciparum by Elisa-CSP, the presence of Plasmodium DNA was PCR-confirmed in 62 samples (8 samples were found negative by PCR). Among the 130 ELISA-CSP negative mosquito’s homogenates, the absence of Plasmodium was PCR-confirmed in 127 samples (3 samples were found positive by PCR). The real-time PCR method therefore showed relatively high values of sensitivity 88.6 (Se = 62/70*100) and specificity of 98 (Sp = 127/ 130*100) as compared to the ELISA-CSP here considered as the reference test. The agreement was “excellent” (k = 0.8 and P,0.05) between real-time PCR and ELISA-CSP.Prevalence and Co-infection Rates with Plasmodium spp in MosquitoesThe infection rates with Plasmodium spp are shown in Figure 2. The speciation by real-time PCR of the 43 PCR positive An. gambiae s.s. and 22 PCR positive An. funestus revealed the presence of P. falciparum in all samples (100 ). While mono.
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