“…The analytic sensitivity of the real-time quadriplex PCR assay was determined using 10-fold serial dilutions of purified TPpertenue genomic DNA (CDC-1 strain). The analytical specificity of the PCR assay was verified using DNA purified from 10 laboratory strains of TP-pallidum 8,9 (Nichols, SS 14, Mexico A, JV1, DAL-1, Madras, 1 strain from Maryland, 3 strains from Minnesota) and 11 clinical strains from South Africa, 11 13 laboratory strains of TP-pertenue 8,9 (CDC-1, CDC-2, CDC-2575, Samoa D, Samoa F, Ghana 051, Gauthier, and 6 strains from Indonesia), a clinical strain from Democratic Republic of the Congo, 6 and 2 strains of TP-endemicum (Bosnia A and Iraq B). In addition, a previously used panel of nonpathogenic treponemes (T. denticola, T. refringens, and T. phagedenis) and other microorganisms was included to determine the specificity of the assay.…”