A FRET-based real-time PCR assay to identify the main causal agents of New World tegumentary leishmaniasis

• Published in: PLoS neglected tropical diseases Vol. 7; no. 1; p. e1956
• Main Authors: Tsukayama, Pablo, Núñez, Jorge H, De Los Santos, Maxy, Soberón, Valeria, Lucas, Carmen M, Matlashewski, Greg, Llanos-Cuentas, Alejandro, Ore, Marianela, Baldeviano, G Christian, Edgel, Kimberly A, Lescano, Andres G, Graf, Paul C F, Bacon, David J
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 01-01-2013; Public Library of Science (PLoS)
• Subjects: Assaying; Biology; Care and treatment; Diagnosis; DNA, Kinetoplast - genetics; DNA, Protozoan - genetics; Endemic species; Enzymes; Etiology; Genetic aspects; Humans; Identification; Infections; Laboratories; Leishmania - classification; Leishmania - genetics; Leishmania - isolation & purification; Leishmaniasis; Leishmaniasis, Cutaneous - diagnosis; Leishmaniasis, Cutaneous - parasitology; Medicine; Molecular Diagnostic Techniques - methods; Parasites; Parasitic diseases; Parasitology - methods; Peru; Polymerase chain reaction; Protozoa; Real-Time Polymerase Chain Reaction - methods; Sensitivity and Specificity; Surveillance; Time Factors; Tropical diseases; Vector-borne diseases; Peru; South America; United States > US; DNA, Kinetoplast; Molecular Diagnostic Techniques; Parasitology; Leishmaniasis, Cutaneous; Time Factors; Sensitivity & Specificity; Humans; Leishmania; Peru; Real-Time Polymerase Chain Reaction; DNA, Protozoan
• ISSN: 1935-2735; 1935-2727; 1935-2735
• DOI: 10.1371/journal.pntd.0001956

In South America, various species of Leishmania are endemic and cause New World tegumentary leishmaniasis (NWTL). The correct identification of these species is critical for adequate clinical management and surveillance activities. We developed a real-time polymerase chain reaction (PCR) assay and evaluated its diagnostic performance using 64 archived parasite isolates and 192 prospectively identified samples collected from individuals with suspected leishmaniasis enrolled at two reference clinics in Lima, Peru. The real-time PCR assay was able to detect a single parasite and provided unambiguous melting peaks for five Leishmania species of the Viannia subgenus that are highly prevalent in South America: L. (V.) braziliensis, L. (V.) panamensis, L. (V.) guyanensis, L. (V.) peruviana and L. (V.) lainsoni. Using kinetoplastid DNA-based PCR as a gold standard, the real-time PCR had sensitivity and specificity values of 92% and 77%, respectively, which were significantly higher than those of conventional tests such as microscopy, culture and the leishmanin skin test (LST). In addition, the real-time PCR identified 147 different clinical samples at the species level, providing an overall agreement of 100% when compared to multilocus sequence typing (MLST) data performed on a subset of these samples. Furthermore, the real-time PCR was three times faster and five times less expensive when compared to PCR - MLST for species identification from clinical specimens. In summary, this new assay represents a cost-effective and reliable alternative for the identification of the main species causing NWTL in South America.