Department of Parasitology, U.S. Naval Medical Research Unit No. 6 (NAMRU-6), Lima, Peru.
PLoS Negl Trop Dis. 2013;7(1):e1956. doi: 10.1371/journal.pntd.0001956. Epub 2013 Jan 3.
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.
在南美洲,各种利什曼原虫物种是地方性的,并导致新世界皮肤利什曼病(NWTL)。正确识别这些物种对于充分的临床管理和监测活动至关重要。我们开发了一种实时聚合酶链反应(PCR)检测方法,并使用 64 个存档寄生虫分离物和 192 个从秘鲁利马的两个参考诊所招募的疑似利什曼病患者中前瞻性鉴定的样本评估了其诊断性能。实时 PCR 检测方法能够检测到单个寄生虫,并为在南美洲高度流行的五种 Viannia 亚属利什曼原虫提供明确的熔解峰:L.(V.)braziliensis、L.(V.)panamensis、L.(V.)guyanensis、L.(V.)peruviana 和 L.(V.)lainsoni。使用动基体 DNA 为基础的 PCR 作为金标准,实时 PCR 的敏感性和特异性值分别为 92%和 77%,明显高于显微镜检查、培养和利什曼原虫皮肤试验(LST)等常规检测方法。此外,与对这些样本的一部分进行的多位点序列分型(MLST)数据相比,实时 PCR 在物种水平上鉴定了 147 种不同的临床样本,总体一致性为 100%。此外,与 PCR-MLST 相比,实时 PCR 用于从临床标本中鉴定物种的速度快三倍,成本低五倍。总之,这种新的检测方法代表了一种具有成本效益和可靠的替代方法,可用于鉴定导致南美洲 NWTL 的主要物种。