School of Life Sciences, University of Technology Sydney, Ultimo, Australia.
Department of Microbiology, St. Vincent's Hospital Sydney, Darlinghurst, Australia.
Am J Trop Med Hyg. 2019 Sep;101(3):590-601. doi: 10.4269/ajtmh.19-0095.
Leishmaniasis is a vector-borne disease caused by protozoan parasites of the genus. In Australia, leishmaniasis is an imported disease that is presenting itself at increased rates because of international travel, the influx of immigrants, and deployment of military operations to endemic regions. Although species are morphologically indistinguishable, there is a strong correlation between some causative species of leishmaniasis and the subsequent response to the treatments available and patient outcome. Consequently, identification of the infective species is imperative as misidentification can result in the administering of an ineffective drug. The aim of this study was to develop a simple diagnostic tool with high sensitivity and specificity, which is capable of detecting the presence of the parasite and accurately differentiating the causative species in question. Using the advantageous properties of the maxi-circle kinetoplast DNA, a polymerase chain reaction (PCR)-restriction fragment length polymorphism (RFLP) targeting the gene was developed for the analysis of imported cases of human leishmaniasis in Australia. Designed as a dual analysis, concurrent PCR of maxi-circle DNA and digestion with two separate enzymes (III and CH4IV), this study provides an appraisal on 24 imported cases of leishmaniasis between 2008 and 2017. Five species were reported, with members of the subgenus being the most common. The implementation of novel diagnostic procedures for leishmaniasis such as the one reported here is needed to establish a gold standard practice for the diagnosis and treatment of leishmaniasis.
利什曼病是一种由原生动物寄生虫引起的虫媒病。在澳大利亚,利什曼病是一种输入性疾病,由于国际旅行、移民涌入和军事行动部署到流行地区,其发病率不断上升。尽管 种在形态上无法区分,但某些利什曼病的致病种与随后对现有治疗方法的反应和患者的预后之间存在很强的相关性。因此,确定感染物种至关重要,因为错误识别可能导致使用无效药物。本研究旨在开发一种具有高灵敏度和特异性的简单诊断工具,能够检测寄生虫的存在,并准确区分有关的致病种。利用 maxi-circle 动基体 DNA 的有利特性,针对 基因开发了一种聚合酶链反应(PCR)-限制性片段长度多态性(RFLP),用于分析澳大利亚输入性人类利什曼病病例。该研究设计为双重分析,同时对 maxi-circle DNA 进行 PCR 扩增,并使用两种单独的酶(III 和 CH4IV)进行消化,对 2008 年至 2017 年间的 24 例输入性利什曼病病例进行了评估。报告了 5 种 种,其中亚属成员最为常见。需要实施利什曼病的新诊断程序,如这里报告的那样,以建立利什曼病诊断和治疗的金标准实践。