Rajasekariah G-Halli R, Cardoso Luis, Dogcio Diane A, Martin Samuel K, Smithyman Anthony M
Cellabs Pty Ltd, 7/27 Dale St, Brookvale, NSW, 2100 Australia.
Am J Trop Med Hyg. 2008 Apr;78(4):616-23.
Dogs which are infected with leishmania parasites serve as major reservoir hosts for zoonotic visceral leishmaniasis. The incidence of zoonotic visceral leishmaniasis is rising in many countries. This may be associated with the continuing drift of people and their pets from rural areas into peri-urban settings, particularly at the fringe of large cities. At the same time, there is evidence of adaptation of sand fly vectors to these urban settings. This has created an alarming situation because, even though domestic and stray dogs may be infected, many remain asymptomatic but are still highly infectious to the sand fly vectors and thus pose a serious threat to human health. Over half of the infected dogs have asymptomatic infections and current assays are not sensitive enough under field conditions to distinguish asymptomatic from symptomatic dogs. There is an urgent need for a specific and sensitive screening tool for use in the field. We have previously demonstrated that promastigote exo-antigen-based ELISAs can be used in the specific diagnosis of human visceral leishmaniasis (HVL). A cocktail of exo-antigens prepared from three species (L. infantum, L. donovani, and L. major) was used to develop and optimize a canine ELISA assay. Serum samples from dogs with a variety of pathological conditions but living in a non-leishmania endemic area were used as negative controls and their reactivity was used to determine a cut-off value for the ELISA. Samples from dogs residing in a leishmania endemic area were tested in parallel using direct agglutination (DAT), immunofluorescence (IFAT), and ELISA. The ELISA results correlated closely (100%) with the clinical symptoms, and were elevated in one asymptomatic dog. This sample was also found to be positive by IFAT. Based on its sensitivity and specificity, the cocktail exo-antigen-based ELISA may prove useful, even at 1:2,000 serum dilutions, for screening dogs in different geographical regions of the world.
感染利什曼原虫寄生虫的狗是动物源性内脏利什曼病的主要储存宿主。在许多国家,动物源性内脏利什曼病的发病率正在上升。这可能与人和他们的宠物持续从农村地区向城市周边地区迁移有关,特别是在大城市的边缘地带。与此同时,有证据表明白蛉媒介已适应这些城市环境。这造成了一种令人担忧的局面,因为尽管家养犬和流浪犬可能被感染,但许多犬仍无症状,但对白蛉媒介仍具有高度传染性,从而对人类健康构成严重威胁。超过一半的感染犬有无症状感染,而目前的检测方法在野外条件下不够灵敏,无法区分无症状犬和有症状犬。迫切需要一种用于野外的特异性和灵敏的筛查工具。我们之前已经证明,基于前鞭毛体外抗原的酶联免疫吸附测定(ELISA)可用于人类内脏利什曼病(HVL)的特异性诊断。用从三种利什曼原虫(婴儿利什曼原虫、杜氏利什曼原虫和硕大利什曼原虫)制备的外抗原混合物来开发和优化犬ELISA检测方法。将来自生活在非利什曼病流行区、患有各种病理状况的犬的血清样本用作阴性对照,并利用其反应性来确定ELISA的临界值。对来自利什曼病流行区的犬的样本同时使用直接凝集试验(DAT)、免疫荧光试验(IFAT)和ELISA进行检测。ELISA结果与临床症状密切相关(100%),并且在一只无症状犬中结果升高。该样本经IFAT检测也呈阳性。基于其敏感性和特异性,基于外抗原混合物的ELISA可能被证明是有用的,即使在血清稀释度为1:2000时,也可用于筛查世界不同地理区域的犬。