Tong Qunbo, Chen Rui, Kong Qingming, Goossens Julie, Radwanska Magdalena, Lou Di, Ding Jianzu, Zheng Bin, Fu Yixiu, Wang Tianping, Stefan Magez, Lu Shaohong
Department of Immunity and Biochemistry, Institute of Parasitic Disease, Zhejiang Academy of Medical Sciences, Hangzhou, China.
Laboratory of Cellular and Molecular Immunology, Vrije Universiteit Brussel, Brussels, Belgium.
Vet Parasitol. 2018 Jan 30;250:1-6. doi: 10.1016/j.vetpar.2017.12.006. Epub 2017 Dec 6.
Trypanosoma evansi (T. evansi) is the most widely spread pathogenic trypanosome in the world. The control of trypanosomiasis depends on accurate diagnosis and effective treatment. Focusing on the presence of T. evansi in Asia, we developed a detection assay based on tracing phosphate ions (Pi) generated during LAMP targeting the variant surface glycoprotein (VSG) gene of Rode Trypanozoon antigenic type 1.2 (RoTat 1.2 VSG). The diagnostic potential as well as the use of the assay as a test-of-cure method after berenil treatment, was assessed in mice at different time points of infection. In addition, 67 buffalo blood collected from Tongling county, Anhui province, as well as 42 cattle sera from the Shanghai area, were used to evaluate the diagnostic validity of the test. The detection limit of the novel LAMP assay was determined to be as low as 1 fg of T. evansi DNA, while the reaction time for the test was only 30min. Hence it outperforms both microscopy and PCR. In the test-of-cure assessment, successful berenil mediated cure could be confirmed within 48h after treatment. This offers a tremendous advantage over conventional antibody-based diagnostic tools in which successful cure only can be confirmed after months. In the cattle and buffalo screening, the LAMP was able to detect a false-negative determined sample, wrongly classified in a conventional microscopy and PCR screening. Finally, no cross-reactivity was observed with other zoonotic parasites, such as T. evansi type B, T. congolense, T. brucei, Schistosoma japonicum, Plasmodium falciparum, Leishmania donovani, Toxoplasma gondii and Angiostrongylus cantonensis. We conclude that the novel LAMP assay is sensitive, specific and convenient for field use, particularly in areas where infection incidence has become extremely low. The LAMP assay could be used as a tool for trypanosomiasis control and elimination strategies in areas where T. evansi Type A infections are causing a threat to livestock farming.
伊氏锥虫(T. evansi)是世界上传播最广泛的致病性锥虫。锥虫病的控制依赖于准确的诊断和有效的治疗。针对伊氏锥虫在亚洲的存在情况,我们开发了一种检测方法,该方法基于追踪环介导等温扩增(LAMP)过程中产生的磷酸根离子(Pi),LAMP靶向罗德锥虫抗原型1.2(RoTat 1.2)的可变表面糖蛋白(VSG)基因。在小鼠感染的不同时间点评估了该检测方法的诊断潜力以及作为贝尼尔治疗后治愈检测方法的用途。此外,还使用了从安徽省铜陵县采集的67份水牛血液以及上海地区的42份牛血清来评估该检测方法的诊断有效性。新型LAMP检测方法的检测限低至1 fg伊氏锥虫DNA,而检测反应时间仅为30分钟。因此,它优于显微镜检查和聚合酶链反应(PCR)。在治愈检测评估中,治疗后48小时内即可确认贝尼尔介导的治愈成功。这与传统的基于抗体的诊断工具相比具有巨大优势,传统工具只有在数月后才能确认治愈成功。在牛和水牛的筛查中,LAMP能够检测出在传统显微镜检查和PCR筛查中被错误分类的假阴性样本。最后,未观察到与其他人畜共患寄生虫的交叉反应,如B型伊氏锥虫、刚果锥虫、布氏锥虫、日本血吸虫、恶性疟原虫、杜氏利什曼原虫、刚地弓形虫和广州管圆线虫。我们得出结论,新型LAMP检测方法灵敏、特异且便于现场使用,特别是在感染发病率已极低的地区。LAMP检测方法可作为伊氏锥虫A型感染对畜牧业造成威胁的地区锥虫病控制和消除策略的工具。