Suganuma Keisuke, Narantsatsral Sandagdorj, Battur Banzragch, Yamasaki Shino, Otgonsuren Davaajav, Musinguzi Simon Peter, Davaasuren Batdorj, Battsetseg Badgar, Inoue Noboru
National Research Center for Protozoan Diseases, OIE Reference Laboratory for Surra, Obihiro University of Agriculture and Veterinary Medicine, Inada, Obihiro, Hokkaido, 080-8555, Japan.
Institute of Veterinary Medicine, Laboratory of Molecular Genetics, Mongolian University of Life Sciences, Zaisan, 17024, Ulaanbaatar, Mongolia.
Parasit Vectors. 2016 Aug 31;9(1):481. doi: 10.1186/s13071-016-1755-3.
Trypanosoma equiperdum causes dourine via sexual transmission in Equidae. T. equiperdum is classified under the subgenus Trypanozoon along with the T. brucei sspp. and T. evansi; however, the species classification of Trypanozoon remains a controversial topic due to the limited number of T. equiperdum reference strains. In addition, it is possible that some were misclassified T. evansi strains. Thus, there is a strong need for a new T. equiperdum strain directly isolated from the genital mucosa of a horse with a clinically- and parasitologically-confirmed dourine infection.
Trypanosomes isolated from the urethral tract of a stallion with suspected dourine, were directly cultivated using soft agarose media at 37 °C in 5 % CO2. For molecular characterization, 18S ribosomal RNA (rRNA) gene, the internal transcribed spacer (ITS) and 8 maxicircle DNA regions were amplified by a PCR and their sequences were determined. To analyze the ratio of the kinetoplastic/akinetoplastic population, the kinetoplasts and the nuclei of trypanosomes were subjected to Hoechst staining and observed by fluorescence microscopy.
In addition to the clinical symptoms and the molecular diagnosis, this stallion was definitively diagnosed with dourine by the detection of trypanosomes in the urethral mucosa. These results strongly suggested that the isolated trypanosome was true T. equiperdum. T. equiperdum isolated from the urethral tract was adapted in vitro using soft agarose media. Based on the results of a phylogenetic analysis of 18S rRNA and ITS, this T. equiperdum isolate was classified into the Trypanozoon clade. In a PCR of the maxicircle DNA region, only NADH-dehydrogenase subunits 4 and 5 was amplified. Clear kinetoplasts were observed in most of the T. equiperdum isolates. In contrast, most culture-adapted T. equiperdum were of the akinetoplastic form.
We concluded that our isolated trypanosome was the first confirmed case of T. equiperdum in Mongolia and named it "T. equiperdum IVM-t1". T. equiperdum IVM-t1 was well adapted and propagated in soft agarose media, which indicates that this culture method is useful for isolation of T. equiperdum from horses with dourine.
马媾疫锥虫通过马科动物的性传播引发马媾疫。马媾疫锥虫与布氏锥虫复合种及伊氏锥虫一同被归类于锥虫亚属;然而,由于马媾疫锥虫参考菌株数量有限,锥虫亚属的物种分类仍是一个有争议的话题。此外,有可能存在一些被误分类为伊氏锥虫的菌株。因此,迫切需要从一匹临床和寄生虫学确诊为马媾疫感染的马的生殖黏膜中直接分离出一株新的马媾疫锥虫菌株。
从一匹疑似感染马媾疫的种马尿道中分离出的锥虫,使用软琼脂糖培养基在37°C、5%二氧化碳条件下直接培养。为进行分子特征分析,通过聚合酶链反应(PCR)扩增18S核糖体RNA(rRNA)基因、内部转录间隔区(ITS)和8个大环DNA区域,并测定其序列。为分析动基体/无动基体群体的比例,对锥虫的动基体和细胞核进行Hoechst染色,并通过荧光显微镜观察。
除临床症状和分子诊断外,通过在尿道黏膜中检测到锥虫,这匹种马被明确诊断为马媾疫。这些结果强烈表明分离出的锥虫是真正的马媾疫锥虫。从尿道分离出的马媾疫锥虫在体外使用软琼脂糖培养基进行了适应性培养。基于18S rRNA和ITS的系统发育分析结果,该马媾疫锥虫分离株被归类于锥虫进化枝。在大环DNA区域的PCR中,仅扩增出烟酰胺腺嘌呤二核苷酸脱氢酶亚基4和5。在大多数马媾疫锥虫分离株中观察到清晰的动基体。相比之下,大多数适应培养的马媾疫锥虫为无动基体形式。
我们得出结论,我们分离出的锥虫是蒙古首例确诊的马媾疫锥虫病例,并将其命名为“马媾疫锥虫IVM - t1”。马媾疫锥虫IVM - t1在软琼脂糖培养基中适应性良好且能增殖,这表明这种培养方法对于从感染马媾疫的马中分离马媾疫锥虫很有用。