Dhakal Medhavi, Gompo Tulsi Ram, Devkota Prakash, Kafle Sharmila Chapagain, Subedi Janak Raj, Gong Haiyan, Arima Hiroaki, Culleton Richard, Asada Masahito, Pandey Kishor
Central Department of Zoology, Institute of Science and Technology, Tribhuvan University, Kathmandu 44601, Nepal.
Central Veterinary Laboratory, Kathmandu 44600, Nepal.
Pathogens. 2023 Aug 15;12(8):1045. doi: 10.3390/pathogens12081045.
Tick-borne protozoan parasites (TBPPs) cause significant problems for domestic animals' health in Nepal. TBPPs are routinely diagnosed by labor-intensive blood smear microscopy. In Nepal, there are some reports of and in cattle, although species identification is rarely performed. Therefore, we performed conventional nested PCR (nPCR) followed by sequence analysis to identify TBPP species infecting cattle in Nepal.
One hundred and six blood samples were collected from cattle in the Kathmandu Valley. Thin blood smears were prepared for microscopic examination. Parasite DNA was extracted from the blood, and nPCR and sequencing were performed to identify the TBPPs present.
Among the 106 samples, 45 (42.5%) were positive for piroplasm ( spp. and spp.) via microscope observation and 56 (52.8%) samples were positive via nPCR. The obtained PCR products were used for direct sequencing, and we identified the species as , , and . Phylogenetic analyses showed that the , and sequences from this study belonged to each species clade. On the other hand, was divided into two clades in the analysis, and our sequences were also divided in these two clades. The piroplasm-positive cattle showed lower hemoglobin and red blood cells than healthy cattle.
To the best of our knowledge, this study is the first to apply molecular detection and species determination of TBPPs in cattle in Nepal. The results of this study may be used as a starting point for the development of successful TBPP surveillance and prevention programs in Nepal.
蜱传播的原生动物寄生虫(TBPPs)给尼泊尔家畜的健康带来了重大问题。TBPPs通常通过劳动强度大的血涂片显微镜检查来诊断。在尼泊尔,有一些关于牛感染 和 的报道,不过很少进行物种鉴定。因此,我们进行了常规巢式PCR(nPCR),随后进行序列分析,以鉴定感染尼泊尔牛的TBPPs物种。
从加德满都谷地的牛身上采集了106份血样。制备薄血涂片用于显微镜检查。从血液中提取寄生虫DNA,并进行nPCR和测序以鉴定存在的TBPPs。
在106份样本中,通过显微镜观察,45份(42.5%)的梨形虫( 属和 属)呈阳性,通过nPCR,56份(52.8%)样本呈阳性。将获得的PCR产物用于直接测序,我们鉴定出的物种为 、 、 和 。系统发育分析表明,本研究中的 、 和 序列属于每个物种分支。另一方面, 在分析中被分为两个分支,我们的 序列也被分为这两个分支。梨形虫阳性的牛的血红蛋白和红细胞水平低于健康牛。
据我们所知,本研究首次在尼泊尔的牛中应用分子检测和TBPPs物种鉴定。本研究结果可作为尼泊尔成功开展TBPP监测和预防计划的起点。