Chua Angela Patricia B, Galay Remil L, Tanaka Tetsuya, Yamazaki Wataru
Department of Veterinary Paraclinical Sciences, College of Veterinary Medicine, University of the Philippines Los Baños, College, Laguna, Los Baños 4031, Philippines.
Laboratory of Infectious Diseases, Joint Faculty of Veterinary Medicine, Kagoshima University, Korimoto 1-21-24, Kagoshima 890-0065, Japan.
Vet Sci. 2020 Oct 15;7(4):156. doi: 10.3390/vetsci7040156.
Canine monocytic ehrlichiosis caused by is one of the leading tick-borne diseases of dogs, particularly in tropical countries. A highly sensitive and specific diagnostic method is essential for early detection to facilitate treatment. This study was conducted to develop loop-mediated isothermal amplification (LAMP) assay, a highly sensitive yet simple molecular technique, targeting the citrate synthase () gene of . Canine blood samples were subjected to conventional PCR targeting . After analysis of the sequences of PCR amplicons, LAMP primers were generated. The optimum temperature and time for the LAMP assay were determined using eight samples-after which, the effectiveness and reproducibility of LAMP were verified by testing 40 samples, which included PCR-positive and negative samples. The detection limit was also established. The optimal condition for the assay was 61 °C for 60 min. Compared to PCR, the LAMP assay had a relative sensitivity and specificity of 92.5 and 100%, respectively. Statistical analysis using McNemar's test showed that the LAMP assay has no significant difference with PCR. Therefore, the LAMP assay developed in this study may be used as an alternative to PCR in the detection of .
由[病原体名称未提及]引起的犬单核细胞埃立克体病是犬类主要的蜱传疾病之一,在热带国家尤为如此。一种高度灵敏且特异的诊断方法对于早期检测以促进治疗至关重要。本研究旨在开发一种环介导等温扩增(LAMP)检测方法,这是一种高度灵敏但操作简单的分子技术,靶向[病原体名称未提及]的柠檬酸合酶([基因名称未提及])基因。对犬血样进行针对[病原体名称未提及]的常规PCR检测。在分析PCR扩增子序列后,设计了LAMP引物。使用8个样本确定了LAMP检测的最佳温度和时间,之后,通过检测40个样本(包括PCR阳性和阴性样本)验证了LAMP的有效性和可重复性。还确定了检测限。该检测的最佳条件是61℃反应60分钟。与PCR相比,LAMP检测的相对灵敏度和特异性分别为92.5%和100%。使用McNemar检验的统计分析表明,LAMP检测与PCR无显著差异。因此,本研究开发的LAMP检测方法可作为PCR检测[病原体名称未提及]的替代方法。