Tumino Serena, Tolone Marco, Parco Alessio, Puleio Roberto, Arcoleo Giuseppe, Manno Claudia, Nicholas Robin A J, Loria Guido Ruggero
Dipartiment of Agricultural, Food and Environmental Science, University of Catania, 95123 Catania, Italy.
Istituto Zooprofilattico Sperimentale della Sicilia "A. Mirri", 90129 Palermo, Italy.
Animals (Basel). 2020 Mar 19;10(3):509. doi: 10.3390/ani10030509.
Contagious agalactia (CA), an infectious disease of small ruminants, caused by , is responsible for severe losses to dairy sheep production with substantial socioeconomic impacts on small-scale farmers. The diagnosis of CA is still problematic, time-consuming and requires well-equipped labs for confirmation of outbreaks. Therefore, rapid, accurate and cost-effective diagnostic tests are urgently needed. This work aims to validate a novel Loop-Mediated Isothermal Amplification (LAMP) test, based on the target gene, for the detection of in dairy sheep in order to confirm its potential practical use as a rapid and cheap field test. The LAMP system proposed in this study consists of a portable device composed of real-time fluorometer with the automatic interpretation of results displayed in a tablet. A total of 110 milk samples (90 positives and 20 negatives) were analysed to optimise the analysis procedure and to investigate the efficacy and robustness of the LAMP method. All samples were analysed using LAMP and conventional real-time PCR to compare the diagnostic sensitivity of the methods. The sensitivity of the LAMP was 10-fold higher than that of real-time PCR, with a detection limit up to 10 CFU/ml. The LAMP assay was able to detect in 81 of 90 (90%, 95%CI 0.84-0.96) positive milk samples compared to 69 (77%, 95%CI 0.59-0.95) positive samples detected by real-time PCR; no positive signal occurred for any of the negative milk samples in either test. Therefore, the LAMP assay was found to be more sensitive than real-time PCR, low-cost, easy to perform, fast and not affected by contamination, indicating its potential as an effective diagnostic tool in the field level for the diagnosis of CA.
传染性无乳症(CA)是一种小反刍动物的传染病,由……引起,给奶羊生产造成严重损失,对小规模养殖户产生重大社会经济影响。CA的诊断仍然存在问题,耗时且需要设备精良的实验室来确认疫情爆发。因此,迫切需要快速、准确且经济高效的诊断测试。这项工作旨在验证一种基于……靶基因的新型环介导等温扩增(LAMP)测试,用于检测奶羊中的……,以确认其作为一种快速且廉价的现场测试的潜在实际用途。本研究提出的LAMP系统由一个便携式设备组成,该设备包括一个实时荧光计,并能在平板电脑上自动显示结果解读。共分析了110份牛奶样本(90份阳性和20份阴性),以优化分析程序并研究LAMP方法的有效性和稳健性。所有样本均使用LAMP和传统实时PCR进行分析,以比较这些方法的诊断敏感性。LAMP的敏感性比实时PCR高10倍,检测限高达10 CFU/ml。与实时PCR检测到的69份(77%,95%CI 0.59 - 0.95)阳性样本相比,LAMP检测能够在90份阳性牛奶样本中的81份(90%,95%CI 0.84 - 0.96)中检测到……;在任何一项测试中,阴性牛奶样本均未出现阳性信号。因此,发现LAMP检测比实时PCR更敏感、成本低、易于操作、快速且不受污染影响,表明其作为现场水平诊断CA的有效诊断工具的潜力。