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重组酶聚合酶扩增法检测日本血吸虫病的实验小鼠和山羊模型的建立。

Development of a Recombinase Polymerase Amplification Assay for Schistosomiasis Japonica Diagnosis in the Experimental Mice and Domestic Goats.

机构信息

National Reference Laboratory for Animal Schistosomiasis, Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Shanghai, China.

Key Laboratory of Animal Parasitology of Ministry of Agriculture, Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Shanghai, China.

出版信息

Front Cell Infect Microbiol. 2021 Nov 16;11:791997. doi: 10.3389/fcimb.2021.791997. eCollection 2021.

Abstract

Although the prevalence of schistosomiasis japonica has declined gradually in China, more accurate and sensitive diagnostic methods are urgently needed for the prevention and control of this disease. Molecular diagnostic methods are advantageous in terms of sensitivity and specificity, but they are time-consuming and require expensive instruments and skilled personnel, which limits their application in low-resource settings. In this study, an isothermal DNA amplification assay and recombinase polymerase amplification (RPA) combined with lateral flow dipstick (LFD) were set up. It was used to detect infections in experimental mice and domestic goats by amplifying a specific DNA fragment of . The lower limit of detection for the LFD-RPA assay was evaluated using dilutions of plasmid containing the target sequence. Cross-reactivity was evaluated using genomic DNA from eight other parasites. The effectiveness of the LFD-RPA assay was verified by assessing 36 positive plasma samples and 36 negative plasma samples from mice. The LFD-RPA assay and real-time PCR were also used to assess 48 schistosomiasis japonica-positive plasma samples and 53 negative plasma samples from goats. The LFD-RPA assay could detect 2.6 femtogram (fg) of target DNA (~39 fg genomic DNA of ), only 10-fold less sensitive than real-time PCR assay. There was no cross-reactivity with DNA from the other eight parasites, such as and . The whole amplification process could be completed within 15 min at 39°C, and the results can be observed easily using the LFD. The sensitivity and specificity of the LFD-RPA assay were 97.22% (35/36, 95% CI, 85.47%-99.93%) and 100% (36/36, 95% CI, 90.26%-100%) in mice, and 93.75% (45/48, 95% CI, 82.80%-98.69%) and 100% (53/53, 95% CI, 93.28%-100%) in goats. By comparison, the sensitivity and specificity of real-time PCR were 100% (36/36, 95% CI, 90.26%-100%) and 100% (36/36, 95% CI, 90.26%-100%) for mice, and 97.92% (47/48, 95% CI, 88.93%-99.95%) and 100% (53/53, 95% CI, 93.28%-100%) for goats. The LFD-RPA assay exhibits high sensitivity and specificity for the diagnosis of schistosomiasis japonica, and it is an alternative method for diagnosis schistosomiasis japonica in low resource setting.

摘要

尽管日本血吸虫病在中国的流行已逐渐下降,但仍迫切需要更准确和敏感的诊断方法来预防和控制这种疾病。分子诊断方法在灵敏度和特异性方面具有优势,但需要昂贵的仪器和熟练的人员,这限制了它们在资源匮乏环境中的应用。在这项研究中,建立了一种等温 DNA 扩增检测和重组酶聚合酶扩增(RPA)结合侧流试纸(LFD),用于检测实验小鼠和家养山羊中的 感染。通过扩增含有靶序列的质粒的稀释液来评估 LFD-RPA 检测的检测下限。使用来自其他 8 种寄生虫的基因组 DNA 评估交叉反应性。通过评估 36 份来自小鼠的阳性血浆样本和 36 份阴性血浆样本来验证 LFD-RPA 检测的有效性。还使用 LFD-RPA 检测和实时 PCR 评估了来自 48 份日本血吸虫病阳性血浆样本和 53 份阴性血浆样本的 。LFD-RPA 检测可以检测到 2.6 飞克(fg)的 靶 DNA(~39 fg 基因组 DNA 的 ),仅比实时 PCR 检测低 10 倍。与来自其他 8 种寄生虫的 DNA (如 和 )没有交叉反应。整个扩增过程可在 39°C 下 15 分钟内完成,使用 LFD 可轻松观察到结果。LFD-RPA 检测在小鼠中的灵敏度和特异性分别为 97.22%(35/36,95%CI,85.47%-99.93%)和 100%(36/36,95%CI,90.26%-100%),在山羊中的灵敏度和特异性分别为 93.75%(45/48,95%CI,82.80%-98.69%)和 100%(53/53,95%CI,93.28%-100%)。相比之下,实时 PCR 在小鼠中的灵敏度和特异性分别为 100%(36/36,95%CI,90.26%-100%)和 100%(36/36,95%CI,90.26%-100%),在山羊中的灵敏度和特异性分别为 97.92%(47/48,95%CI,88.93%-99.95%)和 100%(53/53,95%CI,93.28%-100%)。LFD-RPA 检测对日本血吸虫病的诊断具有较高的灵敏度和特异性,是资源匮乏环境中诊断日本血吸虫病的一种替代方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00c6/8635165/c1f12cc93689/fcimb-11-791997-g001.jpg

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