期刊
JOURNAL OF VETERINARY SCIENCE
卷 19, 期 2, 页码 242-250出版社
KOREAN SOC VETERINARY SCIENCE
DOI: 10.4142/jvs.2018.19.2.242
关键词
Mycobacterium avium subsp paratuberculosis; isothermal detection; lateral flow dipstick; paratuberculosis; recombinase polymerase amplification
资金
- earmarked fund for the China Agriculture Research System [CARs-37]
- Taishan Scholar and Distinguished Experts
- Shandong Province Natural Science Foundation [ZR2015PC007]
- National Natural Science Fund of China [31502064, 31672556]
- Shandong Major Agricultural Application Technology Innovation Project
- Primary Research & Development Plan of Shandong Province [2015GNC113006, 2016GNC113006]
Paratuberculosis (Johne's disease) is a chronic debilitating disease of domestic and wild ruminants. However, widespread point-of-care testing is infrequent due to the lack of a robust method. The isothermal recombinase polymerase amplification (RPA) technique has applied for rapid diagnosis. Herein, RPA combined with a lateral flow dipstick (LFD) assay was developed to estimate DNA from Mycobacterium avium subsp. paratuberculosis. First, analytical specificity and sensitivity of the RPA-nfo primer and probe sets were assessed. The assay successfully detected M. paratuberculosis DNA in 30 min at 39 degrees C with a detection limit of up to eight copies per reaction, which was equivalent to that of the real-time quantitative polymerase chain reaction (qPCR) assay. The assay was specific, as it did not amplify genomes from five other Mycobacterium spp. or five pathogenic enteric bacteria. Six hundred-twelve clinical samples (320 fecal and 292 serum) were assessed by RPA-LFD, qPCR, and enzyme-linked immunosorbent assay, respectively. The RPA-LFD assay yielded 100% sensitivity, 97.63% specificity, and 98.44% concordance rate with the qPCR results. This is the first report utilizing an RPA-LFD assay to visualize and rapidly detect M. paratuberculosis. Our results show this assay should be a useful method for the diagnosis of paratuberculosis in resource-constrained settings.
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