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作 者:ZHANG Zheng YU Yongxiang CHEN Jing WANG Yingeng JIANG Yong LIAO Meijie RONG Xiaojun ZHANG Hao
机构地区:[1]Key Laboratory of Maricultural Organism Disease Control,Ministry of Agriculture and Rural Affairs,Yellow Sea Fisheries Research Institute,Chinese Academic of Fishery Sciences,Qingdao 266071,China [2]Laboratory for Marine Fisheries Science and Food Production Processes,Qingdao National Laboratory for Marine Science and Technology,Qingdao 266237,China [3]National Oceanographic Center,Qingdao 266071,China
出 处:《Journal of Ocean University of China》2021年第2期445-453,共9页中国海洋大学学报(英文版)
基 金:supported by the National Key Research and Development Program of China (No. 2019YFD0900104);the Key Projects of Science and Technology In-novation of Shandong Province (No. 2018YFJH0703)。
摘 要:As a marine bacterial pathogen, Photobacterium damselae subsp. damselae(PDD) is distributed in seawater worldwide. It can infect different animals as well as humans, even cause deaths. The highly conserved regions of PDD mcp gene on chromosome and dly gene on plasmid were selected as the target fragments to design the specific primers. Recombinant plasmid standard was prepared based on the primers. With GENECHECKER UF-150 qRT-PCR instrument as the platform, a fluorescence-based quantitative real-time PCR(qRT-PCR) method was established for the detection of PDD. This method can specifically detect PDD and distinguish the highly virulent strains. Additionally, the test results can be qualitatively judged by visualization, while the quantitative detection can be achieved through the standard curve calculation. The minimum limit of detection was 1.0×101 copies μL-1, and the detection time was less than 20 min. In summary, this new method has outstanding advantages, such as strong specificity, high sensitivity, and low site requirements. It is a rapid on-site detection technology for highly virulent PDD strains.
关 键 词:MARICULTURE Photobacterium damselae MICROFLUIDICS PATHOGENICITY rapid detection
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