生物
副溶血性弧菌
类志贺邻单胞菌
微生物学
霍乱弧菌
多重聚合酶链反应
多路复用
创伤弧菌
聚合酶链反应
细菌
基因
遗传学
作者
Hongxia Guan,Panpan Xue,Haijian Zhou,Dan Sha,Duochun Wang,He Gao,Jie Li,Baowei Diao,Hongqun Zhao,Biao Kan,Jingyun Zhang
标识
DOI:10.1016/j.mcp.2020.101689
摘要
A multiplex PCR (mPCR) assay was established to detect five pathogenic Vibrio species and Plesiomonas shigelloides. Twelve genes were included: ompW, ctxA, rfbN, and wbfR from V. cholerae; tl, tdh, and trh from V. parahaemolyticus; toxR and vmhA from V. mimicus; toxR from V. fluvialis; vvhA from V. vulnificus; and the 23S rRNA gene from P. shigelloides. The specificity of the mPCR assay was 100% for the detection of 136 strains and the limits of detection (LoD) were 12.5–50 pg/reaction. The assay exhibited higher sensitivity than cultivation methods in the detection of APW cultures of 113 diarrhea samples. In the analysis of 369 suspected Vibrio populations from estuarine water samples, the specificity of the mPCR for V. cholerae and V. parahaemolyticus was 100% for both, while the sensitivities were 100% and 96.1%, respectively. The assay can be applied to screen enrichment cultures and suspected colonies from environmental and clinical samples.
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