Development of a rapid detection method to detect tdh gene in Vibrio parahaemolyticus using 2-step ultrarapid real-time polymerase chain reaction

被引:12
作者
Kang, Min-Hee [1 ]
Kim, Il-Wook [1 ]
Lee, Dong-Woo [1 ]
Yoo, Mi-Sun [1 ]
Han, Sang-Hoon [1 ]
Yoon, Byoung-Su [1 ]
机构
[1] Kyonggi Univ, Coll Nat Sci, Dept Life Sci, Suwon 443760, South Korea
关键词
tdh; Thermostable direct hemolysin; URRT-PCR; Ultrarapid real-time PCR; Vibrio parahaemolyticus; THERMOSTABLE DIRECT HEMOLYSIN; PCR DETECTION; ASSAY; AMPLIFICATION; SHELLFISH; BACTERIA; SYSTEM;
D O I
10.1016/j.diagmicrobio.2010.08.020
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Thermostable direct hemolysin encoded by tdh gene has been considered an important virulence factor in pathogenic Vibrio parahaemolyticus. Two-step ultrarapid real-time polymerase chain reaction (URRT PCR) with a microchip was devised to detect V. parahaemolyticus carrying tdh gene. This novel method has a 6-mu L reaction volume and extremely reduces running time since one cycle can be completed in 10 s or less. Consequently, 35 cycles of URRT PCR was successfully able to detect up to 100 fg (18 copies) of genomic DNA from pathogenic V. parahaemolyticus carrying tdh gene in 6 min. These results indicate that this method is at present the most rapid detection method for tdh gene and pathogenic V. parahaemolyticus. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:21 / 29
页数:9
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