A Catalytic DNA Activated by a Specific Strain of Bacterial Pathogen

被引:94
作者
Shen, Zhifa [1 ,5 ]
Wu, Zaisheng [1 ]
Chang, Dingran [1 ]
Zhang, Wenqing [1 ]
Kha Tram [1 ]
Lee, Christine [2 ]
Kim, Peter [4 ]
Salena, Bruno J. [3 ]
Li, Yingfu [1 ]
机构
[1] McMaster Univ, Michael G DeGroote Inst Infect Dis Res, Dept Biochem & Biomed Sci, 1280 Main St W, Hamilton, ON L8S 4K1, Canada
[2] McMaster Univ, St Josephs Healthcare, Dept Pathol & Mol Med, 50 Charlton Ave E,424 Luke Wing, Hamilton, ON L8N 4A6, Canada
[3] McMaster Univ, Dept Med, 1280 Main St W, Hamilton, ON L8N 4A6, Canada
[4] Univ Guelph, Dept Math & Stat, Guelph, ON N1G 2W1, Canada
[5] Wenzhou Med Univ, Sch Lab Med & Life Sci, Wenzhou 325035, Zhejiang, Peoples R China
基金
加拿大自然科学与工程研究理事会;
关键词
aptamers; bacterial detection; biosensors; DNAzymes; in vitro selection; TRIOSE PHOSPHATE ISOMERASE; CLOSTRIDIUM-DIFFICILE; TOXIN; POLYMORPHISM; EVOLUTION; GENES; TCDC; TPI;
D O I
10.1002/anie.201510125
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Pathogenic strains of bacteria are known to cause various infectious diseases and there is a growing demand for molecular probes that can selectively recognize them. Here we report a special DNAzyme (catalytic DNA), RFD-CD1, that shows exquisite specificity for a pathogenic strain of Clostridium difficile (C. difficile). RFD-CD1 was derived by an in vitro selection approach where a random-sequence DNA library was allowed to react with an unpurified molecular mixture derived from this strain of C. difficle, coupled with a subtractive selection strategy to eliminate cross-reactivities to unintended C. difficile strains and other bacteria species. RFDCD1 is activated by a truncated version of TcdC, a transcription factor, that is unique to the targeted strain of C. difficle. Our study demonstrates for the first time that in vitro selection offers an effective approach for deriving functional nucleic acid probes that are capable of achieving strain-specific recognition of bacterial pathogens.
引用
收藏
页码:2431 / 2434
页数:4
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