Detection of enterotoxigenic Escherichia coli by real-time polymerase chain reaction by using MGB-TaqMan probe technique.
- Author:
Juan DAI
1
;
Yu-feng LI
;
Li-xing YUAN
;
Xiao YANG
Author Information
- Publication Type:Journal Article
- MeSH: Bacterial Toxins; isolation & purification; DNA Primers; DNA Probes; DNA, Bacterial; Enterotoxigenic Escherichia coli; isolation & purification; Molecular Probe Techniques; Polymerase Chain Reaction; methods; Taq Polymerase
- From: Chinese Journal of Preventive Medicine 2008;42(2):103-106
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo develop a real-time polymerase chain reaction(PCR) based on TaqMan technology by using a new MGB probe for detecting enterotoxigenic Escherichia coli (ETEC) in paper.
METHODSPrimers and MGB probe were designed in the ecoding region of heat-stable toxin of ETEC. Real-time PCR detected ETEC by using the exterior standard method with protracting standard curves. The specificity, sensitivity, accuracy, stability of real-time PCR system was evaluated. An internal negative antithesis was added to the real-time PCR system in order to get rid of the false positive of system. Using UNG enzyme expelled the contamination of PCR reaction.
RESULTSPrimers and MGB probe were suited to the Real-time PCR. The assay showed that the method was quick, special, sensitive and stable. The real-time PCR system could detect ETEC in a large scale. The assay might be finished in two hour.
CONCLUSIONThese observations suggested that real-time PCR based on MGB probe should be an excellent candidate for a standard ETEC detection method.
