2011•Food ScienceRequires access

Real-time PCR Detection of Specific Gene in Escherichia coli O157:H7

Yabin Wang

Open publisher page 0 citations

Abstract

A real-time PCR method was developed for the rapid and specific detection of Escherichia coli O157:H7.A pair of primers was designed according to the conserved sequence of rfbE gene in Escherichia coli O157:H7.The SYBR Green I real-time PCR method for detecting Escherichia coli O157:H7 was established.The sensitivity and specificity of this method was analyzed through the comparison with traditional PCR methods.The results indicated that the developed SYBR Green I real-time PCR method had the characteristics of excellent specificity,sensitivity and repeatability.The sensitivity of this developed method was 2 × 101 CFU/mL in pure cultures and 1 × 102 CFU/mL in artificially contaminated meat samples.In addition,the established method was also used for the detection of clinical samples.The results showed that the detection rate of real-time PCR for Escherichia coli O157:H7 was significantly increased when compared with traditional PCR.Therefore,the established real-time PCR method is a rapid,specific and sensitive method for the detection of Escherichia coli O157:H7.

About this research paper

What this paper is about

A real-time PCR method was developed for the rapid and specific detection of Escherichia coli O157:H7.A pair of primers was designed according to the conserved sequence of rfbE gene in Escherichia coli O157:H7.The SYBR Green I real-time PCR method for detecting Escherichia coli O157:H7 was established.The sensitivity and specificity of this method was analyzed through the comparison with traditional PCR methods.The results indicated that the developed SYBR Green I real-time PCR method had the characteristics of excellent specificity,sensitivity and repeatability.The sensitivity of this developed method was 2 × 101 CFU/mL in pure cultures and 1 × 102 CFU/mL in artificially contaminated meat samples.In addition,the established method was also used for the detection of clinical samples.The results showed that the detection rate of real-time PCR for Escherichia coli O157:H7 was significantly increased when compared with traditional PCR.Therefore,the established real-time PCR method is a rapid,specific and sensitive method for the detection of Escherichia coli O157:H7.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

A real-time PCR method was developed for the rapid and specific detection of Escherichia coli O157:H7.A pair of primers was designed according to the conserved sequence of rfbE gene in Escherichia coli O157:H7.The SYBR Green I real-time PCR method for detecting Escherichia coli O157:H7 was established.The sensitivity and specificity of this method was analyzed through the comparison with traditional PCR methods.The results indicated that the developed SYBR Green I real-time PCR method had the characteristics of excellent specificity,sensitivity and repeatability.The sensitivity of this developed method was 2 × 101 CFU/mL in pure cultures and 1 × 102 CFU/mL in artificially contaminated meat samples.In addition,the established method was also used for the detection of clinical samples.The results showed that the detection rate of real-time PCR for Escherichia coli O157:H7 was significantly increased when compared with traditional PCR.Therefore,the established real-time PCR method is a rapid,specific and sensitive method for the detection of Escherichia coli O157:H7.

Key concepts: Escherichia coli, Real-time polymerase chain reaction, Biology, SYBR Green I, Polymerase chain reaction, Repeatability, Molecular biology, Gene

Related papers

Back to paper searchBrowse research topicsOriginal source
Real-time PCR Detection of Specific Gene in Escherichia coli O157:H7 — Research Paper | ScholarLens