2003•Zhongguo renshougonghuanbing zazhiRequires access

Multiplex PCR for detection of the three enterotoxigenic genes in enterotoxigenic Escherichia coli

Rong-Hong Hua

Open publisher page 0 citations

Abstract

A multiplex polymerase chain reaction (PCR) was developed to detect the three enterotoxigenic genes LT,STⅠ,STⅡ in enterotoxigenic Escherichia coli from porcine Three different sets of oligonucleotide primer were simultaneously used to amplify the enterotoxin genes of heat labile (LT) and heat stable (STⅠ and STⅡ) enterotoxins of ETEC These primers amplified the 110,237 or 368 base pair DNA fragments from LT,STⅠ and STⅡ genes of the restriction endonuclease,the expected target DNA fragments were obtained There was no cross reaction with the non ETEC strains The results indicate that the PCR is a rapid,sensitive and specific method for detecting ETEC

About this research paper

What this paper is about

A multiplex polymerase chain reaction (PCR) was developed to detect the three enterotoxigenic genes LT,STⅠ,STⅡ in enterotoxigenic Escherichia coli from porcine Three different sets of oligonucleotide primer were simultaneously used to amplify the enterotoxin genes of heat labile (LT) and heat stable (STⅠ and STⅡ) enterotoxins of ETEC These primers amplified the 110,237 or 368 base pair DNA fragments from LT,STⅠ and STⅡ genes of the restriction endonuclease,the expected target DNA fragments were obtained There was no cross reaction with the non ETEC strains The results indicate that the PCR is a rapid,sensitive and specific method for detecting ETEC

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 multiplex polymerase chain reaction (PCR) was developed to detect the three enterotoxigenic genes LT,STⅠ,STⅡ in enterotoxigenic Escherichia coli from porcine Three different sets of oligonucleotide primer were simultaneously used to amplify the enterotoxin genes of heat labile (LT) and heat stable (STⅠ and STⅡ) enterotoxins of ETEC These primers amplified the 110,237 or 368 base pair DNA fragments from LT,STⅠ and STⅡ genes of the restriction endonuclease,the expected target DNA fragments were obtained There was no cross reaction with the non ETEC strains The results indicate that the PCR is a rapid,sensitive and specific method for detecting ETEC

Key concepts: Enterotoxigenic Escherichia coli, Biology, Multiplex polymerase chain reaction, Enterotoxin, Polymerase chain reaction, Restriction enzyme, Primer (cosmetics), Heat-stable enterotoxin

Related papers

Back to paper searchBrowse research topicsOriginal source
Multiplex PCR for detection of the three enterotoxigenic genes in enterotoxigenic Escherichia coli — Research Paper | ScholarLens