A method for quantitative detection of Escherichia coli O157:H7 based on the polymerase chain reaction (PCR) was developed. The method used the NIH Image 1·61 software program to quantitatively analyse the intensity of the fluorescent image of the amplified PCR product. Based on the PCR with SLT1 and SLT2 primers used separately, a log-linear relationship between the numbers of cfu of E. coli O157:H7 inoculated into ground beef and the intensity of the PCR products was achieved with and without enrichment. Without enrichment, 150 cfu of E. coli O157:H7 per gram of ground beef were detected. In contrast, the detection limit decreased to 1·2 cfu g−1 of ground beef using SLT1 and SLT2 primers after 4·5 h of enrichment using modified EC broth w...
Background: Verocytotoxin Escherichia coli is a frequent and important cause of diarrhea and haemoly...
The aim of the study was to evaluate the sensitivity of two m-PCR methods for the quantitative deter...
A multiplex polymerase chain reaction (PCR) assay was designed to simplify detection of Escherichia ...
Escherichia coli O157:H7 is an important foodborne pathogen. The majority of outbreaks of this organ...
A protocol based on immunomagnetic separation (IMS) and competitive polymerase chain reaction (C-PCR...
A quantitative assay for viable Escherichia coli O157:H7 in ground beef based on immunomagnetic sepa...
Escherichia coli O157:H7 is recognized as a major human enteropathogen. Immunotechnology and DNA bas...
A protocol for detection of low numbers of E. coli O157:H7 in ground beef by nested PCR incorporatin...
A total of nine Escherichia coli O157:H7 isolates were originally isolated from imported Indian beef...
The SYBR Green I real-time PCR assay was used to quantify E. coli O157:H7 in various meat samples. P...
Sensitivity of a polymerase chain reaction (PCR) procedure was evaluated for Escherichia coli O157:H...
Escherichia coli O157 strains have been recognized as pathogenic bacteria, of which raw beef is a kn...
The aim of this paper is to describe a methodology applicable to the isolation of viable Escherichia...
This study has evaluated the use of a commercially available Rainbow agar O157 and polymerase chain ...
Since the mid-1990s, the beef industry has used a process called test and hold, wherein beef trim an...
Background: Verocytotoxin Escherichia coli is a frequent and important cause of diarrhea and haemoly...
The aim of the study was to evaluate the sensitivity of two m-PCR methods for the quantitative deter...
A multiplex polymerase chain reaction (PCR) assay was designed to simplify detection of Escherichia ...
Escherichia coli O157:H7 is an important foodborne pathogen. The majority of outbreaks of this organ...
A protocol based on immunomagnetic separation (IMS) and competitive polymerase chain reaction (C-PCR...
A quantitative assay for viable Escherichia coli O157:H7 in ground beef based on immunomagnetic sepa...
Escherichia coli O157:H7 is recognized as a major human enteropathogen. Immunotechnology and DNA bas...
A protocol for detection of low numbers of E. coli O157:H7 in ground beef by nested PCR incorporatin...
A total of nine Escherichia coli O157:H7 isolates were originally isolated from imported Indian beef...
The SYBR Green I real-time PCR assay was used to quantify E. coli O157:H7 in various meat samples. P...
Sensitivity of a polymerase chain reaction (PCR) procedure was evaluated for Escherichia coli O157:H...
Escherichia coli O157 strains have been recognized as pathogenic bacteria, of which raw beef is a kn...
The aim of this paper is to describe a methodology applicable to the isolation of viable Escherichia...
This study has evaluated the use of a commercially available Rainbow agar O157 and polymerase chain ...
Since the mid-1990s, the beef industry has used a process called test and hold, wherein beef trim an...
Background: Verocytotoxin Escherichia coli is a frequent and important cause of diarrhea and haemoly...
The aim of the study was to evaluate the sensitivity of two m-PCR methods for the quantitative deter...
A multiplex polymerase chain reaction (PCR) assay was designed to simplify detection of Escherichia ...