Literature DB >> 15488277

Comparison of real-time PCR methods for detection of Salmonella enterica and Escherichia coli O157:H7, and introduction of a general internal amplification control.

M M Klerks1, C Zijlstra, A H C van Bruggen.   

Abstract

The objectives of this study were to compare different real-time PCR-based methods for detection of either Salmonella spp. or E. coli O157:H7 with respect to sensitivity, precision and accuracy. In addition, a general internal amplification control (IAC) is presented, allowing prevention of false negative results. The IAC allows insight in amplification efficiency and enables a more accurate quantification with the evaluated real-time PCR methods. Implementation of the IAC with the different PCR methods did not affect the precision of the methods, but the sensitivity was reduced 10-fold. Introduction of an IAC with the Salmonella enterica specific detection method showed a shift in Ct-value (increase of target Ct-value with 0.45+/-0.17 cycles), while with the method to detect E. coli O157:H7 no influence of IAC co-amplification was observed. The quantification threshold of the methods in which the IAC was included was determined at 1 pg of target DNA (equal to 200 CFU) per reaction. Qualitative detection was feasible down to 10 fg of target DNA per reaction using both methods in which the IAC was incorporated. The adjusted methods have the potential to provide fast and sensitive detection of Salmonella spp. or E. coli O157:H7, enabling accurate quantification and preventing false negative results by using the general IAC.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15488277     DOI: 10.1016/j.mimet.2004.07.011

Source DB:  PubMed          Journal:  J Microbiol Methods        ISSN: 0167-7012            Impact factor:   2.363


  13 in total

1.  Comparison of methods of extracting Salmonella enterica serovar Enteritidis DNA from environmental substrates and quantification of organisms by using a general internal procedural control.

Authors:  M M Klerks; A H C van Bruggen; C Zijlstra; M Donnikov
Journal:  Appl Environ Microbiol       Date:  2006-06       Impact factor: 4.792

2.  Prevalence of Shiga toxin-producing Escherichia coli stx1, stx2, eaeA, and rfbE genes and survival of E. coli O157:H7 in manure from organic and low-input conventional dairy farms.

Authors:  Eelco Franz; Michel M Klerks; Oscar J De Vos; Aad J Termorshuizen; Ariena H C van Bruggen
Journal:  Appl Environ Microbiol       Date:  2007-02-02       Impact factor: 4.792

3.  Indigenous populations of three closely related Lysobacter spp. in agricultural soils using real-time PCR.

Authors:  Joeke Postma; Mirjam T Schilder; Richard A van Hoof
Journal:  Microb Ecol       Date:  2011-03-30       Impact factor: 4.552

4.  Distribution and Characterization of Salmonella enterica Isolates from Irrigation Ponds in the Southeastern United States.

Authors:  Zhiyao Luo; Ganyu Gu; Amber Ginn; Mihai C Giurcanu; Paige Adams; George Vellidis; Ariena H C van Bruggen; Michelle D Danyluk; Anita C Wright
Journal:  Appl Environ Microbiol       Date:  2015-04-24       Impact factor: 4.792

5.  Simultaneous Screening of 24 Target Genes of Foodborne Pathogens in 35 Foodborne Outbreaks Using Multiplex Real-Time SYBR Green PCR Analysis.

Authors:  Hiroshi Fukushima; Jun Kawase; Yoshiki Etoh; Kumiko Sugama; Shunshuke Yashiro; Natsuko Iida; Keiji Yamaguchi
Journal:  Int J Microbiol       Date:  2010-09-28

6.  Physiological and molecular responses of Lactuca sativa to colonization by Salmonella enterica serovar Dublin.

Authors:  M M Klerks; M van Gent-Pelzer; E Franz; C Zijlstra; A H C van Bruggen
Journal:  Appl Environ Microbiol       Date:  2007-05-18       Impact factor: 4.792

7.  Accurate quantification of microorganisms in PCR-inhibiting environmental DNA extracts by a novel internal amplification control approach using Biotrove OpenArrays.

Authors:  R van Doorn; M M Klerks; M P E van Gent-Pelzer; A G C L Speksnijder; G A Kowalchuk; C D Schoen
Journal:  Appl Environ Microbiol       Date:  2009-10-02       Impact factor: 4.792

8.  Quenched autoligation probes allow discrimination of live bacterial species by single nucleotide differences in rRNA.

Authors:  Adam P Silverman; Eric T Kool
Journal:  Nucleic Acids Res       Date:  2005-09-02       Impact factor: 16.971

Review 9.  Rapid methods for the detection of foodborne bacterial pathogens: principles, applications, advantages and limitations.

Authors:  Jodi Woan-Fei Law; Nurul-Syakima Ab Mutalib; Kok-Gan Chan; Learn-Han Lee
Journal:  Front Microbiol       Date:  2015-01-12       Impact factor: 5.640

10.  Quantitative multiplex detection of plant pathogens using a novel ligation probe-based system coupled with universal, high-throughput real-time PCR on OpenArrays.

Authors:  Ronald van Doorn; Marianna Szemes; Peter Bonants; George A Kowalchuk; Joana F Salles; Elen Ortenberg; Cor D Schoen
Journal:  BMC Genomics       Date:  2007-08-14       Impact factor: 3.969

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.