Literature DB >> 18448692

Method To Detect Only Live Bacteria during PCR Amplification.

Takashi Soejima1, Ken-ichiro Iida, Tian Qin, Hiroaki Taniai, Masanori Seki, Shin-ichi Yoshida.   

Abstract

Ethidium monoazide (EMA) is a DNA cross-linking agent and eukaryotic topoisomerase II poison. We previously reported that the treatment of EMA with visible light irradiation (EMA + Light) directly cleaved chromosomal DNA of Escherichia coli (T. Soejima, K. Iida, T. Qin, H. Taniai, M. Seki, A. Takade, and S. Yoshida, Microbiol. Immunol. 51:763-775, 2007). Herein, we report that EMA + Light randomly cleaved chromosomal DNA of heat-treated, but not live, Listeria monocytogenes cells within 10 min of treatment. When PCR amplified DNA that was 894 bp in size, PCR final products from 10(8) heat-treated L. monocytogenes were completely suppressed by EMA + Light. When target DNA was short (113 bp), like the hly gene of L. monocytogenes, DNA amplification was not completely suppressed by EMA + Light only. Thus, we used DNA gyrase/topoisomerase IV and mammalian topoisomerase poisons (here abbreviated as T-poisons) together with EMA + Light. T-poisons could penetrate heat-treated, but not live, L. monocytogenes cells within 30 min to cleave chromosomal DNA by poisoning activity. The PCR product of the hly gene from 10(8) heat-treated L. monocytogenes cells was inhibited by a combination of EMA + Light and T-poisons (EMA + Light + T-poisons), but those from live bacteria were not suppressed. As a model for clinical application to bacteremia, we tried to discriminate live and antibiotic-treated L. monocytogenes cells present in human blood. EMA + Light + T-poisons completely suppressed the PCR product from 10(3) to 10(7) antibiotic-treated L. monocytogenes cells but could detect 10(2) live bacteria. Considering the prevention and control of food poisoning, this method was applied to discriminate live and heat-treated L. monocytogenes cells spiked into pasteurized milk. EMA + Light + T-poisons inhibited the PCR product from 10(3) to 10(7) heat-treated cells but could detect 10(1) live L. monocytogenes cells. Our method is useful in clinical as well as food hygiene tests.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 18448692      PMCID: PMC2446937          DOI: 10.1128/JCM.02171-07

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  36 in total

Review 1.  Development and application of new nucleic acid-based technologies for microbial community analyses in foods.

Authors:  Knut Rudi; Hege K Nogva; Birgitte Moen; Hilde Nissen; Sylvia Bredholt; Trond Møretrø; Kristine Naterstad; Askild Holck
Journal:  Int J Food Microbiol       Date:  2002-09-15       Impact factor: 5.277

2.  Intercalative antitumor drugs interfere with the breakage-reunion reaction of mammalian DNA topoisomerase II.

Authors:  K M Tewey; G L Chen; E M Nelson; L F Liu
Journal:  J Biol Chem       Date:  1984-07-25       Impact factor: 5.157

3.  New monofunctional reagents for DNA as possible agents for the photochemotherapy of psoriasis: derivatives of 4,5'-dimethylangelicin.

Authors:  F Dall'Acqua; D Vedaldi; S Caffieri; A Guiotto; P Rodighiero; F Baccichetti; F Carlassare; F Bordin
Journal:  J Med Chem       Date:  1981-02       Impact factor: 7.446

4.  Ethidium monoazide for DNA-based differentiation of viable and dead bacteria by 5'-nuclease PCR.

Authors:  Hege Karin Nogva; Signe Marie Drømtorp; Hilde Nissen; Knut Rudi
Journal:  Biotechniques       Date:  2003-04       Impact factor: 1.993

5.  Mechanism of antitumor drug action: poisoning of mammalian DNA topoisomerase II on DNA by 4'-(9-acridinylamino)-methanesulfon-m-anisidide.

Authors:  E M Nelson; K M Tewey; L F Liu
Journal:  Proc Natl Acad Sci U S A       Date:  1984-03       Impact factor: 11.205

6.  Application of oligonucleotide array technology for the rapid detection of pathogenic bacteria of foodborne infections.

Authors:  Bang-Xing Hong; Li-Fang Jiang; Yu-Shan Hu; Dan-Yun Fang; Hui-Yu Guo
Journal:  J Microbiol Methods       Date:  2004-09       Impact factor: 2.363

7.  Single dose ciprofloxacin for the eradication of pharyngeal carriage of Neisseria meningitidis.

Authors:  P N Gaunt; B E Lambert
Journal:  J Antimicrob Chemother       Date:  1988-04       Impact factor: 5.790

8.  Termination sites of the in vitro nick-translation reaction on DNA that had photoreacted with psoralen.

Authors:  J G Piette; J E Hearst
Journal:  Proc Natl Acad Sci U S A       Date:  1983-09       Impact factor: 11.205

9.  Clinical efficacy and levels of ciprofloxacin in tissue in patients with soft tissue infection.

Authors:  C M Licitra; R G Brooks; B E Sieger
Journal:  Antimicrob Agents Chemother       Date:  1987-05       Impact factor: 5.191

10.  Characterization of a camptothecin-resistant human DNA topoisomerase I.

Authors:  E Kjeldsen; B J Bonven; T Andoh; K Ishii; K Okada; L Bolund; O Westergaard
Journal:  J Biol Chem       Date:  1988-03-15       Impact factor: 5.157

View more
  18 in total

1.  Viable and Total Bacterial Populations Undergo Equipment- and Time-Dependent Shifts during Milk Processing.

Authors:  Mary E Kable; Yanin Srisengfa; Zhengyao Xue; Laurynne C Coates; Maria L Marco
Journal:  Appl Environ Microbiol       Date:  2019-06-17       Impact factor: 4.792

2.  Selective quantification of viable Escherichia coli bacteria in biosolids by quantitative PCR with propidium monoazide modification.

Authors:  Bilgin Taskin; Ayse Gul Gozen; Metin Duran
Journal:  Appl Environ Microbiol       Date:  2011-05-20       Impact factor: 4.792

3.  The Integration of Gold Nanoparticles with Polymerase Chain Reaction for Constructing Colorimetric Sensing Platforms for Detection of Health-Related DNA and Proteins.

Authors:  Wanhe Wang; Xueliang Wang; Jingqi Liu; Chuankai Lin; Jianhua Liu; Jing Wang
Journal:  Biosensors (Basel)       Date:  2022-06-16

4.  Innovative Use of Palladium Compounds To Selectively Detect Live Enterobacteriaceae in Milk by PCR.

Authors:  Takashi Soejima; Kei-Ji Iwatsuki
Journal:  Appl Environ Microbiol       Date:  2016-09-23       Impact factor: 4.792

5.  Viability PCR, a culture-independent method for rapid and selective quantification of viable Legionella pneumophila cells in environmental water samples.

Authors:  Pilar Delgado-Viscogliosi; Lydie Solignac; Jean-Marie Delattre
Journal:  Appl Environ Microbiol       Date:  2009-04-10       Impact factor: 4.792

6.  Genome-Wide fitness analysis of group B Streptococcus in human amniotic fluid reveals a transcription factor that controls multiple virulence traits.

Authors:  Allison N Dammann; Anna B Chamby; Andrew J Catomeris; Kyle M Davidson; Hervé Tettelin; Jan-Peter van Pijkeren; Kathyayini P Gopalakrishna; Mary F Keith; Jordan L Elder; Adam J Ratner; Thomas A Hooven
Journal:  PLoS Pathog       Date:  2021-03-08       Impact factor: 6.823

7.  Experimental design for the optimization of propidium monoazide treatment to quantify viable and non-viable bacteria in piggery effluents.

Authors:  Jérémy Desneux; Marianne Chemaly; Anne-Marie Pourcher
Journal:  BMC Microbiol       Date:  2015-08-16       Impact factor: 3.605

8.  Distribution and Diversity of Pathogenic Leptospira Species in Peri-domestic Surface Waters from South Central Chile.

Authors:  Meghan R Mason; Carolina Encina; Srinand Sreevatsan; Claudia Muñoz-Zanzi
Journal:  PLoS Negl Trop Dis       Date:  2016-08-16

9.  Method to quantify live and dead cells in multi-species oral biofilm by real-time PCR with propidium monoazide.

Authors:  Gerard Alvarez; Marta González; Sergio Isabal; Vanessa Blanc; Rubén León
Journal:  AMB Express       Date:  2013-01-04       Impact factor: 3.298

10.  Development of a sensitive and specific qPCR assay in conjunction with propidium monoazide for enhanced detection of live Salmonella spp. in food.

Authors:  Baoguang Li; Jin-Qiang Chen
Journal:  BMC Microbiol       Date:  2013-12-01       Impact factor: 3.605

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.