Literature DB >> 26192088

Innovative use of platinum compounds to selectively detect live microorganisms by polymerase chain reaction.

Takashi Soejima1, Jun-Ichi Minami2, Jin-Zhong Xiao3, Fumiaki Abe2.   

Abstract

PCR cannot distinguish live microorganisms from dead ones. To circumvent this disadvantage, ethidium/propidium-monoazide (EMA/PMA) and psoralen to discriminate live from dead bacteria have been used for 2 decades. These methods require the use of numerous laborious procedures. We introduce an innovative method that uses platinum compounds, which are primarily used as catalysts in organic chemistry and partly used as anti-cancer drugs. Microorganisms are briefly exposed to platinum compounds in vivo, and these compounds penetrate dead (compromised) microorganisms but not live ones and are chelated by chromosomal DNA. The use of platinum compounds permits clear discrimination between live and dead microorganisms in water and milk (including Cronobacter sakazakii and Escherichia coli) via PCR compared with typically used PMA. This platinum-PCR method could enable the specific detection of viable coliforms in milk at a concentration of 5-10 CFU mL(-1) specified by EU/USA regulations after a 4-h process. For sample components, environmental water contains lower levels of PCR inhibitors than milk does, and milk is similar to infant formula, skim milk and blood; thus, the use of the platinum-PCR method could also prevent food poisoning due to the presence of C. sakazakii in dairy products. This method could provide outstanding rapidity for use in environmental/food/clinical tests. Platinum-PCR could also be a substitute for the typical culture-based methods currently used.
© 2015 Wiley Periodicals, Inc.

Entities:  

Keywords:  bacteria; ethidium monoazide; pathogen; platinum; polymerase chain reaction; propidium monoazide

Mesh:

Substances:

Year:  2015        PMID: 26192088     DOI: 10.1002/bit.25711

Source DB:  PubMed          Journal:  Biotechnol Bioeng        ISSN: 0006-3592            Impact factor:   4.530


  8 in total

1.  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

2.  Viability RT-qPCR Combined with Sodium Deoxycholate Pre-treatment for Selective Quantification of Infectious Viruses in Drinking Water Samples.

Authors:  Vu Duc Canh; Ikuro Kasuga; Hiroaki Furumai; Hiroyuki Katayama
Journal:  Food Environ Virol       Date:  2019-01-24       Impact factor: 2.778

3.  A Hundred Years of Diagnosing Superficial Fungal Infections: Where Do We Come From, Where Are We Now and Where Would We Like To Go?

Authors:  Yvonne Gräser; Ditte M L Saunte
Journal:  Acta Derm Venereol       Date:  2020-04-20       Impact factor: 3.875

Review 4.  Advances and Challenges in Viability Detection of Foodborne Pathogens.

Authors:  Dexin Zeng; Zi Chen; Yuan Jiang; Feng Xue; Baoguang Li
Journal:  Front Microbiol       Date:  2016-11-22       Impact factor: 5.640

Review 5.  Detection and Enumeration of Spore-Forming Bacteria in Powdered Dairy Products.

Authors:  Aoife J McHugh; Conor Feehily; Colin Hill; Paul D Cotter
Journal:  Front Microbiol       Date:  2017-01-31       Impact factor: 5.640

6.  Capsid integrity quantitative PCR to determine virus infectivity in environmental and food applications - A systematic review.

Authors:  Mats Leifels; Dan Cheng; Emanuele Sozzi; David C Shoults; Stefan Wuertz; Skorn Mongkolsuk; Kwanrawee Sirikanchana
Journal:  Water Res X       Date:  2020-12-09

7.  A Novel Approach to the Viability Determination of Mycobacterium avium subsp. paratuberculosis Using Platinum Compounds in Combination With Quantitative PCR.

Authors:  Martina Cechova; Monika Beinhauerova; Vladimir Babak; Iva Slana; Petr Kralik
Journal:  Front Microbiol       Date:  2021-11-24       Impact factor: 5.640

8.  A viability assay combining palladium compound treatment with quantitative PCR to detect viable Mycobacterium avium subsp. paratuberculosis cells.

Authors:  Martina Cechova; Monika Beinhauerova; Vladimir Babak; Petr Kralik
Journal:  Sci Rep       Date:  2022-03-19       Impact factor: 4.379

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.