Literature DB >> 17668025

Highly chlorinated Escherichia coli cannot be stained by propidium iodide.

M-H Phe1, M Dossot, H Guilloteau, J-C Block.   

Abstract

Several studies have shown that the staining by fluorochromes (DAPI, SYBR Green II, and TOTO-1) of bacteria is altered by chlorination. To evaluate the effect of chlorine (bleach solution) on propidium iodide (PI) staining, we studied Escherichia coli in suspension and biomolecules in solution (DNA, RNA, BSA, palmitic acid, and dextran) first subjected to chlorine and then neutralized by sodium thiosulphate. The suspensions and solutions were subsequently stained with PI. The fluorescence intensity of the PI-stained DNA and RNA in solution dramatically decreased with an increase in the chlorine concentration applied. These results explain the fact that for chlorine concentrations higher than 3 micromol/L Cl2, the E. coli cells were too damaged to be properly stained by PI. In the case of highly chlorinated bacteria, it was impossible to distinguish healthy cells (with a PI-impermeable membrane and undamaged nucleic acids), which were nonfluorescent after PI staining, from cells severely injured by chlorine (with a PI-permeable membrane and damaged nucleic acids) that were also nonfluorescent, as PI penetrated but did not stain chlorinated nucleic acids. Our results suggest that it would be prudent to be cautious in interpreting the results of PI staining, as PI false-negative cells (cells with compromised membranes but not stained by PI because of nucleic acid damage caused by chlorine) are obtained as a result of nucleic acid damage, leading to an underestimation of truly dead bacteria.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17668025     DOI: 10.1139/W07-022

Source DB:  PubMed          Journal:  Can J Microbiol        ISSN: 0008-4166            Impact factor:   2.419


  6 in total

1.  Agreement, precision, and accuracy of epifluorescence microscopy methods for enumeration of total bacterial numbers.

Authors:  Eun-Young Seo; Tae-Seok Ahn; Young-Gun Zo
Journal:  Appl Environ Microbiol       Date:  2010-01-22       Impact factor: 4.792

2.  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

3.  Combining Microscopy Assays of Bacteria-Surface Interactions To Better Evaluate Antimicrobial Polymer Coatings.

Authors:  M K L N Sikosana; A Ruland; C Werner; L D Renner
Journal:  Appl Environ Microbiol       Date:  2022-02-02       Impact factor: 5.005

4.  Comparison between Flow Cytometry and Traditional Culture Methods for Efficacy Assessment of Six Disinfectant Agents against Nosocomial Bacterial Species.

Authors:  Richard Massicotte; Akier A Mafu; Darakhshan Ahmad; Francis Deshaies; Gilbert Pichette; Pierre Belhumeur
Journal:  Front Microbiol       Date:  2017-02-03       Impact factor: 5.640

5.  Assessment of Damage to Nucleic Acids and Repair Machinery in Salmonella typhimurium Exposed to Chlorine.

Authors:  M H Phe; M Hajj Chehade; H Guilloteau; C Merlin; J C Block
Journal:  Int J Microbiol       Date:  2009-07-19

6.  Evaluation by Flow Cytometry of Escherichia coli Viability in Lettuce after Disinfection.

Authors:  Pilar Teixeira; Bruna Fernandes; Ana Margarida Silva; Nicolina Dias; Joana Azeredo
Journal:  Antibiotics (Basel)       Date:  2019-12-31
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.