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  4. Flow cytometry study of Escherichia coli treated with plasma-activated water: confirming the absence of the viable but non-culturable state in bacteria
 
research article

Flow cytometry study of Escherichia coli treated with plasma-activated water: confirming the absence of the viable but non-culturable state in bacteria

Agus, Rita  
•
Avino, Fabio  
•
Lavrikova, Aleksandra  
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2025
Frontiers in Microbiology

Plasma-activated water (PAW) is an emerging antimicrobial agent with promising applications in bacterial inactivation. The PAW samples are generated by non-contact exposure of deionized water to a surface dielectric barrier discharge plasma and are characterized by a reactive nitrogen species-rich chemistry. In this work, fluorescence flow cytometry is applied to assess the viability of Escherichia coli treated with PAW. The results indicate that PAW exhibits a strong bactericidal effect, significantly increasing propidium iodide positive populations and leading to cell shrinkage. Comparative colony-forming unit counting confirmed these findings, showing agreement between both techniques and ruling out the possibility of a viable but non-culturable (VBNC) bacteria state. These results underscore the potential of the PAW samples produced with the present setup for safe decontamination applications, while also offering insights into the mechanisms of bacterial inactivation.

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Type
research article
DOI
10.3389/fmicb.2025.1592471
Author(s)
Agus, Rita  

École Polytechnique Fédérale de Lausanne

Avino, Fabio  

École Polytechnique Fédérale de Lausanne

Lavrikova, Aleksandra  

École Polytechnique Fédérale de Lausanne

Myers, Brayden  

École Polytechnique Fédérale de Lausanne

Furno, Ivo  

École Polytechnique Fédérale de Lausanne

Date Issued

2025

Publisher

Frontiers Media SA

Published in
Frontiers in Microbiology
Volume

16

Article Number

1592471

Subjects

flow cytometry

•

live/dead BacLight PI/SYTO9 staining

•

low-temperature plasmas (LTPs)

•

Plasma-activated water (PAW)

•

viable but non-culturable bacteria

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
SPC-LTP2A  
SPC-PP  
FunderFunding(s)Grant NumberGrant URL

Swiss Federal Institute of Technology in Lausanne

Available on Infoscience
June 26, 2025
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/251577
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