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Aerobic condition enhances bacteriostatic effects of silver nanoparticles in aquatic environment: An antimicrobial study on Pseudomonas aeruginosa

  • Zhaoyu Chen
  • , Ping Yang
  • , Zhiguo Yuan
  • , Jianhua Guo*
  • *Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

2 Downloads (CityUHK Scholars)

Abstract

The intensive applications of silver nanoparticles (AgNPs) inevitably cause continuous release of such materials into environments, as a consequence posing potential risks to microbial communities in engineered or natural ecosystems. However, the magnitude of antibacterial capacity of nanoparticles is still inconclusive, owing to influential factors such as the size of nanoparticle, microbial species, or environmental conditions. To reveal whether the presence of air would alter AgNPs ecotoxicity, Pseudomonas aeruginosa PAO1, a facultative denitrifying bacterium and an opportunity pathogen, was used to study antibacterial assays under both anaerobic and aerobic conditions. The results indicate that the respiration status of P. aeruginosa affect the ecotoxicity of AgNPs. P. aeruginosa cultured under aerobic condition were more susceptible to AgNPs than that under anaerobic condition. Aerobic condition greatly enhanced bacteriostatic effects of AgNPs but not their bactericidal effects, as the ratio of viable but nonculturable (VBNC) bacteria remained above 90% when 5 mg L-1 AgNPs applied. Our findings offer further understanding for the degree of toxicity of nanoparticles on microbial ecosystems and underscore the importance of exposure condition (e.g. oxygen) in the mode of action of AgNPs. © 2017 The Author(s).
Original languageEnglish
Article number7398
JournalScientific Reports
Volume7
Issue number1
DOIs
Publication statusPublished - 1 Dec 2017
Externally publishedYes

Bibliographical note

Publication details (e.g. title, author(s), publication statuses and dates) are captured on an “AS IS” and “AS AVAILABLE” basis at the time of record harvesting from the data source. Suggestions for further amendments or supplementary information can be sent to [email protected].

Funding

This work was supported by the Australian Research Council [project DP170104330] and Zhaoyu Chen would like to thank the China Scholarship Council for scholarship support. Jianhua Guo acknowledges the support from the Australian Research Council Future Fellowship (FT170100196). We thank Dr. Beatrice Keller and Jianguang Li, University of Queensland for FIA and HPLC analysis, and Dr. Michael Nefedov, University of Queensland for assistance with the BD FACSAria™ II flow cytometer and data analysis. This work was performed in part at the Queensland node of the Australian National Fabrication Facility. A company established under the National Collaborative Research Infrastructure Strategy to provide nano and microfabrication facilities for Australia’s researchers.

Publisher's Copyright Statement

  • This full text is made available under CC-BY 4.0. https://creativecommons.org/licenses/by/4.0/

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