Chemical Structure of Stabilizing Layers of Negatively Charged Silver Nanoparticles as an Effector of Shifts in Soil Bacterial Microbiome under Short-Term Exposure

Int J Environ Res Public Health. 2022 Nov 4;19(21):14438. doi: 10.3390/ijerph192114438.

Abstract

In this work, we have assessed the exposure of soil bacteria from potato monoculture to three types of silver nanoparticles (AgNPs) as well as silver ions (Ag+ ions) delivered in the form of silver nitrate and a commercially available fungicide. The diversity of the soil microbial community, enzymatic activity, and carbon source utilization were evaluated. It was found that only the fungicide significantly limited the abundance and activity of soil bacteria. Silver ions significantly reduced bacterial metabolic activity. In turn, one type of AgNPs prepared with the use of tannic acid (TA) increased bacterial load and activity. There was found in all AgNPs treated soils (1) a greater proportion of all types of persistent bacteria, i.e., Bacillus, Paenibacillus, and Clostridium; (2) a visible decrease in the proportion of Nocardioides, Arthrobacter, and Candidatus Solibacter; (3) almost complete depletion of Pseudomonas; (4) increase in the number of low-frequency taxa and decrease in dominant taxa compared to the control soil. Despite the general trend of qualitative changes in the bacterial community, it was found that the differences in the chemical structure of the AgNP stabilizing layers had a significant impact on the specific metabolic activity resulting from qualitative changes in the microbiome.

Keywords: biochemical activity; fungicide; silver nanoparticles; soil bacteria; surface properties.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacteria
  • Fungicides, Industrial*
  • Ions
  • Metal Nanoparticles* / chemistry
  • Microbiota*
  • Silver
  • Soil / chemistry
  • Soil Microbiology

Substances

  • Soil
  • Fungicides, Industrial
  • Silver
  • Ions

Grants and funding

The results presented in this paper were obtained as part of a comprehensive study conducted at the University of Warmia and Mazury in Olsztyn (grant No. 30.610.011-110). This work was supported by a subsidy of the Polish Ministry of Science and Higher Education for the University of Agriculture in Krakow (grant No. 010014-D011) and the statutory research fund of the Jerzy Haber Institute of Catalysis and Surface Chemistry Polish Academy of Sciences (ICSC PAS).