Mutagenesis and Resistance Development of Bacteria Challenged by Silver Nanoparticles.
Kun WuHaichao LiXiao CuiRuobing FengWeizhe ChenYuchen JiangChao TangYaohai WangYan WangXiaopeng ShenYufei LiuMichael LynchHongan LongPublished in: Antimicrobial agents and chemotherapy (2022)
Because of their extremely broad spectrum and strong biocidal power, nanoparticles of metals, especially silver (AgNPs), have been widely applied as effective antimicrobial agents against bacteria, fungi, and so on. However, the mutagenic effects of AgNPs and resistance mechanisms of target cells remain controversial. In this study, we discover that AgNPs do not speed up resistance mutation generation by accelerating genome-wide mutation rate of the target bacterium Escherichia coli. AgNPs-treated bacteria also show decreased expression in quorum sensing (QS), one of the major mechanisms leading to population-level drug resistance in microbes. Nonetheless, these nanomaterials are not immune to resistance development by bacteria. Gene expression analysis, experimental evolution in response to sublethal or bactericidal AgNPs treatments, and gene editing reveal that bacteria acquire resistance mainly through two-component regulatory systems, especially those involved in metal detoxification, osmoregulation, and energy metabolism. Although these findings imply low mutagenic risks of nanomaterial-based antimicrobial agents, they also highlight the capacity for bacteria to evolve resistance.
Keyphrases
- silver nanoparticles
- genome wide
- escherichia coli
- staphylococcus aureus
- dna methylation
- human health
- gold nanoparticles
- gene expression
- risk assessment
- cell death
- single cell
- signaling pathway
- pseudomonas aeruginosa
- copy number
- cell proliferation
- heavy metals
- binding protein
- newly diagnosed
- genome wide identification
- pi k akt
- health risk assessment