# Emergence of microbial resistance against nanoparticles: Mechanisms and strategies

**Authors:** Siya Kamat, Madhuree Kumari

PMC · DOI: 10.3389/fmicb.2023.1102615 · Frontiers in Microbiology · 2023-01-26

## TL;DR

This paper explores how bacteria develop resistance to antimicrobial nanoparticles and suggests strategies to prevent or reverse this resistance.

## Contribution

The paper identifies mechanisms of nanoparticle resistance in bacteria and proposes strategies to mitigate resistance development.

## Key findings

- Bacteria develop resistance to nanoparticles through mechanisms like oxidative stress and membrane alterations.
- Surface properties and aggregation of nanoparticles influence resistance development.
- Modifying nanoparticle surface corona or inhibiting flagellin production can reverse resistance.

## Abstract

Antimicrobial nanoparticles have gained the status of a new generation of drugs that can kill bacterial pathogens by multiple means; however, nanoparticle resistance acquired by some bacterial pathogens has evoked a cause of concern. Several reports suggested that bacteria can develop nanoparticles, specifically metal nanoparticle resistance, by mechanisms: nanoparticle transformation-induced oxidative stress, membrane alterations, reversible adaptive resistance, irreversible modifications to cell division, and a change in bacterial motility and resistance. Surface properties, concentration and aggregation of nanoparticles, biofilm forming and metal exclusion capacity, and R plasmid and flagellin synthesis by bacteria are crucial factors in the development of nanoparticle resistance in bacteria. Studies reported the resistance reversal by modifying the surface corona of nanoparticles or inhibiting flagellin production by bacterial pathogens. Furthermore, strict regulation regarding the use and disposal of nano-waste across the globe, the firm knowledge of microbe–nanoparticle interaction, and the regulated disposal of nanoparticles in soil and water is required to prevent microbes from developing nanoparticle resistance.

## Full-text entities

- **Genes:** SilP [NCBI Gene 3244868], SilE [NCBI Gene 13909321], cusS (sensor histidine kinase CusS) [NCBI Gene 945978] {aka ECK0562, ybcZ}, thioredoxin [NCBI Gene 28380422], CRP [NCBI Gene 20468888]
- **Diseases:** MDR (MESH:D018088), autoimmune diseases (MESH:D001327), resistance (MESH:D060467), cancer (MESH:D009369), microbial infection (MESH:D015163), bacterial (MESH:D001424), diabetes (MESH:D003920), respiratory disorders (MESH:D012131), HIV (MESH:D015658), toxicity (MESH:D064420)
- **Species:** Escherichia coli str. K-12 substr. MG1655 (no rank) [taxon 511145], Plasmodium falciparum (malaria parasite P. falciparum, species) [taxon 5833], Candida albicans (species) [taxon 5476], Pseudomonas putida F1 (strain) [taxon 351746], Staphylococcus aureus (species) [taxon 1280], Escherichia coli (E. coli, species) [taxon 562], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Homo sapiens (human, species) [taxon 9606], Bacillus sp. (in: firmicutes) (species) [taxon 1409], Pseudomonas aeruginosa (species) [taxon 287], Escherichia coli BW25113 (no rank) [taxon 679895], Penicillium griseofulvum (species) [taxon 5078], Penicillium chrysogenum (species) [taxon 5076], Mycobacterium tuberculosis (species) [taxon 1773], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Escherichia coli K-12 (strain) [taxon 83333], Salmonella enterica subsp. enterica serovar Typhimurium (no rank) [taxon 90371]
- **Mutations:** serine to tyrosine at position 169, ATC to -TC, TCT to TAT
- **Cell lines:** MK — Macaca fascicularis (Crab-eating macaque), Spontaneously immortalized cell line (CVCL_3631)

## Full text

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## Figures

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## References

66 references — full list in the complete paper: https://tomesphere.com/paper/PMC9909277/full.md

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Source: https://tomesphere.com/paper/PMC9909277