Thinking outside the (pill) box: Does toxic metal exposure thwart antibiotic stewardship best practices?

Andrew G Wiggins1, Stephen P LaVoie2, Joy Wireman1

  • 1Department of Microbiology, The University of Georgia, Athens 30602, Georgia.

Plasmid
|September 9, 2018
PubMed

Insights

Toxic metals, particularly mercury from dental amalgams, drive multi-antibiotic resistant (MAR) bacteria. Reducing mercury exposure may decrease MAR bacteria, offering a new public health strategy beyond antibiotic stewardship.

Area of Science:

  • Microbiology and Public Health
  • Environmental Toxicology
  • Genomic Epidemiology

Background:

  • Multi-antibiotic resistant (MAR) bacteria pose a significant global health threat, causing substantial mortality and healthcare costs.
  • Current strategies focusing solely on antibiotic stewardship and discovery have not curbed the rise of MAR bacteria.
  • Mobile genetic elements (MGEs) are key drivers in the dissemination of antibiotic resistance genes, forming MAR arrays.

Purpose of the Study:

  • To investigate the role of non-antibiotic toxic chemicals, specifically metals, in the persistence and spread of MAR bacteria.
  • To explore the association between metal resistance and antibiotic multi-resistance, particularly in human and animal microbiomes.
  • To propose a hypothesis linking mercury exposure from dental amalgams to the prevalence of MAR bacteria and to suggest a method for testing this link.

Main Methods:

  • Review of existing literature on metal-antibiotic resistance associations.
  • Analysis of genomic epidemiology data showing co-prevalence of metal and antibiotic resistance.
  • Discussion of a primate experiment demonstrating mercury's co-selection of MAR bacteria and the impact of amalgam removal.

Main Results:

  • Genomic epidemiology reveals a strong co-prevalence of metal resistances and antibiotic multi-resistance in humans and domestic animals.
  • A primate study showed continuous mercury exposure from dental amalgams selected for MAR bacteria, which declined upon amalgam replacement.
  • Metal resistance genes utilize the same MGEs (plasmids, transposons, integrons) that spread antibiotic resistance.

Conclusions:

  • Exposure to toxic metals, especially mercury, is a significant co-driver of MAR bacteria, independent of antibiotic use.
  • Reducing mercury exposure, such as by phasing out dental amalgams, could be an effective public health strategy to combat MAR bacteria.
  • Future surveillance shifting from phenotyping to genotyping of resistance loci can test the hypothesis that declining mercury exposure correlates with reduced MAR prevalence.

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