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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.
Abstract:
Multi-antibiotic resistant (MAR) bacteria cost billions in medical care and tens of thousands of lives annually but perennial calls to limit agricultural and other misuse of antibiotics and to fund antibiotic discovery have not slowed this MAR deluge. Since mobile genetic elements (MGEs) stitch single antibiotic resistance genes into clinically significant MAR arrays, it is high time to focus on how MGEs generate MAR and how disabling them could ameliorate the MAR problem. However, to consider only antibiotics as the drivers of MAR is to miss the significant impact of exposure to non-antibiotic toxic chemicals, specifically metals, on the persistence and spread of MAR. Toxic metals were among the earliest discovered targets of plasmid-encoded resistance genes. Recent genomic epidemiology clearly demonstrated the co-prevalence of metal resistances and antibiotic multi-resistance, uniquely in humans and domestic animals. Metal resistances exploit the same, ancient "transportation infrastructure" of plasmids, transposons, and integrons that spread the antibiotic resistance genes and will continue to do so even if all antibiotic misuse were stopped today and new antibiotics were flowing from the pipeline monthly. In a key experiment with primates, continuous oral exposure to mercury (Hg) released from widely used dental amalgam fillings co-selected for MAR bacteria in the oral and fecal commensal microbiomes and, most importantly, when amalgams were replaced with non-metal fillings, MAR bacteria declined dramatically. Could that also be happening on the larger public health scale as use of amalgam restorations is curtailed or banned in many countries? This commentary covers salient past and recent findings of key metal-antibiotic resistance associations and proposes that the shift from phenotyping to genotyping in surveillance of resistance loci will allow a test of whether declining exposure to this leading source of Hg is accompanied by a decline in MAR compared to countries where amalgam is still used. If this hypothesis is correct, the limited success of antibiotic stewardship practices may be because MAR is also being driven by continuous, daily exposure to Hg, a non-antibiotic toxicant widely used in humans.
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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