What was reviewed?
This comprehensive review article examines the complex interplay between metal(-loid)s and host-microbiota systems, with particular emphasis on the gut-brain axis. The review critically analyzes state-of-the-art omic methodologies—including metallomics, metabolomics, metagenomics, metatranscriptomics, and metaproteomics for assessing how both toxic and essential metals influence microbial communities and host health. It highlights how the chemical speciation of metals determines their toxicity or essentiality and explores the bidirectional communication between gut microbiota and neurological function, providing a crucial framework for understanding metal-microbiota interactions relevant to heavy metal certification programs.
Who was reviewed?
The review synthesizes evidence from a broad range of experimental models and human studies examining metal-microbiota interactions. This includes research conducted on mammalian models such as mice, rats, and pigs exposed to various metal(-loid)s like arsenic, cadmium, lead, mercury, copper, manganese, selenium, and iodine. The analysis also encompasses human population studies, particularly those investigating correlations between heavy metal exposure, gut microbiota composition, and health outcomes, including neurodevelopmental disorders such as autism spectrum disorder.
Most Important Findings
| Finding Category | Specific Details Relevant to Certification |
|---|---|
| Metal-Microbiota Interplay | Exposure to toxic metals (As, Cd, Pb, Hg) causes gut dysbiosis, altering microbial diversity and composition. Essential elements (Se, I) can modulate microbiota and potentially counteract toxicity. The chemical form (speciation) of a metal determines its biological impact and toxicity. |
| Impact on Gut-Brain Axis | Metal-induced dysbiosis affects the production of microbial metabolites (e.g., neurotransmitters like serotonin, SCFAs), influencing neurological health and potentially contributing to disorders like ASD, highlighting a novel pathway for metal toxicity. |
| Analytical Methodologies | Omic approaches are essential for a holistic view. ICP-MS is key for metallomics and heteroatom-tagged proteomics, allowing absolute quantification of metal-containing biomolecules. Metagenomics, metabolomics, and metaproteomics together reveal “who is there, what they can do, and what they are doing.” |
| Sampling & Standardization | Faecal samples are most common for microbiome studies, but storage conditions (immediate freezing at -80°C is gold standard) and DNA extraction methods significantly impact results, underscoring the need for standardized protocols in monitoring and certification. |
| Key Metal-Specific Effects | Arsenic exposure increases Bacteroidetes and decreases Firmicutes. Cadmium exposure alters ratios of Firmicutes/Bacteroidetes and reduces beneficial Lactobacillus. Lead and mercury exposures also induce distinct, reproducible shifts in microbial community structure. |
Key implications
Understanding metal-microbiota interactions has primary regulatory impacts, suggesting that safety assessments should consider microbiome disruption as an endpoint. Certification requirements must evolve to include standardized metagenomic and metallomic profiling for products. Industry applications include developing probiotics or prebiotics to mitigate metal toxicity. Significant research gaps remain in understanding low-dose chronic effects and the precise mechanisms within the gut-brain axis. Practical recommendations emphasize implementing strict sampling protocols and leveraging multi-omic approaches for comprehensive risk evaluation in heavy metal certification frameworks.
Citation
Ramírez-Acosta S, Arias-Borrego A, Navarro-Roldán F, et al. Omic methodologies for assessing metal(-loid)s-host-microbiota interplay: A review. Anal Chim Acta. 2021;1175:338620. doi:10.1016/j.aca.2021.338620
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