Abstract
Benzo[a]pyrene (B[a]P) is a ubiquitous, persistent, and carcinogenic pollutant that belongs to the large family of polycyclic aromatic hydrocarbons. Population exposure primarily occurs via contaminated food products, which introduces the pollutant to the digestive tract. Although the metabolism of B[a]P by host cells is well known, its impacts on the human gut microbiota, which plays a key role in health and disease, remain unexplored. We performed an in vitro assay using 16S barcoding, metatranscriptomics and volatile metabolomics to study the impact of B[a]P on two distinct human fecal microbiota. B[a]P exposure did not induce a significant change in the microbial structure; however, it altered the microbial volatolome in a dose-dependent manner. The transcript levels related to several metabolic pathways, such as vitamin and cofactor metabolism, cell wall compound metabolism, DNA repair and replication systems, and aromatic compound metabolism, were upregulated, whereas the transcript levels related to the glycolysis-gluconeogenesis pathway and bacterial chemotaxis toward simple carbohydrates were downregulated. These primary findings show that food pollutants, such as B[a]P, alter human gut microbiota activity. The observed shift in the volatolome demonstrates that B[a]P induces a specific deviation in the microbial metabolism.
Highlights
Polycyclic aromatic hydrocarbons (PAHs) are of great concern as environmental and foodborne pollutants
Two human fecal microbiota (FM) were exposed to three B[a]P concentrations (0.005, 0.05, and 0.5 mg/mL) for 24 h, and their structures were assessed via 16S rDNA/rRNA-based amplicon sequencing
The phylum Bacteroidetes is represented in both structures with the same relative abundance (60–65%), the microbial activity in fecal microbiota-1 (FM-1) and fecal microbiota-2 (FM-2) was dominated by the phyla Fusobacteria (28%) and Firmicutes (26.9%), respectively
Summary
Polycyclic aromatic hydrocarbons (PAHs) are of great concern as environmental and foodborne pollutants. Because of its mutagenic and carcinogenic effects in animal models Once in the GIT, B[a]P enters the entero-hepatic circulatory system and is metabolized by cytochrome P450-dependent monooxygenases present in intestinal enterocytes and liver hepatocytes, leading to the formation of diol-epoxide compounds. These toxic molecules subsequently form B[a]P-DNA adducts (DNA binding products) that have been previously characterized as necessary for B[a]P-initiated carcinogenesis (van Herwaarden et al, 2009)
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