Abstract
BACKGROUND: Early disruption of the microbial community may influence life-long health. Environmental toxicants can contaminate breast milk and the developing infant gut microbiome is directly exposed. We investigated whether environmental toxicants in breastmilk affect the composition and function of the infant gut microbiome at 1 month. We measured environmental toxicants in breastmilk, fecal short-chain fatty acids (SCFAs), and gut microbial composition from 16S rRNA gene amplicon sequencing using samples from 267 mother-child pairs in the Norwegian Microbiota Cohort (NoMIC). We tested 28 chemical exposures: polychlorinated biphenyls (PCBs), polybrominated flame retardants (PBDEs), per- and polyfluoroalkyl substances (PFASs), and organochlorine pesticides. We assessed chemical exposure and alpha diversity/SCFAs using elastic net regression modeling and generalized linear models, adjusting for confounders, and variation in beta diversity (UniFrac), taxa abundance (ANCOM), and predicted metagenomes (PiCRUSt) in low, medium, and high exposed groups.
RESULTS: PBDE-28 and the surfactant perfluorooctanesulfonic acid (PFOS) were associated with less microbiome diversity. Some sub-OTUs of Lactobacillus, an important genus in early life, were lower in abundance in samples from infants with relative "high" (> 80th percentile) vs. "low" (< 20th percentile) toxicant exposure in this cohort. Moreover, breast milk toxicants were associated with microbiome functionality, explaining up to 34% of variance in acetic and propionic SCFAs, essential signaling molecules. Per one standard deviation of exposure, PBDE-28 was associated with less propionic acid (- 24% [95% CI - 35% to - 14%] relative to the mean), and PCB-209 with less acetic acid (- 15% [95% CI - 29% to - 0.4%]). Conversely, PFOA and dioxin-like PCB-167 were associated with 61% (95% CI 35% to 87%) and 22% (95% CI 8% to 35%) more propionic and acetic acid, respectively.
CONCLUSIONS: Environmental toxicant exposure may influence infant gut microbial function during a critical developmental window. Future studies are needed to replicate these novel findings and investigate whether this has any impact on child health.
| Original language | English |
|---|---|
| Article number | 34 |
| Pages (from-to) | 34 |
| Journal | Microbiome |
| Volume | 7 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - 27 Feb 2019 |
Funding
In the interest of full disclosure of what may be perceived or potential competing financial interests, the authors R.K., A.G., and S.J. declare that they have been partially supported by a grant from the United States National Institute of Health R01 DK 110793-01 and the Gerber Foundation titled “Effects of Human Milk Oligosaccharides on the Developing Infant Gut Microbiome and Adiposity Changes in Early Infancy.” Furthermore, RK is on the Scientific Advisory Board for Commense Inc. Commense is pioneering a deep understanding of the microbiome early in life and its fundamental role in promoting a lifetime of health. Drawing insights from natural exposures to beneficial microbes, Commense is developing approaches to guide the priming, seeding and maintaining of the microbiome in infants and children. The remaining authors declare that they have no competing interests. This work was supported by the Norwegian Research Council grant agreements “Human Infant Gut Microbiota” No 214324/F20, and "NON-PROTECTED" No. 275903/F20.
| Funders | Funder number |
|---|---|
| National Institutes of Health | R01 DK 110793-01 |
| Gerber Foundation | |
| Norges forskningsråd | 214324/F20, 275903/F20 |
Keywords
- Adult
- Humans
- Infant, Newborn
- Bacteria/classification
- Biodiversity
- Cohort Studies
- DNA, Bacterial/genetics
- DNA, Ribosomal/genetics
- Environmental Pollutants/adverse effects
- Fatty Acids, Volatile/analysis
- Feces/chemistry
- Flame Retardants/adverse effects
- Gastrointestinal Microbiome/drug effects
- Hydrocarbons, Chlorinated/adverse effects
- Maternal Age
- Metabolomics
- Milk, Human/chemistry
- Norway
- Pesticides/adverse effects
- Polychlorinated Biphenyls/adverse effects
- RNA, Ribosomal, 16S/genetics
- Sequence Analysis, DNA/methods
- Female
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