Metagenomics analysis of mice gut microbiome to unravel the role of metal exposure and piperine.
Ravidarshdeep KaurDhirendra Pratap SinghRakesh M RawalPublished in: Access microbiology (2024)
The gut and intestinal microbiota consists of trillions of microorganisms inhabiting the human gastrointestinal tract. It plays a crucial role in human health leading to understanding the dynamic crosstalk of host-microbe interaction in the gut and has become necessary for the detection, prevention, or therapy of diseases. Gut microbiota deviations are linked with many diseases, suggesting that various pathways involved in immunity, energy, lipid, and glucose metabolism are affected. Further, it is also altered by external insults such as metal toxicity, antibiotics and pesticides. Heavy metals like arsenic, mercury, cadmium and chromium are some of the well-studied classes of environmental pollutants. Mouse models have become the model of choice for most studies in this emerging field, as they allow perturbations in the gut microbiota to be studied in a controlled experimental setup. Here, we investigate the composition and diversity of intestinal microbes utilizing cecal samples from different intervention groups: arsenic exposure (As(III)), arsenic and piperine co-administration (As +Pp), piperine per se and control group. We obtained DNA samples from these groups and performed PCR amplification and sequencing of the 16S V3-V4 region. The findings showed shift in microbial composition and abundance among different intervention groups, revealing taxa that may contribute to the microbial diversity.
Keyphrases
- heavy metals
- risk assessment
- human health
- health risk assessment
- randomized controlled trial
- health risk
- microbial community
- endothelial cells
- sewage sludge
- drinking water
- mouse model
- real time pcr
- nucleic acid
- circulating tumor
- climate change
- label free
- antibiotic resistance genes
- loop mediated isothermal amplification
- single molecule
- solid state
- metabolic syndrome
- fatty acid
- stem cells
- induced pluripotent stem cells
- adipose tissue
- type diabetes
- mass spectrometry
- sensitive detection
- liquid chromatography
- replacement therapy