Exploratory multi-omics analysis reveals sex-specific differences in microbial response to antibiotic exposure
Antibiotic exposure is a major driver of microbiome disruption and antimicrobial resistance gene (ARG) expansion. Yet, the role of biological sex in shaping these responses remains poorly understood. Most studies do not stratify antibiotic-induced microbiome changes by sex or integrate multi-omics datasets, limiting our understanding of how microbial, metabolic, and immune responses interact.…
A recent study has revealed sex-specific differences in the microbial response to antibiotic exposure, shedding new light on the complex interactions between the gut microbiome, host metabolism, and immune system. Antibiotic usage is known to disrupt the microbiome and promote the expansion of antimicrobial resistance genes (ARGs), but the impact of biological sex on these responses has remained largely unexplored.
Most existing research has not accounted for sex differences nor integrated multi-omics datasets, which hinders a comprehensive understanding of the interplay between microbial, metabolic, and immune responses.
The current study aimed to address these limitations by conducting an exploratory analysis of continuous antibiotic exposure and its effects on the gut microbiome across different stages of sexual maturation. Male and female mice underwent antibiotic treatment for an extended period and were subsequently profiled using shotgun metagenomics, untargeted metabolomics, and bulk RNA sequencing of the spleen.
This integrative multi-omics framework allowed researchers to assess changes in microbial composition, ARG dynamics, metabolic profiles, and immune responses.
The results of this study demonstrated striking sex-specific correlations at a systems-level, providing valuable context to the observed differences in males and females upon antibiotic exposure. By integrating data from multiple layers of the host-microbiome system, this research highlights the critical need for a more comprehensive approach to understanding the impact of antibiotics on the human microbiome.
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