# Short-term exposure to antibiotics begets long-term disturbance in gut microbial metabolism and molecular ecological networks

**Authors:** Yuehui Hong, Hao Li, Linkang Chen, Hongtian Su, Bin Zhang, Yu Luo, Chengji Li, Zuguo Zhao, Yiming Shao, Lianxian Guo

PMC · DOI: 10.1186/s40168-024-01795-z · Microbiome · 2024-05-07

## TL;DR

Short-term antibiotic exposure in early life can lead to long-term changes in gut microbes and their networks in mice.

## Contribution

The study reveals long-term disturbances in gut microbial diversity, metabolism, and network complexity following brief early-life antibiotic exposure.

## Key findings

- Short-term ceftriaxone exposure reduced gut microbial diversity, which partially recovered but did not return to baseline.
- Antibiotic exposure disrupted gut molecular ecological networks, reducing complexity and key species.
- Metabolic profiles differed significantly between antibiotic-treated and control groups, linked to network changes.

## Abstract

Antibiotic exposure can occur in medical settings and from environmental sources. Long-term effects of brief antibiotic exposure in early life are largely unknown.

Post a short-term treatment by ceftriaxone to C57BL/6 mice in early life, a 14-month observation was performed using 16S rRNA gene-sequencing technique, metabolomics analysis, and metagenomics analysis on the effects of ceftriaxone exposure. Firstly, the results showed that antibiotic pre-treatment significantly disturbed gut microbial α and β diversities (P < 0.05). Both Chao1 indices and Shannon indices manifested recovery trends over time, but they didn’t entirely recover to the baseline of control throughout the experiment. Secondly, antibiotic pre-treatment reduced the complexity of gut molecular ecological networks (MENs). Various network parameters were affected and manifested recovery trends over time with different degrees, such as nodes (P < 0.001, R2 = 0.6563), links (P < 0.01, R2 = 0.4543), number of modules (P = 0.0672, R2 = 0.2523), relative modularity (P = 0.6714, R2 = 0.0155), number of keystones (P = 0.1003, R2 = 0.2090), robustness_random (P = 0.79, R2 = 0.0063), and vulnerability (P = 0.0528, R2 = 0.28). The network parameters didn't entirely recover. Antibiotic exposure obviously reduced the number of key species in gut MENs. Interestingly, new keystones appeared during the recovery process of network complexity. Changes in network stability might be caused by variations in network complexity, which supports the ecological theory that complexity begets stability. Besides, the metabolism profiles of the antibiotic group and control were significantly different. Correlation analysis showed that antibiotic-induced differences in gut microbial metabolism were related to MEN changes. Antibiotic exposure also caused long-term effects on gut microbial functional networks in mice.

These results suggest that short-term antibiotic exposure in early life will cause long-term negative impacts on gut microbial diversity, MENs, and microbial metabolism. Therefore, great concern should be raised about children’s brief exposure to antibiotics if the results observed in mice are applicable to humans.

Video Abstract

Video Abstract

The online version contains supplementary material available at 10.1186/s40168-024-01795-z.

## Linked entities

- **Chemicals:** ceftriaxone (PubChem CID 5479530)

## Full-text entities

- **Chemicals:** ceftriaxone (MESH:D002443)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** C57BL/6 — Mus musculus (Mouse), Transformed cell line (CVCL_C0MU)

## Full text

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## Figures

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## References

68 references — full list in the complete paper: https://tomesphere.com/paper/PMC11075301/full.md

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Source: https://tomesphere.com/paper/PMC11075301