J Bacteriol Virol.  2017 Mar;47(1):64-74. 10.4167/jbv.2017.47.1.64.

The Effect of Probiotics, Antibiotics, and Antipyretic Analgesics on Gut Microbiota Modification

Affiliations
  • 1Department of Biochemistry, Ewha Medical Research Institute, School of Medicine, Ewha Womans University, Seoul, Korea. soyounwoo@ewha.ac.kr hyung@ewha.ac.kr
  • 2Center for Cohort Studies, Total Healthcare Center, Kangbuk Samsung Hospital, School of Medicine, Sungkyunkwan University, Seoul, Korea.
  • 3Department of Microbiology, Ewha Medical Research Institute, School of Medicine, Ewha Womans University, Seoul, Korea. soyounwoo@ewha.ac.kr hyung@ewha.ac.kr

Abstract

Human gut microbial community is playing a critical role in human health and associated with different human disease. In parallel, probiotics, antibiotics, and antipyretic analgesics (AAs) were developed to improve human health or cure human diseases. We therefore examined how probiotics, antibiotics, and AAs influence to the gut microbiota. Three independent case/control studies were designed from the cross-sectional cohort data of 1,463 healthy Koreans. The composition of the gut microbiota in each case and control group was determined via 16S ribosomal RNA Illumina next-generation sequencing. The correlation between microbial taxa and the consumption of each drug was tested using zero-inflated Gaussian mixture models, with covariate adjustment of age, sex, and body mass index (BMI). Probiotics, antibiotics, and AAs consumption yielded the significant differences in the gut microbiota, represented the lower abundance of Megasphaera in probiotics, the higher abundance of Fusobacteria in antibiotics, and the higher abundance of Butyrivibrio and Verrucomicrobia in AAs, compared to each control group. The reduction of Erysipelotrichaceae family was common in three drugs consumption.

Keyword

Gut microbiota; Probiotics; Antibiotics; Antipyretic analgesics

MeSH Terms

Analgesics*
Anti-Bacterial Agents*
Body Mass Index
Butyrivibrio
Cohort Studies
Fusobacteria
Gastrointestinal Microbiome*
Humans
Megasphaera
Probiotics*
RNA, Ribosomal, 16S
Verrucomicrobia
Analgesics
Anti-Bacterial Agents
RNA, Ribosomal, 16S

Figure

  • Figure 1. Comparison of gut microbiota between 14 probiotics and 28 control groups. (A) Alpha-diversity (Shannon index), (B) beta-diversity of PCoA plots in probiotics group by weighted UniFrac, (C) weighted UniFrac distance box plot within and between groups (∗∗ p < 0.01).

  • Figure 2. Comparison of gut microbiota between 55 antibiotics and 110 control groups. (A) Alpha-diversity (Shannon index), (B) beta-diversity of PCoA plots in antibiotics group by weighted UniFrac, (C) weighted UniFrac distance box plot within and between groups (∗p < 0.05).

  • Figure 3. Comparison of gut microbiota between 47 AAs and 94 control groups. (A) Alpha-diversity (Shannon index), (B) beta-diversity of PCoA plots in AAs group by weighted UniFrac, (C) weighted UniFrac distance box plot within and between groups (∗p < 0.05).


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