4.7 Article

Prebiotics Modulate the Effects of Antibiotics on Gut Microbial Diversity and Functioning in Vitro

Journal

NUTRIENTS
Volume 7, Issue 6, Pages 4480-4497

Publisher

MDPI
DOI: 10.3390/nu7064480

Keywords

gut microbiota; antibiotics; prebiotics; fibre

Funding

  1. National Centre for the Replacement, Refinement and Reduction of Animals in Research (NC3Rs)
  2. NC3R Ph.D. studentship
  3. BBSRC [BB/H004971/1, BB/L004259/1] Funding Source: UKRI
  4. Biotechnology and Biological Sciences Research Council [BB/H004971/1, BB/L004259/1, 1527476] Funding Source: researchfish
  5. National Centre for the Replacement, Refinement and Reduction of Animals in Research (NC3Rs) [NC/K50029X/1] Funding Source: researchfish
  6. National Institute for Health Research [NF-SI-0513-10029] Funding Source: researchfish

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Intestinal bacteria carry out many fundamental roles, such as the fermentation of non-digestible dietary carbohydrates to produce short chain fatty acids (SCFAs), which can affect host energy levels and gut hormone regulation. Understanding how to manage this ecosystem to improve human health is an important but challenging goal. Antibiotics are the front line of defence against pathogens, but in turn they have adverse effects on indigenous microbial diversity and function. Here, we have investigated whether dietary supplementationanother method used to modulate gut composition and functioncould be used to ameliorate the side effects of antibiotics. We perturbed gut bacterial communities with gentamicin and ampicillin in anaerobic batch cultures in vitro. Cultures were supplemented with either pectin (a non-fermentable fibre), inulin (a commonly used prebiotic that promotes the growth of beneficial bacteria) or neither. Although antibiotics often negated the beneficial effects of dietary supplementation, in some treatment combinations, notably ampicillin and inulin, dietary supplementation ameliorated the effects of antibiotics. There is therefore potential for using supplements to lessen the adverse effects of antibiotics. Further knowledge of such mechanisms could lead to better therapeutic manipulation of the human gut microbiota.

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