Influence of cultivation ph on composition, diversity, and metabolic production in an in vitro human intestinal microbiota

Regina Haindl, Simon Schick, Ulrich Kulozik

Research output: Contribution to journalArticlepeer-review

8 Scopus citations

Abstract

Fecal microbiota transplantation, an alternative treatment method for gastrointestinal diseases, has a high recovery rate, but comes with disadvantages, such as high donor requirements and the low storability of stool. A solution to overcome these problems is the cultivation of an in vitro microbiota. However, the influence of cultivation conditions on the pH are yet unknown. In this study, the influence of the cultivation pH (6.0–7.0) on the system’s behavior and characteristics, including cell count, metabolism, and microbial composition, was investigated. With an increasing cultivation pH, an increase in cell count, total amount of SCFAs, acetate, propionate, and the abundance of Bacteroidetes and Verrucomicrobia were observed. For the concentration of butyrate and the abundance of Actinobacteria and Firmicutes, a decrease with increasing pH was determined. For the concentration of isovalerate, the abundance of Proteobacteria and diversity (richness and Shannon effective), no effect of the pH was observed. Health-promoting genera were more abundant at lower pH levels. When cultivating an in vitro microbiota, all investigated pH values created a diverse and stable system. Ultimately, therefore, the choice of pH creates significant differences in the established in vitro microbiota, but no clear recommendations for a special value can be made.

Original languageEnglish
Article number156
JournalFermentation
Volume7
Issue number3
DOIs
StatePublished - Sep 2021

Keywords

  • 16S rRNA sequencing
  • Continuous flow fermentation
  • Diversity
  • PH 6.0
  • PH 6.5
  • PH 7.0
  • Richness
  • Shannon effective index
  • Short-chain fatty acids

Fingerprint

Dive into the research topics of 'Influence of cultivation ph on composition, diversity, and metabolic production in an in vitro human intestinal microbiota'. Together they form a unique fingerprint.

Cite this