Dietary regulation of the gut microbiota engineered by a minimal defined bacterial consortium

Ting Chin David Shen, Christel Chehoud, Josephine Ni, Evelyn Hsu, Ying Yu Chen, Aubrey Bailey, Alice Laughlin, Kyle Bittinger, Frederic D. Bushman, Gary D.Wu Wu

Research output: Contribution to journalArticlepeer-review

12 Scopus citations

Abstract

We have recently reported that Altered Schaedler Flora (ASF) can be used to durably engineer the gut microbiota to reduce ammonia production as an effective modality to reduce morbidity and mortality in the setting of liver injury. Here we investigated the effects of a low protein diet on ASF colonization and its ability to engineer the microbiota. Initially, ASF inoculation was similar between mice fed a normal protein diet or low protein diet, but the outgrowth of gut microbiota differed over the ensuing month. Notable was the inability of the dominant Parabacteroides ASF taxon to exclude other taxa belonging to the Bacteroidetes phylum in the setting of a low protein diet. Instead, a poorly classified yet highly represented Bacteroidetes family, S24-7, returned within 4 weeks of inoculation in mice fed a low protein diet, demonstrating a reduction in ASF resilience in response to dietary stress. Nevertheless, fecal ammonia levels remained significantly lower than those observed in mice on the same low protein diet that received a transplant of normal feces. No deleterious effects were observed in host physiology due to ASF inoculation into mice on a low protein diet. In total, these results demonstrate that low protein diet can have a pronounced effect on engineering the gut microbiota but modulation of ammonia is preserved.

Original languageEnglish (US)
Article numbere0155620
JournalPloS one
Volume11
Issue number5
DOIs
StatePublished - May 2016
Externally publishedYes

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)
  • Agricultural and Biological Sciences(all)
  • General

Fingerprint

Dive into the research topics of 'Dietary regulation of the gut microbiota engineered by a minimal defined bacterial consortium'. Together they form a unique fingerprint.

Cite this