2013
DOI: 10.1016/j.mimet.2013.08.008
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Evaluation of microbial community reproducibility, stability and composition in a human distal gut chemostat model

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Cited by 155 publications
(176 citation statements)
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“…The De-stat culture has not been applied for studies of complex microbial consortia earlier, while chemostat gut models have been used by several groups. It has been shown that major shifts in variability of fecal microbiota take place within the first 3–4 residential times while slight fluctuations occur even after 30 residential times [13,20,30] because of complex nature of the microbiota. Hence, the De-stat presented in the current paper is a promising approach for analyzing of the growth rate in microbial consortia with potential impact on health.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…The De-stat culture has not been applied for studies of complex microbial consortia earlier, while chemostat gut models have been used by several groups. It has been shown that major shifts in variability of fecal microbiota take place within the first 3–4 residential times while slight fluctuations occur even after 30 residential times [13,20,30] because of complex nature of the microbiota. Hence, the De-stat presented in the current paper is a promising approach for analyzing of the growth rate in microbial consortia with potential impact on health.…”
Section: Discussionmentioning
confidence: 99%
“…In vitro models facilitate frequent sampling and increased reproducibility [13]. Despite clear associations between the colonic transit time and microbiota, the effect of specific growth rate on the composition and metabolism of microbiota is not studied thoroughly in vitro .…”
Section: Introductionmentioning
confidence: 99%
“…In vitro systems allow for even more control of microbial communities but come with the downside that the contributions of the host to ecosystem parameters can only be measured superficially (e.g., by the addition of host proteins, such as mucins; Allen-Vercoe 2013;McDonald et al 2013). Culturing microbes from the mammalian gut can be challenging because many are fastidious in their nutritional needs and require cooperation with other species for optimal growth (Allen-Vercoe 2013).…”
Section: Experimental Tests Of Microbiome Invasibilitymentioning
confidence: 99%
“…The vessel was run in batch with pH control for 1 day prior to running under flow conditions (media fed at a rate of 400 mL/day) to give a retention time of 24 hours. Steady-state, as assessed through the amplification of 16S rRNA gene sequences using polymerase chain reaction (PCR) and denaturing gradient gel electrophoresis (DGGE-PCR) with moving window analysis [32,33], was attained by 7 days following chemostat operation. At steady-state, samples were aseptically removed from the vessel into a Ruskin anaerobic chamber (The Baker Co., USA) with a gas composition of 80% N 2 , 10% CO 2 , and 10% H 2 and used within ~3 h for further experiments.…”
Section: Human Gut Ecosystemmentioning
confidence: 99%