Hostname: page-component-586b7cd67f-rcrh6 Total loading time: 0 Render date: 2024-11-26T05:41:05.498Z Has data issue: false hasContentIssue false

Fermentation of oats (Avena sativa) by the faecal microbiota using an in vitro colonic fermentor system

Published online by Cambridge University Press:  23 September 2015

A.J. Chappell
Affiliation:
Rowett Institute of Nutrition and Health, University of Aberdeen, Aberdeen, AB25 9SB
F. Thies
Affiliation:
Rowett Institute of Nutrition and Health, University of Aberdeen, Aberdeen, AB25 9SB
P. Martin
Affiliation:
Agronomy Institute, Orkney College, University of the Highlands and Islands, Orkney, KW15 1LX
H.J. Flint
Affiliation:
Rowett Institute of Nutrition and Health, University of Aberdeen, Aberdeen, AB25 9SB
K.P. Scott
Affiliation:
Rowett Institute of Nutrition and Health, University of Aberdeen, Aberdeen, AB25 9SB
Rights & Permissions [Opens in a new window]

Abstract

Type
Abstract
Copyright
Copyright © The Authors 2015 

Diets high in whole grain cereals may reduce the risk of cardiovascular disease and colorectal cancerReference Hotchkiss, Davies. and Gray 1 Reference Eshak, Iso and Date. 2 . The mixed link β-glucans found within oats (Avena sativa) could be partly responsible for this. The cholesterol lowering effect of β-glucans are well documented and currently has several endorsed health claims 3 4 . Little is known about how oat consumption influences the gut microbiota. The development of culture independent techniques using 16S rRNA-targeting arrays have demonstrated the importance of bacterial community composition, and bacterial metabolites, in health and disease. Prebiotics, non-digestible plant derived carbohydrates, act as fermentation substrates stimulating preferential growth and activity of potentially beneficial microbes. In vitro models may provide a useful insight into how these substrates might influence microbial composition in vivo Reference Kellow, Coughlan and Reid 5 .

Here we investigated the effects of a pre-digested oat sample on microbial activity and composition using a continuous flow anaerobic fermentor model with both a luminal and mucosal environment. Firstly the oat sample underwent a pre-digestion with stomach and intestinal enzymes to reduce starch, free sugars, protein, and fat content. Fermentors were then inoculated with faecal samples obtained from four different volunteers and then run for 98 h on a growth medium before switching to oats. Fermentors were run for a total of 264 h including the initial 98 h growth phase, at pH 5·8 and 6·5 with half the mucosal environment replaced daily. An additional fermentor was run using the initial growth medium as a comparison. Samples were taken daily for short chain fatty acids (SCFA) and at 0, 98, 168, and 264 h for microbial composition analysis of both the luminal and mucosal environment.

An analysis within volunteers comparing oats pH 6·5, and 5·8 to growth pH 6·5 was performed using an ANOVA. Total SCFA analysis indicated the oats were more fermentable at pH 6·5 compared to pH 5·8 (p < 0·05), and that acetate was the most abundant SCFA followed by propionate. Fermentation was significantly higher with the growth medium compared to TDS (p < 0·05).

Fermentor Short Chain Fatty Acids at 264 h

Growth was a carbohydrate rich mixed medium

Different letters within columns denote significant difference (p < 0·05).

Microbial analysis of the oat fermentors by fluorescence in situ hybridisation found a shift towards the Bacteroides genus in the luminal compared to the mucosal environment. Eubacterium rectale, Lactobacillus and Desulfovibrio group all had a preference for the mucosal environment (p < 0·05). A trend was also noted indicating the Atopobium may have a preference for the growth medium compared to the oats (p = 0·08). The total bacterial counts were greater for the control and oats at pH 6·5 compared to oats pH 5·8, indicative of the challenging growth conditions (p < 0·05). Bias towards the Bacteroides groups in fermentor experiments has been reported previouslyReference Abbeele 6 , incorporation of the mucosal environment into our model reduced this bias. Further refinement of the model however maybe required to identify microbes that ferment oat fibre in vitro.

References

1. Hotchkiss, JW, Davies., C, Gray, L, et al. (2011) BMJ 1(1), 114.Google Scholar
2. Eshak, ES, Iso, H, Date., C, et al. (2010) J Nutr 140, 14451453.Google Scholar
3. EFSA Panel on Dietetic Products, Nutrition and Allergies. (2011) EFSA J 9, 2207.Google Scholar
4. U.S FDA. (1997) Fed Regist 62, 35843681.Google Scholar
5. Kellow, NJ, Coughlan, MT, Reid, CM, (2014) BJN 111, 11471161.CrossRefGoogle Scholar
6. Abbeele, VP, et al. (2013). ISME l, 949961.CrossRefGoogle Scholar