The University of Southampton
University of Southampton Institutional Repository

Xylo-oligosaccharides alone or in synbiotic combination with Bifidobacterium animalis subsp. lactis induce bifidogenesis and modulate markers of immune function in healthy adults: a double-blind, placebo-controlled, randomised, factorial cross-over study

Xylo-oligosaccharides alone or in synbiotic combination with Bifidobacterium animalis subsp. lactis induce bifidogenesis and modulate markers of immune function in healthy adults: a double-blind, placebo-controlled, randomised, factorial cross-over study
Xylo-oligosaccharides alone or in synbiotic combination with Bifidobacterium animalis subsp. lactis induce bifidogenesis and modulate markers of immune function in healthy adults: a double-blind, placebo-controlled, randomised, factorial cross-over study
Prebiotics, probiotics and synbiotics are dietary ingredients with the potential to influence health and mucosal and systemic immune function by altering the composition of the gut microbiota. In the present study, a candidate prebiotic (xylo-oligosaccharide, XOS, 8 g/d), probiotic (Bifidobacterium animalis subsp. lactis Bi-07, 109 colony-forming units (CFU)/d) or synbiotic (8 g XOS+109 CFU Bi-07/d) was given to healthy adults (25–65 years) for 21 d. The aim was to identify the effect of the supplements on bowel habits, self-reported mood, composition of the gut microbiota, blood lipid concentrations and immune function. XOS supplementation increased mean bowel movements per d (P= 0·009), but did not alter the symptoms of bloating, abdominal pain or flatulence or the incidence of any reported adverse events compared with maltodextrin supplementation. XOS supplementation significantly increased participant-reported vitality (P= 0·003) and happiness (P= 0·034). Lowest reported use of analgesics was observed during the XOS+Bi-07 supplementation period (P= 0·004). XOS supplementation significantly increased faecal bifidobacterial counts (P= 0·008) and fasting plasma HDL concentrations (P= 0·005). Bi-07 supplementation significantly increased faecal B. lactis content (P= 0·007), lowered lipopolysaccharide-stimulated IL-4 secretion in whole-blood cultures (P= 0·035) and salivary IgA content (P= 0·040) and increased IL-6 secretion (P= 0·009). XOS supplementation resulted in lower expression of CD16/56 on natural killer T cells (P= 0·027) and lower IL-10 secretion (P= 0·049), while XOS and Bi-07 supplementation reduced the expression of CD19 on B cells (XOS × Bi-07, P= 0·009). The present study demonstrates that XOS induce bifidogenesis, improve aspects of the plasma lipid profile and modulate the markers of immune function in healthy adults. The provision of XOS+Bi-07 as a synbiotic may confer further benefits due to the discrete effects of Bi-07 on the gut microbiota and markers of immune function.
0007-1145
1945-1956
Childs, Caroline
ea17ccc1-2eac-4f67-96c7-a0c4d9dfd9c5
Röytiö, Henna
cabbeb44-0c2f-4d04-a3b7-fc80fbd4fa35
Alhoniemi, Esa
90712cc8-4f62-4982-a797-cd55dc9052b2
Fekete, Agnes A.
e09ec361-455c-497b-a8f8-d3dbccb5ff69
Forssten, Sofia D.
95b35eb9-def7-4f5f-819c-e8c843368eb3
Hudjec, Natasa
322e6502-e558-46bc-b33f-9682c1a1da9b
Lim, Ying Ni
70116380-6472-4333-9807-85b147a26459
Steger, Cara J.
205522c8-7983-4953-8a13-430f9251332b
Yaqoob, Parveen
3a418e24-bbf0-4b31-9df8-ca8514885c82
Tuohy, Kieran M.
33a7a5da-4abd-4759-b992-2cd45fc65831
Rastall, Robert A.
c8c930d7-f2d4-4af6-adf2-ed71e8b1992f
Ouwehand, Arthur C.
b3fdeef6-9ce4-4311-88a7-46fdfcd7a4d3
Gibson, Glenn R.
24ac4753-4f78-475f-9766-5da179e2ab92
Childs, Caroline
ea17ccc1-2eac-4f67-96c7-a0c4d9dfd9c5
Röytiö, Henna
cabbeb44-0c2f-4d04-a3b7-fc80fbd4fa35
Alhoniemi, Esa
90712cc8-4f62-4982-a797-cd55dc9052b2
Fekete, Agnes A.
e09ec361-455c-497b-a8f8-d3dbccb5ff69
Forssten, Sofia D.
95b35eb9-def7-4f5f-819c-e8c843368eb3
Hudjec, Natasa
322e6502-e558-46bc-b33f-9682c1a1da9b
Lim, Ying Ni
70116380-6472-4333-9807-85b147a26459
Steger, Cara J.
205522c8-7983-4953-8a13-430f9251332b
Yaqoob, Parveen
3a418e24-bbf0-4b31-9df8-ca8514885c82
Tuohy, Kieran M.
33a7a5da-4abd-4759-b992-2cd45fc65831
Rastall, Robert A.
c8c930d7-f2d4-4af6-adf2-ed71e8b1992f
Ouwehand, Arthur C.
b3fdeef6-9ce4-4311-88a7-46fdfcd7a4d3
Gibson, Glenn R.
24ac4753-4f78-475f-9766-5da179e2ab92

Childs, Caroline, Röytiö, Henna, Alhoniemi, Esa, Fekete, Agnes A., Forssten, Sofia D., Hudjec, Natasa, Lim, Ying Ni, Steger, Cara J., Yaqoob, Parveen, Tuohy, Kieran M., Rastall, Robert A., Ouwehand, Arthur C. and Gibson, Glenn R. (2014) Xylo-oligosaccharides alone or in synbiotic combination with Bifidobacterium animalis subsp. lactis induce bifidogenesis and modulate markers of immune function in healthy adults: a double-blind, placebo-controlled, randomised, factorial cross-over study. British Journal of Nutrition, 111 (11), 1945-1956. (doi:10.1017/S0007114513004261).

Record type: Article

Abstract

Prebiotics, probiotics and synbiotics are dietary ingredients with the potential to influence health and mucosal and systemic immune function by altering the composition of the gut microbiota. In the present study, a candidate prebiotic (xylo-oligosaccharide, XOS, 8 g/d), probiotic (Bifidobacterium animalis subsp. lactis Bi-07, 109 colony-forming units (CFU)/d) or synbiotic (8 g XOS+109 CFU Bi-07/d) was given to healthy adults (25–65 years) for 21 d. The aim was to identify the effect of the supplements on bowel habits, self-reported mood, composition of the gut microbiota, blood lipid concentrations and immune function. XOS supplementation increased mean bowel movements per d (P= 0·009), but did not alter the symptoms of bloating, abdominal pain or flatulence or the incidence of any reported adverse events compared with maltodextrin supplementation. XOS supplementation significantly increased participant-reported vitality (P= 0·003) and happiness (P= 0·034). Lowest reported use of analgesics was observed during the XOS+Bi-07 supplementation period (P= 0·004). XOS supplementation significantly increased faecal bifidobacterial counts (P= 0·008) and fasting plasma HDL concentrations (P= 0·005). Bi-07 supplementation significantly increased faecal B. lactis content (P= 0·007), lowered lipopolysaccharide-stimulated IL-4 secretion in whole-blood cultures (P= 0·035) and salivary IgA content (P= 0·040) and increased IL-6 secretion (P= 0·009). XOS supplementation resulted in lower expression of CD16/56 on natural killer T cells (P= 0·027) and lower IL-10 secretion (P= 0·049), while XOS and Bi-07 supplementation reduced the expression of CD19 on B cells (XOS × Bi-07, P= 0·009). The present study demonstrates that XOS induce bifidogenesis, improve aspects of the plasma lipid profile and modulate the markers of immune function in healthy adults. The provision of XOS+Bi-07 as a synbiotic may confer further benefits due to the discrete effects of Bi-07 on the gut microbiota and markers of immune function.

Text
Childs CE _ XOS.docx - Accepted Manuscript
Download (74kB)

More information

Submitted date: 12 April 2013
Accepted/In Press date: 29 November 2013
e-pub ahead of print date: 24 March 2014
Published date: 24 March 2014
Organisations: Faculty of Medicine, Human Development & Health

Identifiers

Local EPrints ID: 394848
URI: http://eprints.soton.ac.uk/id/eprint/394848
ISSN: 0007-1145
PURE UUID: 592d74d8-39c6-4f94-b40b-304b5dc444c5
ORCID for Caroline Childs: ORCID iD orcid.org/0000-0001-6832-224X

Catalogue record

Date deposited: 24 May 2016 15:36
Last modified: 15 Mar 2024 03:31

Export record

Altmetrics

Contributors

Author: Caroline Childs ORCID iD
Author: Henna Röytiö
Author: Esa Alhoniemi
Author: Agnes A. Fekete
Author: Sofia D. Forssten
Author: Natasa Hudjec
Author: Ying Ni Lim
Author: Cara J. Steger
Author: Parveen Yaqoob
Author: Kieran M. Tuohy
Author: Robert A. Rastall
Author: Arthur C. Ouwehand
Author: Glenn R. Gibson

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×