The effect of a multi-strain probiotic on the resistance toward Escherichia coli challenge in a randomized, placebo-controlled, double-blind intervention study

Background: Several probiotic strains have been shown to enhance human resistance to infectious disease. It is speculated that these strains may impose this effect by excretion of anti-microbial components, by competing with pathogens for intestinal nutrients and/or mucosal adhesion sites or modulat...

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Published inEuropean journal of clinical nutrition Vol. 69; no. 3; pp. 385 - 391
Main Authors Ten Bruggencate, S J M, Girard, S A, Floris-Vollenbroek, E G M, Bhardwaj, R, Tompkins, T A
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 01.03.2015
Nature Publishing Group
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Online AccessGet full text
ISSN0954-3007
1476-5640
1476-5640
DOI10.1038/ejcn.2014.238

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Abstract Background: Several probiotic strains have been shown to enhance human resistance to infectious disease. It is speculated that these strains may impose this effect by excretion of anti-microbial components, by competing with pathogens for intestinal nutrients and/or mucosal adhesion sites or modulating the immune system. Objective: A parallel, double-blind, placebo-controlled 4-week intervention was performed in healthy males, to study the effect of a blend of probiotic bacteria ( Lactobacillus helveticus Rosell-52 , Lactobacillus rhamnosus Rosell-11 , Bifidobacterium longum ssp. longum Rosell-175) and a probiotic yeast ( Saccharomyces cerevisiae var boulardii CNCM I-1079) on enterotoxigenic Escherichia coli (ETEC) challenge. Primary outcomes studied were fecal ETEC excretion and total fecal output per day. Subjects/Methods: Subjects were randomized to the probiotic (5 × 10 9 colony-forming units (CFUs); twice daily; n =30) or placebo group (twice daily; n =30). After 2 weeks, subjects were orally challenged with a live attenuated ETEC (3 × 10 9 CFU), previously demonstrated to induce mild, short-lived symptoms of a foodborne infection. Before and after ETEC challenge, subjects collected 24 h fecal samples. Compliance to study guidelines, stool consistency (Bristol Stool Score), stool frequency, and frequency and severity of gastrointestinal (GI) complaints were recorded by the subjects on a Daily Record Questionnaire. Results: ETEC challenge induced a significant increase in fecal ETEC excretion in both groups. However, a statistically significant increase in fecal output was only observed in the probiotic group. ETEC challenge resulted in a decrease in the percentage of fecal dry weight, and an increase in reported Bristol Stool Score, stool frequency and GI complaints. Dietary probiotics significantly decreased the percentage of fecal dry weight. In addition, ETEC increased C-reactive protein, total secretory Immunoglobulin A (IgA) and Immunoglobulin G Colonization Factor Antigen II. Conclusion: Dietary probiotics did not increase resistance to oral attenuated ETEC challenge in human subjects.
AbstractList BACKGROUND: Several probiotic strains have been shown to enhance human resistance to infectious disease. It is speculated that these strains may impose this effect by excretion of anti-microbial components, by competing with pathogens for intestinal nutrients and/or mucosal adhesion sites or modulating the immune system. OBJECTIVE: A parallel, double-blind, placebo-controlled 4-week intervention was performed in healthy males, to study the effect of a blend of probiotic bacteria (Lactobacillus helveticus Rosell-52, Lactobacillus rhamnosus Rosell-11, Bifidobacterium longum ssp. longum Rosell-175) and a probiotic yeast (Saccharomyces cerevisiae var boulardii CNCM I- 1079) on enterotoxigenic Escherichia coli (ETEC) challenge. Primary outcomes studied were fecal ETEC excretion and total fecal output per day. SUBJECTS/METHODS: Subjects were randomized to the probiotic (5 x [10.sup.9] colony-forming units (CFUs);twice daily;n = 30) or placebo group (twice daily; n = 30). After 2 weeks, subjects were orally challenged with a live attenuated ETEC (3 x [10.sup.9] CFU), previously demonstrated to induce mild, short-lived symptoms of a foodborne infection. Before and after ETEC challenge, subjects collected 24 h fecal samples. Compliance to study guidelines, stool consistency (Bristol Stool Score), stool frequency, and frequency and severity of gastrointestinal (GI) complaints were recorded by the subjects on a Daily Record Questionnaire. RESULTS: ETEC challenge induced a significant increase in fecal ETEC excretion in both groups. However, a statistically significant increase in fecal output was only observed in the probiotic group. ETEC challenge resulted in a decrease in the percentage of fecal dry weight, and an increase in reported Bristol Stool Score, stool frequency and GI complaints. Dietary probiotics significantly decreased the percentage of fecal dry weight. In addition, ETEC increased C-reactive protein, total secretory Immunoglobulin A (IgA) and Immunoglobulin G Colonization Factor Antigen II. CONCLUSION: Dietary probiotics did not increase resistance to oral attenuated ETEC challenge in human subjects. European Journal of Clinical Nutrition (2015) 69, 385-391; doi: 10.1038/ejcn.2014.238; published online 5 November 2014
Background:Several probiotic strains have been shown to enhance human resistance to infectious disease. It is speculated that these strains may impose this effect by excretion of anti-microbial components, by competing with pathogens for intestinal nutrients and/or mucosal adhesion sites or modulating the immune system.Objective:A parallel, double-blind, placebo-controlled 4-week intervention was performed in healthy males, to study the effect of a blend of probiotic bacteria (Lactobacillus helveticus Rosell-52, Lactobacillus rhamnosus Rosell-11, Bifidobacterium longum ssp. longum Rosell-175) and a probiotic yeast (Saccharomyces cerevisiae var boulardii CNCM I-1079) on enterotoxigenic Escherichia coli (ETEC) challenge. Primary outcomes studied were fecal ETEC excretion and total fecal output per day.Subjects/Methods:Subjects were randomized to the probiotic (5 × 109 colony-forming units (CFUs); twice daily; n=30) or placebo group (twice daily; n=30). After 2 weeks, subjects were orally challenged with a live attenuated ETEC (3 × 109 CFU), previously demonstrated to induce mild, short-lived symptoms of a foodborne infection. Before and after ETEC challenge, subjects collected 24 h fecal samples. Compliance to study guidelines, stool consistency (Bristol Stool Score), stool frequency, and frequency and severity of gastrointestinal (GI) complaints were recorded by the subjects on a Daily Record Questionnaire.Results:ETEC challenge induced a significant increase in fecal ETEC excretion in both groups. However, a statistically significant increase in fecal output was only observed in the probiotic group. ETEC challenge resulted in a decrease in the percentage of fecal dry weight, and an increase in reported Bristol Stool Score, stool frequency and GI complaints. Dietary probiotics significantly decreased the percentage of fecal dry weight. In addition, ETEC increased C-reactive protein, total secretory Immunoglobulin A (IgA) and Immunoglobulin G Colonization Factor Antigen II.Conclusion:Dietary probiotics did not increase resistance to oral attenuated ETEC challenge in human subjects.
BACKGROUND: Several probiotic strains have been shown to enhance human resistance to infectious disease. It is speculated that these strains may impose this effect by excretion of anti-microbial components, by competing with pathogens for intestinal nutrients and/or mucosal adhesion sites or modulating the immune system. OBJECTIVE: A parallel, double-blind, placebo-controlled 4-week intervention was performed in healthy males, to study the effect of a blend of probiotic bacteria (Lactobacillus helveticus Rosell-52, Lactobacillus rhamnosus Rosell-11, Bidobacterium longum ssp. longum Rosell-175) and a probiotic yeast (Saccharomyces cerevisiae var boulardii CNCM I-1079) on enterotoxigenic Escherichia coli (ETEC) challenge. Primary outcomes studied were fecal ETEC excretion and total fecal output per day. SUBJECTS/METHODS: Subjects were randomized to the probiotic (5 109 colony-forming units (CFUs); twice daily; n = 30) or placebo group (twice daily; n = 30). After 2 weeks, subjects were orally challenged with a live attenuated ETEC (3 109 CFU), previously demonstrated to induce mild, short-lived symptoms of a foodborne infection. Before and after ETEC challenge, subjects collected 24 h fecal samples. Compliance to study guidelines, stool consistency (Bristol Stool Score), stool frequency, and frequency and severity of gastrointestinal (GI) complaints were recorded by the subjects on a Daily Record Questionnaire. RESULTS: ETEC challenge induced a significant increase in fecal ETEC excretion in both groups. However, a statistically significant increase in fecal output was only observed in the probiotic group. ETEC challenge resulted in a decrease in the percentage of fecal dry weight, and an increase in reported Bristol Stool Score, stool frequency and GI complaints. Dietary probiotics significantly decreased the percentage of fecal dry weight. In addition, ETEC increased C-reactive protein, total secretory Immunoglobulin A (IgA) and Immunoglobulin G Colonization Factor Antigen II.
SUBJECTS/METHODS: Subjects were randomized to the probiotic (5 x [10.sup.9] colony-forming units (CFUs);twice daily;n = 30) or placebo group (twice daily; n = 30). After 2 weeks, subjects were orally challenged with a live attenuated ETEC (3 x [10.sup.9] CFU), previously demonstrated to induce mild, short-lived symptoms of a foodborne infection. Before and after ETEC challenge, subjects collected 24 h fecal samples. Compliance to study guidelines, stool consistency (Bristol Stool Score), stool frequency, and frequency and severity of gastrointestinal (GI) complaints were recorded by the subjects on a Daily Record Questionnaire. European Journal of Clinical Nutrition (2015) 69, 385-391; doi: 10.1038/ejcn.2014.238; published online 5 November 2014
Several probiotic strains have been shown to enhance human resistance to infectious disease. It is speculated that these strains may impose this effect by excretion of anti-microbial components, by competing with pathogens for intestinal nutrients and/or mucosal adhesion sites or modulating the immune system. A parallel, double-blind, placebo-controlled 4-week intervention was performed in healthy males, to study the effect of a blend of probiotic bacteria (Lactobacillus helveticus Rosell-52, Lactobacillus rhamnosus Rosell-11, Bifidobacterium longum ssp. longum Rosell-175) and a probiotic yeast (Saccharomyces cerevisiae var boulardii CNCM I-1079) on enterotoxigenic Escherichia coli (ETEC) challenge. Primary outcomes studied were fecal ETEC excretion and total fecal output per day. Subjects were randomized to the probiotic (5 × 10(9) colony-forming units (CFUs); twice daily; n=30) or placebo group (twice daily; n=30). After 2 weeks, subjects were orally challenged with a live attenuated ETEC (3 × 10(9) CFU), previously demonstrated to induce mild, short-lived symptoms of a foodborne infection. Before and after ETEC challenge, subjects collected 24 h fecal samples. Compliance to study guidelines, stool consistency (Bristol Stool Score), stool frequency, and frequency and severity of gastrointestinal (GI) complaints were recorded by the subjects on a Daily Record Questionnaire. ETEC challenge induced a significant increase in fecal ETEC excretion in both groups. However, a statistically significant increase in fecal output was only observed in the probiotic group. ETEC challenge resulted in a decrease in the percentage of fecal dry weight, and an increase in reported Bristol Stool Score, stool frequency and GI complaints. Dietary probiotics significantly decreased the percentage of fecal dry weight. In addition, ETEC increased C-reactive protein, total secretory Immunoglobulin A (IgA) and Immunoglobulin G Colonization Factor Antigen II. Dietary probiotics did not increase resistance to oral attenuated ETEC challenge in human subjects.
Background: Several probiotic strains have been shown to enhance human resistance to infectious disease. It is speculated that these strains may impose this effect by excretion of anti-microbial components, by competing with pathogens for intestinal nutrients and/or mucosal adhesion sites or modulating the immune system. Objective: A parallel, double-blind, placebo-controlled 4-week intervention was performed in healthy males, to study the effect of a blend of probiotic bacteria ( Lactobacillus helveticus Rosell-52 , Lactobacillus rhamnosus Rosell-11 , Bifidobacterium longum ssp. longum Rosell-175) and a probiotic yeast ( Saccharomyces cerevisiae var boulardii CNCM I-1079) on enterotoxigenic Escherichia coli (ETEC) challenge. Primary outcomes studied were fecal ETEC excretion and total fecal output per day. Subjects/Methods: Subjects were randomized to the probiotic (5 × 10 9 colony-forming units (CFUs); twice daily; n =30) or placebo group (twice daily; n =30). After 2 weeks, subjects were orally challenged with a live attenuated ETEC (3 × 10 9 CFU), previously demonstrated to induce mild, short-lived symptoms of a foodborne infection. Before and after ETEC challenge, subjects collected 24 h fecal samples. Compliance to study guidelines, stool consistency (Bristol Stool Score), stool frequency, and frequency and severity of gastrointestinal (GI) complaints were recorded by the subjects on a Daily Record Questionnaire. Results: ETEC challenge induced a significant increase in fecal ETEC excretion in both groups. However, a statistically significant increase in fecal output was only observed in the probiotic group. ETEC challenge resulted in a decrease in the percentage of fecal dry weight, and an increase in reported Bristol Stool Score, stool frequency and GI complaints. Dietary probiotics significantly decreased the percentage of fecal dry weight. In addition, ETEC increased C-reactive protein, total secretory Immunoglobulin A (IgA) and Immunoglobulin G Colonization Factor Antigen II. Conclusion: Dietary probiotics did not increase resistance to oral attenuated ETEC challenge in human subjects.
Several probiotic strains have been shown to enhance human resistance to infectious disease. It is speculated that these strains may impose this effect by excretion of anti-microbial components, by competing with pathogens for intestinal nutrients and/or mucosal adhesion sites or modulating the immune system.BACKGROUNDSeveral probiotic strains have been shown to enhance human resistance to infectious disease. It is speculated that these strains may impose this effect by excretion of anti-microbial components, by competing with pathogens for intestinal nutrients and/or mucosal adhesion sites or modulating the immune system.A parallel, double-blind, placebo-controlled 4-week intervention was performed in healthy males, to study the effect of a blend of probiotic bacteria (Lactobacillus helveticus Rosell-52, Lactobacillus rhamnosus Rosell-11, Bifidobacterium longum ssp. longum Rosell-175) and a probiotic yeast (Saccharomyces cerevisiae var boulardii CNCM I-1079) on enterotoxigenic Escherichia coli (ETEC) challenge. Primary outcomes studied were fecal ETEC excretion and total fecal output per day.OBJECTIVEA parallel, double-blind, placebo-controlled 4-week intervention was performed in healthy males, to study the effect of a blend of probiotic bacteria (Lactobacillus helveticus Rosell-52, Lactobacillus rhamnosus Rosell-11, Bifidobacterium longum ssp. longum Rosell-175) and a probiotic yeast (Saccharomyces cerevisiae var boulardii CNCM I-1079) on enterotoxigenic Escherichia coli (ETEC) challenge. Primary outcomes studied were fecal ETEC excretion and total fecal output per day.Subjects were randomized to the probiotic (5 × 10(9) colony-forming units (CFUs); twice daily; n=30) or placebo group (twice daily; n=30). After 2 weeks, subjects were orally challenged with a live attenuated ETEC (3 × 10(9) CFU), previously demonstrated to induce mild, short-lived symptoms of a foodborne infection. Before and after ETEC challenge, subjects collected 24 h fecal samples. Compliance to study guidelines, stool consistency (Bristol Stool Score), stool frequency, and frequency and severity of gastrointestinal (GI) complaints were recorded by the subjects on a Daily Record Questionnaire.SUBJECTS/METHODSSubjects were randomized to the probiotic (5 × 10(9) colony-forming units (CFUs); twice daily; n=30) or placebo group (twice daily; n=30). After 2 weeks, subjects were orally challenged with a live attenuated ETEC (3 × 10(9) CFU), previously demonstrated to induce mild, short-lived symptoms of a foodborne infection. Before and after ETEC challenge, subjects collected 24 h fecal samples. Compliance to study guidelines, stool consistency (Bristol Stool Score), stool frequency, and frequency and severity of gastrointestinal (GI) complaints were recorded by the subjects on a Daily Record Questionnaire.ETEC challenge induced a significant increase in fecal ETEC excretion in both groups. However, a statistically significant increase in fecal output was only observed in the probiotic group. ETEC challenge resulted in a decrease in the percentage of fecal dry weight, and an increase in reported Bristol Stool Score, stool frequency and GI complaints. Dietary probiotics significantly decreased the percentage of fecal dry weight. In addition, ETEC increased C-reactive protein, total secretory Immunoglobulin A (IgA) and Immunoglobulin G Colonization Factor Antigen II.RESULTSETEC challenge induced a significant increase in fecal ETEC excretion in both groups. However, a statistically significant increase in fecal output was only observed in the probiotic group. ETEC challenge resulted in a decrease in the percentage of fecal dry weight, and an increase in reported Bristol Stool Score, stool frequency and GI complaints. Dietary probiotics significantly decreased the percentage of fecal dry weight. In addition, ETEC increased C-reactive protein, total secretory Immunoglobulin A (IgA) and Immunoglobulin G Colonization Factor Antigen II.Dietary probiotics did not increase resistance to oral attenuated ETEC challenge in human subjects.CONCLUSIONDietary probiotics did not increase resistance to oral attenuated ETEC challenge in human subjects.
Background: Several probiotic strains have been shown to enhance human resistance to infectious disease. It is speculated that these strains may impose this effect by excretion of anti-microbial components, by competing with pathogens for intestinal nutrients and/or mucosal adhesion sites or modulating the immune system. Objective: A parallel, double-blind, placebo-controlled 4-week intervention was performed in healthy males, to study the effect of a blend of probiotic bacteria (Lactobacillus helveticus Rosell-52, Lactobacillus rhamnosus Rosell-11, Bifidobacterium longum ssp. longum Rosell-175) and a probiotic yeast (Saccharomyces cerevisiae var boulardii CNCM I-1079) on enterotoxigenic Escherichia coli (ETEC) challenge. Primary outcomes studied were fecal ETEC excretion and total fecal output per day.Subjects/ Methods: Subjects were randomized to the probiotic (5 10 super(9) colony-forming units (CFUs); twice daily; n=30) or placebo group (twice daily; n=30). After 2 weeks, subjects were orally challenged with a live attenuated ETEC (3 10 super(9) CFU), previously demonstrated to induce mild, short-lived symptoms of a foodborne infection. Before and after ETEC challenge, subjects collected 24 h fecal samples. Compliance to study guidelines, stool consistency (Bristol Stool Score), stool frequency, and frequency and severity of gastrointestinal (GI) complaints were recorded by the subjects on a Daily Record Questionnaire. Results: ETEC challenge induced a significant increase in fecal ETEC excretion in both groups. However, a statistically significant increase in fecal output was only observed in the probiotic group. ETEC challenge resulted in a decrease in the percentage of fecal dry weight, and an increase in reported Bristol Stool Score, stool frequency and GI complaints. Dietary probiotics significantly decreased the percentage of fecal dry weight. In addition, ETEC increased C-reactive protein, total secretory Immunoglobulin A (IgA) and Immunoglobulin G Colonization Factor Antigen II. Conclusion: Dietary probiotics did not increase resistance to oral attenuated ETEC challenge in human subjects.
Audience Professional
Academic
Author Girard, S A
Tompkins, T A
Floris-Vollenbroek, E G M
Bhardwaj, R
Ten Bruggencate, S J M
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Cites_doi 10.1136/gut.32.1.73
10.1155/2011/312956
10.1542/peds.2011-1379
10.1016/S1043-4526(08)00601-3
10.1016/j.tmaid.2005.10.003
10.1016/j.vaccine.2011.05.021
10.1111/j.1365-2036.2006.03202.x
10.1016/S0016-5085(03)00884-9
10.1053/j.gastro.2005.01.050
10.1016/j.ijmm.2012.11.006
10.1086/338640
10.1128/CMR.00022-13
10.1093/jn/136.1.70
10.1111/j.1651-2227.2007.00191.x
10.1016/S1473-3099(06)70495-9
10.1080/08035250410022521
10.1023/A:1018924820333
10.3748/wjg.v16.i18.2202
10.1093/oxfordjournals.aje.a116788
10.1016/j.idc.2012.06.002
10.1136/bmj.39255.829120.47
10.1016/j.vaccine.2011.06.084
10.4269/ajtmh.2008.78.214
10.1186/1471-2334-10-330
10.1007/s10620-009-0822-4
10.1128/IAI.67.1.302-307.1999
10.1017/S0007114513002547
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References McFarland (CR2) 2007; 335
McFarland (CR7) 2010; 16
Corr, Hill, Gahan (CR25) 2009; 56
Kollaritsch, Paulke-Korinek, Wiedermann (CR21) 2012; 26
Levine, Ferreccio, Prado, Cayazzo, Abrego, Martinez (CR17) 1993; 138
McFarland (CR5) 2007; 5
Isidean, Riddle, Savarino, Porter (CR18) 2011; 29
Croxen, Law, Scholz, Keeney, Wlodarska, Finlay (CR23) 2013; 26
Htwe, Yee, Tin, Vandenplas (CR9) 2008; 78
Szajewska, Skorka, Dylag (CR8) 2007; 25
Rund, Rohde, Sonnenborn, Oelschlaeger (CR28) 2013; 303
Kollaritsch, Holst, Grobara, Wiedermann (CR12) 1993; 111
Ten Bruggencate, Bovee-Oudenhoven, Lettink-Wissink, Katan, van der Meer (CR15) 2006; 136
Bisson, Hidalgo, Rozan, Messaoudi (CR13) 2010; 55
Sazawal, Hiremath, Dhingra, Malik, Deb, Black (CR6) 2006; 6
Agustina, Kok, van de Rest, Fahmida, Firmansyah, Lukito (CR4) 2012; 129
CR24
Klein, Elmer, McFarland, Surawicz, Levy (CR16) 1993; 10
Villarruel, Rubio, Lopez, Cintioni, Gurevech, Romero (CR11) 2007; 96
Castagliuolo, Riegler, Valenick, LaMont, Pothoulakis (CR26) 1999; 67
Paton, Jennings, Morona, Wang, Focareta, Roddam (CR27) 2005; 128
Schjorring, Krogfelt (CR3) 2011; 2011
Bovee-Oudenhoven, Lettink-Wissink, Van Doesburg, Witteman, Van Der Meer (CR14) 2003; 125
Rendi-Wagner, Kollaritsch (CR22) 2002; 34
Heaton, Ghosh, Braddon (CR19) 1991; 32
Porter, Riddle, Tribble, Louis Bougeois, McKenzie, Isidean (CR20) 2011; 29
Field, Gautret, Schlagenhauf, Burchard, Caumes, Jensenius (CR1) 2010; 10
Kurugol, Koturoglu (CR10) 2005; 94
MM Levine (BFejcn2014238_CR17) 1993; 138
LV McFarland (BFejcn2014238_CR2) 2007; 335
P Rendi-Wagner (BFejcn2014238_CR22) 2002; 34
CK Porter (BFejcn2014238_CR20) 2011; 29
K Htwe (BFejcn2014238_CR9) 2008; 78
SJ Ten Bruggencate (BFejcn2014238_CR15) 2006; 136
I Castagliuolo (BFejcn2014238_CR26) 1999; 67
G Villarruel (BFejcn2014238_CR11) 2007; 96
H Kollaritsch (BFejcn2014238_CR21) 2012; 26
AW Paton (BFejcn2014238_CR27) 2005; 128
IM Bovee-Oudenhoven (BFejcn2014238_CR14) 2003; 125
R Agustina (BFejcn2014238_CR4) 2012; 129
H Szajewska (BFejcn2014238_CR8) 2007; 25
BFejcn2014238_CR24
MA Croxen (BFejcn2014238_CR23) 2013; 26
H Kollaritsch (BFejcn2014238_CR12) 1993; 111
S Sazawal (BFejcn2014238_CR6) 2006; 6
SA Rund (BFejcn2014238_CR28) 2013; 303
LV McFarland (BFejcn2014238_CR5) 2007; 5
SM Klein (BFejcn2014238_CR16) 1993; 10
V Field (BFejcn2014238_CR1) 2010; 10
LV McFarland (BFejcn2014238_CR7) 2010; 16
Z Kurugol (BFejcn2014238_CR10) 2005; 94
JF Bisson (BFejcn2014238_CR13) 2010; 55
SD Isidean (BFejcn2014238_CR18) 2011; 29
KW Heaton (BFejcn2014238_CR19) 1991; 32
SC Corr (BFejcn2014238_CR25) 2009; 56
S Schjorring (BFejcn2014238_CR3) 2011; 2011
16728323 - Lancet Infect Dis. 2006 Jun;6(6):374-82
21083874 - BMC Infect Dis. 2010 Nov 17;10:330
8290474 - Pharm Res. 1993 Nov;10(11):1615-9
20458757 - World J Gastroenterol. 2010 May 14;16(18):2202-22
1991641 - Gut. 1991 Jan;32(1):73-9
23312798 - Int J Med Microbiol. 2013 Jan;303(1):1-8
22492764 - Pediatrics. 2012 May;129(5):e1155-64
17269987 - Aliment Pharmacol Ther. 2007 Feb 1;25(3):257-64
24092857 - Clin Microbiol Rev. 2013 Oct;26(4):822-80
19437118 - Dig Dis Sci. 2010 Apr;55(4):911-9
18256417 - Am J Trop Med Hyg. 2008 Feb;78(2):214-6
17298915 - Travel Med Infect Dis. 2007 Mar;5(2):97-105
15858959 - Acta Paediatr. 2005 Jan;94(1):44-7
23930950 - Br J Nutr. 2014 Feb;111(3):465-73
15887106 - Gastroenterology. 2005 May;128(5):1219-28
9864230 - Infect Immun. 1999 Jan;67(1):302-7
17626915 - BMJ. 2007 Jul 14;335(7610):54-5
16365061 - J Nutr. 2006 Jan;136(1):70-4
11803509 - Clin Infect Dis. 2002 Mar 1;34(5):628-33
21616116 - Vaccine. 2011 Aug 11;29(35):5869-85
21318188 - Int J Microbiol. 2011;2011:312956
8486328 - Fortschr Med. 1993 Mar 30;111(9):152-6
19389605 - Adv Food Nutr Res. 2009;56:1-15
17306006 - Acta Paediatr. 2007 Apr;96(4):538-41
8237973 - Am J Epidemiol. 1993 Nov 15;138(10):849-69
21723899 - Vaccine. 2011 Aug 26;29(37):6167-78
12891550 - Gastroenterology. 2003 Aug;125(2):469-76
22963778 - Infect Dis Clin North Am. 2012 Sep;26(3):691-706
References_xml – volume: 32
  start-page: 73
  year: 1991
  end-page: 79
  ident: CR19
  article-title: How bad are the symptoms and bowel dysfunction of patients with the irritable bowel syndrome? A prospective, controlled study with emphasis on stool form
  publication-title: Gut
  doi: 10.1136/gut.32.1.73
– volume: 2011
  start-page: 312956
  year: 2011
  ident: CR3
  article-title: Assessment of bacterial antibiotic resistance transfer in the gut
  publication-title: Int J Microbiol
  doi: 10.1155/2011/312956
– volume: 129
  start-page: e1155
  year: 2012
  end-page: e1164
  ident: CR4
  article-title: Randomized trial of probiotics and calcium on diarrhea and respiratory tract infections in Indonesian children
  publication-title: Pediatrics
  doi: 10.1542/peds.2011-1379
– volume: 56
  start-page: 1
  year: 2009
  end-page: 15
  ident: CR25
  article-title: Understanding the mechanisms by which probiotics inhibit gastrointestinal pathogens
  publication-title: Adv Food Nutr Res
  doi: 10.1016/S1043-4526(08)00601-3
– volume: 5
  start-page: 97
  year: 2007
  end-page: 105
  ident: CR5
  article-title: Meta-analysis of probiotics for the prevention of traveler's diarrhea
  publication-title: Travel Med Infect Dis
  doi: 10.1016/j.tmaid.2005.10.003
– volume: 29
  start-page: 5869
  year: 2011
  end-page: 5885
  ident: CR20
  article-title: A systematic review of experimental infections with enterotoxigenic (ETEC)
  publication-title: Vaccine
  doi: 10.1016/j.vaccine.2011.05.021
– volume: 25
  start-page: 257
  year: 2007
  end-page: 264
  ident: CR8
  article-title: Meta-analysis: for treating acute diarrhoea in children
  publication-title: Aliment Pharmacol Ther
  doi: 10.1111/j.1365-2036.2006.03202.x
– volume: 125
  start-page: 469
  year: 2003
  end-page: 476
  ident: CR14
  article-title: Diarrhea caused by enterotoxigenic infection of humans is inhibited by dietary calcium
  publication-title: Gastroenterology
  doi: 10.1016/S0016-5085(03)00884-9
– volume: 128
  start-page: 1219
  year: 2005
  end-page: 1228
  ident: CR27
  article-title: Recombinant probiotics for treatment and prevention of enterotoxigenic diarrhea
  publication-title: Gastroenterology
  doi: 10.1053/j.gastro.2005.01.050
– volume: 303
  start-page: 1
  year: 2013
  end-page: 8
  ident: CR28
  article-title: Antagonistic effects of probiotic Nissle 1917 on EHEC strains of serotype O104:H4 and O157:H7
  publication-title: Int J Med Microbiol
  doi: 10.1016/j.ijmm.2012.11.006
– volume: 34
  start-page: 628
  year: 2002
  end-page: 633
  ident: CR22
  article-title: Drug prophylaxis for travelers' diarrhea
  publication-title: Clin Infect Dis
  doi: 10.1086/338640
– volume: 67
  start-page: 302
  year: 1999
  end-page: 307
  ident: CR26
  article-title: protease inhibits the effects of toxins A and B in human colonic mucosa
  publication-title: Infect Immun
– volume: 26
  start-page: 822
  year: 2013
  end-page: 880
  ident: CR23
  article-title: Recent Advances in Understanding Enteric Pathogenic Escherichia coli
  publication-title: Clin Microbiol Rev
  doi: 10.1128/CMR.00022-13
– volume: 111
  start-page: 152
  year: 1993
  end-page: 156
  ident: CR12
  article-title: [Prevention of traveler's diarrhea with Saccharomyces boulardii. Results of a placebo controlled double-blind study]
  publication-title: Fortschr Med
– volume: 136
  start-page: 70
  year: 2006
  end-page: 74
  ident: CR15
  article-title: Dietary fructooligosaccharides affect intestinal barrier function in healthy men
  publication-title: J Nutr
  doi: 10.1093/jn/136.1.70
– volume: 96
  start-page: 538
  year: 2007
  end-page: 541
  ident: CR11
  article-title: in acute childhood diarrhoea: a randomized, placebo-controlled study
  publication-title: Acta Paediatr
  doi: 10.1111/j.1651-2227.2007.00191.x
– volume: 6
  start-page: 374
  year: 2006
  end-page: 382
  ident: CR6
  article-title: Efficacy of probiotics in prevention of acute diarrhoea: a meta-analysis of masked, randomised, placebo-controlled trials
  publication-title: Lancet Infect Dis
  doi: 10.1016/S1473-3099(06)70495-9
– volume: 94
  start-page: 44
  year: 2005
  end-page: 47
  ident: CR10
  article-title: Effects of Saccharomyces boulardii in children with acute diarrhoea
  publication-title: Acta Paediatr
  doi: 10.1080/08035250410022521
– volume: 10
  start-page: 1615
  year: 1993
  end-page: 1619
  ident: CR16
  article-title: Recovery and elimination of the biotherapeutic agent, Saccharomyces boulardii, in healthy human volunteers
  publication-title: Pharm Res
  doi: 10.1023/A:1018924820333
– volume: 16
  start-page: 2202
  year: 2010
  end-page: 2222
  ident: CR7
  article-title: Systematic review and meta-analysis of Saccharomyces boulardii in adult patients
  publication-title: World J Gastroenterol
  doi: 10.3748/wjg.v16.i18.2202
– volume: 138
  start-page: 849
  year: 1993
  end-page: 869
  ident: CR17
  article-title: Epidemiologic studies of diarrheal infections in a low socioeconomic level peri-urban community in Santiago, Chile
  publication-title: Am J Epidemiol
  doi: 10.1093/oxfordjournals.aje.a116788
– volume: 26
  start-page: 691
  year: 2012
  end-page: 706
  ident: CR21
  article-title: Traveler's Diarrhea
  publication-title: Infect Dis Clin North Am
  doi: 10.1016/j.idc.2012.06.002
– volume: 335
  start-page: 54
  year: 2007
  end-page: 55
  ident: CR2
  article-title: Diarrhoea associated with antibiotic use
  publication-title: BMJ
  doi: 10.1136/bmj.39255.829120.47
– volume: 29
  start-page: 6167
  year: 2011
  end-page: 6178
  ident: CR18
  article-title: A systematic review of ETEC epidemiology focusing on colonization factor and toxin expression
  publication-title: Vaccine
  doi: 10.1016/j.vaccine.2011.06.084
– volume: 78
  start-page: 214
  year: 2008
  end-page: 216
  ident: CR9
  article-title: Effect of in the treatment of acute watery diarrhea in Myanmar children: a randomized controlled study
  publication-title: Am J Trop Med Hyg
  doi: 10.4269/ajtmh.2008.78.214
– volume: 10
  start-page: 330
  year: 2010
  ident: CR1
  article-title: Travel and migration associated infectious diseases morbidity in Europe, 2008
  publication-title: BMC Infect Dis
  doi: 10.1186/1471-2334-10-330
– ident: CR24
– volume: 55
  start-page: 911
  year: 2010
  end-page: 919
  ident: CR13
  article-title: Preventive effects of different probiotic formulations on travelers' diarrhea model in wistar rats: preventive effects of probiotics on TD
  publication-title: Dig Dis Sci
  doi: 10.1007/s10620-009-0822-4
– volume: 10
  start-page: 330
  year: 2010
  ident: BFejcn2014238_CR1
  publication-title: BMC Infect Dis
  doi: 10.1186/1471-2334-10-330
– volume: 16
  start-page: 2202
  year: 2010
  ident: BFejcn2014238_CR7
  publication-title: World J Gastroenterol
  doi: 10.3748/wjg.v16.i18.2202
– volume: 26
  start-page: 822
  year: 2013
  ident: BFejcn2014238_CR23
  publication-title: Clin Microbiol Rev
  doi: 10.1128/CMR.00022-13
– volume: 29
  start-page: 5869
  year: 2011
  ident: BFejcn2014238_CR20
  publication-title: Vaccine
  doi: 10.1016/j.vaccine.2011.05.021
– volume: 10
  start-page: 1615
  year: 1993
  ident: BFejcn2014238_CR16
  publication-title: Pharm Res
  doi: 10.1023/A:1018924820333
– volume: 138
  start-page: 849
  year: 1993
  ident: BFejcn2014238_CR17
  publication-title: Am J Epidemiol
  doi: 10.1093/oxfordjournals.aje.a116788
– volume: 5
  start-page: 97
  year: 2007
  ident: BFejcn2014238_CR5
  publication-title: Travel Med Infect Dis
  doi: 10.1016/j.tmaid.2005.10.003
– volume: 34
  start-page: 628
  year: 2002
  ident: BFejcn2014238_CR22
  publication-title: Clin Infect Dis
  doi: 10.1086/338640
– volume: 56
  start-page: 1
  year: 2009
  ident: BFejcn2014238_CR25
  publication-title: Adv Food Nutr Res
  doi: 10.1016/S1043-4526(08)00601-3
– volume: 303
  start-page: 1
  year: 2013
  ident: BFejcn2014238_CR28
  publication-title: Int J Med Microbiol
  doi: 10.1016/j.ijmm.2012.11.006
– volume: 335
  start-page: 54
  year: 2007
  ident: BFejcn2014238_CR2
  publication-title: BMJ
  doi: 10.1136/bmj.39255.829120.47
– volume: 67
  start-page: 302
  year: 1999
  ident: BFejcn2014238_CR26
  publication-title: Infect Immun
  doi: 10.1128/IAI.67.1.302-307.1999
– volume: 111
  start-page: 152
  year: 1993
  ident: BFejcn2014238_CR12
  publication-title: Fortschr Med
– volume: 55
  start-page: 911
  year: 2010
  ident: BFejcn2014238_CR13
  publication-title: Dig Dis Sci
  doi: 10.1007/s10620-009-0822-4
– volume: 25
  start-page: 257
  year: 2007
  ident: BFejcn2014238_CR8
  publication-title: Aliment Pharmacol Ther
  doi: 10.1111/j.1365-2036.2006.03202.x
– volume: 26
  start-page: 691
  year: 2012
  ident: BFejcn2014238_CR21
  publication-title: Infect Dis Clin North Am
  doi: 10.1016/j.idc.2012.06.002
– volume: 129
  start-page: e1155
  year: 2012
  ident: BFejcn2014238_CR4
  publication-title: Pediatrics
  doi: 10.1542/peds.2011-1379
– ident: BFejcn2014238_CR24
  doi: 10.1017/S0007114513002547
– volume: 125
  start-page: 469
  year: 2003
  ident: BFejcn2014238_CR14
  publication-title: Gastroenterology
  doi: 10.1016/S0016-5085(03)00884-9
– volume: 32
  start-page: 73
  year: 1991
  ident: BFejcn2014238_CR19
  publication-title: Gut
  doi: 10.1136/gut.32.1.73
– volume: 2011
  start-page: 312956
  year: 2011
  ident: BFejcn2014238_CR3
  publication-title: Int J Microbiol
  doi: 10.1155/2011/312956
– volume: 6
  start-page: 374
  year: 2006
  ident: BFejcn2014238_CR6
  publication-title: Lancet Infect Dis
  doi: 10.1016/S1473-3099(06)70495-9
– volume: 29
  start-page: 6167
  year: 2011
  ident: BFejcn2014238_CR18
  publication-title: Vaccine
  doi: 10.1016/j.vaccine.2011.06.084
– volume: 96
  start-page: 538
  year: 2007
  ident: BFejcn2014238_CR11
  publication-title: Acta Paediatr
  doi: 10.1111/j.1651-2227.2007.00191.x
– volume: 78
  start-page: 214
  year: 2008
  ident: BFejcn2014238_CR9
  publication-title: Am J Trop Med Hyg
  doi: 10.4269/ajtmh.2008.78.214
– volume: 136
  start-page: 70
  year: 2006
  ident: BFejcn2014238_CR15
  publication-title: J Nutr
  doi: 10.1093/jn/136.1.70
– volume: 128
  start-page: 1219
  year: 2005
  ident: BFejcn2014238_CR27
  publication-title: Gastroenterology
  doi: 10.1053/j.gastro.2005.01.050
– volume: 94
  start-page: 44
  year: 2005
  ident: BFejcn2014238_CR10
  publication-title: Acta Paediatr
  doi: 10.1080/08035250410022521
– reference: 21083874 - BMC Infect Dis. 2010 Nov 17;10:330
– reference: 23312798 - Int J Med Microbiol. 2013 Jan;303(1):1-8
– reference: 23930950 - Br J Nutr. 2014 Feb;111(3):465-73
– reference: 16728323 - Lancet Infect Dis. 2006 Jun;6(6):374-82
– reference: 17298915 - Travel Med Infect Dis. 2007 Mar;5(2):97-105
– reference: 19389605 - Adv Food Nutr Res. 2009;56:1-15
– reference: 22492764 - Pediatrics. 2012 May;129(5):e1155-64
– reference: 15858959 - Acta Paediatr. 2005 Jan;94(1):44-7
– reference: 21616116 - Vaccine. 2011 Aug 11;29(35):5869-85
– reference: 1991641 - Gut. 1991 Jan;32(1):73-9
– reference: 20458757 - World J Gastroenterol. 2010 May 14;16(18):2202-22
– reference: 24092857 - Clin Microbiol Rev. 2013 Oct;26(4):822-80
– reference: 21318188 - Int J Microbiol. 2011;2011:312956
– reference: 17269987 - Aliment Pharmacol Ther. 2007 Feb 1;25(3):257-64
– reference: 8486328 - Fortschr Med. 1993 Mar 30;111(9):152-6
– reference: 12891550 - Gastroenterology. 2003 Aug;125(2):469-76
– reference: 8237973 - Am J Epidemiol. 1993 Nov 15;138(10):849-69
– reference: 15887106 - Gastroenterology. 2005 May;128(5):1219-28
– reference: 17626915 - BMJ. 2007 Jul 14;335(7610):54-5
– reference: 9864230 - Infect Immun. 1999 Jan;67(1):302-7
– reference: 19437118 - Dig Dis Sci. 2010 Apr;55(4):911-9
– reference: 16365061 - J Nutr. 2006 Jan;136(1):70-4
– reference: 21723899 - Vaccine. 2011 Aug 26;29(37):6167-78
– reference: 11803509 - Clin Infect Dis. 2002 Mar 1;34(5):628-33
– reference: 22963778 - Infect Dis Clin North Am. 2012 Sep;26(3):691-706
– reference: 17306006 - Acta Paediatr. 2007 Apr;96(4):538-41
– reference: 8290474 - Pharm Res. 1993 Nov;10(11):1615-9
– reference: 18256417 - Am J Trop Med Hyg. 2008 Feb;78(2):214-6
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Snippet Background: Several probiotic strains have been shown to enhance human resistance to infectious disease. It is speculated that these strains may impose this...
Several probiotic strains have been shown to enhance human resistance to infectious disease. It is speculated that these strains may impose this effect by...
BACKGROUND: Several probiotic strains have been shown to enhance human resistance to infectious disease. It is speculated that these strains may impose this...
SUBJECTS/METHODS: Subjects were randomized to the probiotic (5 x [10.sup.9] colony-forming units (CFUs);twice daily;n = 30) or placebo group (twice daily; n =...
Background:Several probiotic strains have been shown to enhance human resistance to infectious disease. It is speculated that these strains may impose this...
Background: Several probiotic strains have been shown to enhance human resistance to infectious disease. It is speculated that these strains may impose this...
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StartPage 385
SubjectTerms 692/1807/1808
692/699/1503/1501
Adhesion
Adult
Antigens
Bifidobacterium
Bifidobacterium longum
C-reactive protein
Clinical Nutrition
Colonization
Colonization factor
Defecation
Diarrhea - microbiology
Diarrhea - prevention & control
Disease resistance
Double-Blind Method
Double-blind studies
E coli
Epidemiology
Escherichia coli
Escherichia coli Infections - microbiology
Escherichia coli Infections - prevention & control
Excretion
Feces
Feces - microbiology
Foodborne diseases
Humans
IgG antibody
Immune system
Immunocompetent cells
Immunoglobulin A
Immunoglobulin G
Immunoglobulins
Infectious diseases
Internal Medicine
Intestine
Intestines - microbiology
Lactobacilli
Lactobacillus
Lactobacillus acidophilus
Lactobacillus helveticus
Lactobacillus rhamnosus
Male
Medicine
Medicine & Public Health
Metabolic Diseases
Microorganisms
Mucosa
Nutrients
original-article
Pathogens
Physiological aspects
Preventive medicine
Probiotics
Probiotics - therapeutic use
Public Health
Randomization
Saccharomyces cerevisiae
Signs and symptoms
Statistical analysis
Statistical methods
Strains (organisms)
Weight
Yeast
Yeasts
Yogurt
Young Adult
Title The effect of a multi-strain probiotic on the resistance toward Escherichia coli challenge in a randomized, placebo-controlled, double-blind intervention study
URI https://link.springer.com/article/10.1038/ejcn.2014.238
https://www.ncbi.nlm.nih.gov/pubmed/25369827
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