Skip to main content
Top
Published in: BMC Pediatrics 1/2017

Open Access 01-12-2017 | Research article

Safety and tolerability of Bifidobacterium longum subspecies infantis EVC001 supplementation in healthy term breastfed infants: a phase I clinical trial

Authors: Jennifer T. Smilowitz, Jackelyn Moya, Melissa A. Breck, Chelsea Cook, Annette Fineberg, Kathleen Angkustsiri, Mark A. Underwood

Published in: BMC Pediatrics | Issue 1/2017

Login to get access

Abstract

Background

Historically, bifidobacteria were the dominant intestinal bacteria in breastfed infants. Still abundant in infants in developing nations, levels of intestinal bifidobacteria are low among infants in developed nations. Recent studies have described an intimate relationship between human milk and a specific subspecies of Bifidobacterium, B. longum subsp. infantis (B. infantis), yet supplementation of breastfed, healthy, term infants with this organism, has not been reported. The IMPRINT Study, a Phase I clinical trial, was initiated to determine the safety and tolerability of supplementing breastfed infants with B. infantis (EVC001).

Methods

Eighty mother-infant dyads were enrolled in either lactation support plus B. infantis supplementation (BiLS) or lactation support alone (LS). Starting with Day 7 postnatal, BiLS infants were fed 1.8–2.8 × 1010 CFU B. infantis EVC001 daily in breast milk for 21 days. Mothers collected fecal samples, filled out health questionnaires, and kept daily logs about their infants’ feeding and gastrointestinal symptoms from birth until Day 61 postnatal. Safety and tolerability were determined from maternal reports.

Results

There were no differences in the mean gestational age at birth, weight 1 and 2 months postnatal, and breast milk intake between groups. The mean Log10 change in fecal Bifidobacterium from Day 6 to Day 28 was higher (p = 0.0002) for BiLS (6.6 ± 2.8 SD) than for LS infants (3.5 ± 3.5 SD). Daily stool number was higher (p < 0.005) for LS and lower (p < 0.05) for BiLS infants during supplementation than at Baseline. During supplementation, watery stools decreased and soft stools increased by 36% over baseline in BiLS infants (p < 0.05) with no significant changes in stool consistency for the LS infants. None of the safety and tolerability endpoints, including flatulence, bloody stool, body temperature, ratings of gastrointestinal symptoms, use of antibiotics or gas-relieving medications, infant colic, jaundice, number of illnesses, sick doctor visits, or diagnoses of eczema were different for the groups at any point.

Conclusions

The B. infantis EVC001 supplement was safely consumed and well-tolerated. Stools were fewer and better formed in infants in the BiLS group compared with LS group. Adverse events were those expected in healthy infants and not different between groups.

Trial registration

ClinicalTrials.gov NCT02457338. Registered May 27, 2015.
Appendix
Available only for authorised users
Literature
1.
go back to reference Smilowitz JT, Lebrilla CB, Mills DA, German JB, Freeman SL. Breast milk oligosaccharides: structure-function relationships in the neonate. Annu Rev Nutr. 2014;34:143–69.CrossRefPubMedPubMedCentral Smilowitz JT, Lebrilla CB, Mills DA, German JB, Freeman SL. Breast milk oligosaccharides: structure-function relationships in the neonate. Annu Rev Nutr. 2014;34:143–69.CrossRefPubMedPubMedCentral
2.
go back to reference Coppa GV, Gabrielli O, Pierani P, Catassi C, Carlucci A, Giorgi P. Changes in carbohydrate composition in human milk over 4 months of lactation. Pediatrics. 1993;91(5):637–41.PubMed Coppa GV, Gabrielli O, Pierani P, Catassi C, Carlucci A, Giorgi P. Changes in carbohydrate composition in human milk over 4 months of lactation. Pediatrics. 1993;91(5):637–41.PubMed
3.
go back to reference Chaturvedi P, Warren CD, Altaye M, Morrow AL, Ruiz-Palacios G, Pickering LK, et al. Fucosylated human milk oligosaccharides vary between individuals and over the course of lactation. Glycobiology. 2001;11(5):365–72.CrossRefPubMed Chaturvedi P, Warren CD, Altaye M, Morrow AL, Ruiz-Palacios G, Pickering LK, et al. Fucosylated human milk oligosaccharides vary between individuals and over the course of lactation. Glycobiology. 2001;11(5):365–72.CrossRefPubMed
4.
go back to reference Zivkovic AM, German JB, Lebrilla CB, Mills DA. Human milk glycobiome and its impact on the infant gastrointestinal microbiota. Proc Natl Acad Sci U S A. 2011;108(Suppl 1):4653–8.CrossRefPubMed Zivkovic AM, German JB, Lebrilla CB, Mills DA. Human milk glycobiome and its impact on the infant gastrointestinal microbiota. Proc Natl Acad Sci U S A. 2011;108(Suppl 1):4653–8.CrossRefPubMed
5.
go back to reference Tissier H. Recherches sur la flore intestinale des nourrissons: état normal et pathologique. Paris: G. Carré et C. Naud; 1900. Tissier H. Recherches sur la flore intestinale des nourrissons: état normal et pathologique. Paris: G. Carré et C. Naud; 1900.
6.
go back to reference Subramanian S, Blanton LV, Frese SA, Charbonneau M, Mills DA, Gordon JI. Cultivating healthy growth and nutrition through the gut microbiota. Cell. 2015;161(1):36–48.CrossRefPubMedPubMedCentral Subramanian S, Blanton LV, Frese SA, Charbonneau M, Mills DA, Gordon JI. Cultivating healthy growth and nutrition through the gut microbiota. Cell. 2015;161(1):36–48.CrossRefPubMedPubMedCentral
7.
go back to reference Bäckhed F, Roswall J, Peng Y, Feng Q, Jia H, Kovatcheva-Datchary P, et al. Dynamics and stabilization of the human gut Microbiome during the first year of life. Cell Host Microbe. 2015;17(5):690–703.CrossRefPubMed Bäckhed F, Roswall J, Peng Y, Feng Q, Jia H, Kovatcheva-Datchary P, et al. Dynamics and stabilization of the human gut Microbiome during the first year of life. Cell Host Microbe. 2015;17(5):690–703.CrossRefPubMed
8.
go back to reference Sela D, Chapman J, Adeuya A, Kim J, Chen F, Whitehead T, et al. The genome sequence of Bifidobacterium longum subsp. infantis reveals adaptations for milk utilization within the infant microbiome. Proc Natl Acad Sci. 2008;105(48):18964.CrossRefPubMedPubMedCentral Sela D, Chapman J, Adeuya A, Kim J, Chen F, Whitehead T, et al. The genome sequence of Bifidobacterium longum subsp. infantis reveals adaptations for milk utilization within the infant microbiome. Proc Natl Acad Sci. 2008;105(48):18964.CrossRefPubMedPubMedCentral
9.
go back to reference LoCascio R, Ninonuevo M, Freeman S, Sela D, Grimm R, Lebrilla C, et al. Glycoprofiling of bifidobacterial consumption of human milk oligosaccharides demonstrates strain specific, preferential consumption of small chain glycans secreted in early human lactation. J Agric Food Chem. 2007;55(22):8914–9.CrossRefPubMed LoCascio R, Ninonuevo M, Freeman S, Sela D, Grimm R, Lebrilla C, et al. Glycoprofiling of bifidobacterial consumption of human milk oligosaccharides demonstrates strain specific, preferential consumption of small chain glycans secreted in early human lactation. J Agric Food Chem. 2007;55(22):8914–9.CrossRefPubMed
10.
go back to reference Garrido D, Ruiz-Moyano S, Lemay DG, Sela DA, German JB, Mills DA: Comparative transcriptomics reveals key differences in the response to milk oligosaccharides of infant gut-associated bifidobacteria. Scientific reports. 2015;5:1-7. Garrido D, Ruiz-Moyano S, Lemay DG, Sela DA, German JB, Mills DA: Comparative transcriptomics reveals key differences in the response to milk oligosaccharides of infant gut-associated bifidobacteria. Scientific reports. 2015;5:1-7.
11.
go back to reference Garrido D, Barile D, Mills DA. A molecular basis for bifidobacterial enrichment in the infant gastrointestinal tract. Advances in Nutrition: An International Review Journal. 2012;3(3):415S–21S.CrossRef Garrido D, Barile D, Mills DA. A molecular basis for bifidobacterial enrichment in the infant gastrointestinal tract. Advances in Nutrition: An International Review Journal. 2012;3(3):415S–21S.CrossRef
12.
go back to reference Kim JH, An HJ, Garrido D, German JB, Lebrilla CB, Mills DA. Proteomic analysis of Bifidobacterium longum subsp. infantis reveals the metabolic insight on consumption of prebiotics and host glycans. PLoS One. 2013;8(2):e57535.CrossRefPubMedPubMedCentral Kim JH, An HJ, Garrido D, German JB, Lebrilla CB, Mills DA. Proteomic analysis of Bifidobacterium longum subsp. infantis reveals the metabolic insight on consumption of prebiotics and host glycans. PLoS One. 2013;8(2):e57535.CrossRefPubMedPubMedCentral
13.
go back to reference Garrido D, Ruiz-Moyano S, Mills DA. Release and utilization of N-acetyl-D-glucosamine from human milk oligosaccharides by Bifidobacterium longum subsp. infantis. Anaerobe. 2012;18(4):430–5.CrossRefPubMed Garrido D, Ruiz-Moyano S, Mills DA. Release and utilization of N-acetyl-D-glucosamine from human milk oligosaccharides by Bifidobacterium longum subsp. infantis. Anaerobe. 2012;18(4):430–5.CrossRefPubMed
14.
go back to reference Ward R, Niñonuevo M, Mills D, Lebrilla C, German J. In vitro fermentability of human milk oligosaccharides by several strains of bifidobacteria. Mol Nutr Food Res. 2007;51(11):1398–405.CrossRefPubMed Ward R, Niñonuevo M, Mills D, Lebrilla C, German J. In vitro fermentability of human milk oligosaccharides by several strains of bifidobacteria. Mol Nutr Food Res. 2007;51(11):1398–405.CrossRefPubMed
15.
go back to reference Chichlowski M, De Lartigue G, German JB, Raybould HE, Mills DA. Bifidobacteria isolated from infants and cultured on human milk oligosaccharides affect intestinal epithelial function. J Pediatr Gastroenterol Nutr. 2012;55(3):321–7.CrossRefPubMedPubMedCentral Chichlowski M, De Lartigue G, German JB, Raybould HE, Mills DA. Bifidobacteria isolated from infants and cultured on human milk oligosaccharides affect intestinal epithelial function. J Pediatr Gastroenterol Nutr. 2012;55(3):321–7.CrossRefPubMedPubMedCentral
16.
go back to reference Underwood MA, German JB, Lebrilla CB, Mills DA: Bifidobacterium longum subspecies infantis: champion colonizer of the infant gut. Pediatr Res. 2014;77(1-2):229-35. Underwood MA, German JB, Lebrilla CB, Mills DA: Bifidobacterium longum subspecies infantis: champion colonizer of the infant gut. Pediatr Res. 2014;77(1-2):229-35.
18.
go back to reference Ganguli K, Meng D, Rautava S, Lu L, Walker WA, Nanthakumar N. Probiotics prevent necrotizing enterocolitis by modulating enterocyte genes that regulate innate immune-mediated inflammation. American Journal of Physiology-Gastrointestinal and Liver Physiology. 2013;304(2):G132–41.CrossRefPubMed Ganguli K, Meng D, Rautava S, Lu L, Walker WA, Nanthakumar N. Probiotics prevent necrotizing enterocolitis by modulating enterocyte genes that regulate innate immune-mediated inflammation. American Journal of Physiology-Gastrointestinal and Liver Physiology. 2013;304(2):G132–41.CrossRefPubMed
19.
go back to reference Underwood MA, Arriola J, Gerber CW, Kaveti A, Kalanetra KM, Kananurak A, et al. Bifidobacterium longum subsp. infantis in experimental necrotizing enterocolitis: alterations in inflammation, innate immune response, and the microbiota. Pediatr Res. 2014;76(4):326–33.CrossRefPubMedPubMedCentral Underwood MA, Arriola J, Gerber CW, Kaveti A, Kalanetra KM, Kananurak A, et al. Bifidobacterium longum subsp. infantis in experimental necrotizing enterocolitis: alterations in inflammation, innate immune response, and the microbiota. Pediatr Res. 2014;76(4):326–33.CrossRefPubMedPubMedCentral
20.
go back to reference Bergmann KR, Liu SX, Tian R, Kushnir A, Turner JR, Li H-L, et al. Bifidobacteria stabilize claudins at tight junctions and prevent intestinal barrier dysfunction in mouse necrotizing enterocolitis. Am J Pathol. 2013;182(5):1595–606.CrossRefPubMedPubMedCentral Bergmann KR, Liu SX, Tian R, Kushnir A, Turner JR, Li H-L, et al. Bifidobacteria stabilize claudins at tight junctions and prevent intestinal barrier dysfunction in mouse necrotizing enterocolitis. Am J Pathol. 2013;182(5):1595–606.CrossRefPubMedPubMedCentral
21.
go back to reference Huda M, Lewis Z, Kalanetra K, Rashid M, Raqib R, Qadri F, et al. Stool microbiota and vaccine responses of infants. Pediatrics. 2014;134:1–11.CrossRef Huda M, Lewis Z, Kalanetra K, Rashid M, Raqib R, Qadri F, et al. Stool microbiota and vaccine responses of infants. Pediatrics. 2014;134:1–11.CrossRef
22.
go back to reference Lewis ZT, Totten SM, Smilowitz JT, Popovic M, Parker E, Lemay DG, et al. Maternal fucosyltransferase 2 status affects the gut bifidobacterial communities of breastfed infants. Microbiome. 2015;3(1):13.CrossRefPubMedPubMedCentral Lewis ZT, Totten SM, Smilowitz JT, Popovic M, Parker E, Lemay DG, et al. Maternal fucosyltransferase 2 status affects the gut bifidobacterial communities of breastfed infants. Microbiome. 2015;3(1):13.CrossRefPubMedPubMedCentral
23.
go back to reference Bager P, Wohlfahrt J, Westergaard T. Caesarean delivery and risk of atopy and allergic disesase: meta-analyses. Clinical & Experimental Allergy. 2008;38(4):634–42.CrossRef Bager P, Wohlfahrt J, Westergaard T. Caesarean delivery and risk of atopy and allergic disesase: meta-analyses. Clinical & Experimental Allergy. 2008;38(4):634–42.CrossRef
24.
go back to reference Thavagnanam S, Fleming J, Bromley A, Shields M, Cardwell C. A meta-analysis of the association between Caesarean section and childhood asthma. Clinical & Experimental Allergy. 2008;38(4):629–33.CrossRef Thavagnanam S, Fleming J, Bromley A, Shields M, Cardwell C. A meta-analysis of the association between Caesarean section and childhood asthma. Clinical & Experimental Allergy. 2008;38(4):629–33.CrossRef
25.
go back to reference Negele K, Heinrich J, Borte M, Berg A, Schaaf B, Lehmann I, et al. Mode of delivery and development of atopic disease during the first 2 years of life. Pediatr Allergy Immunol. 2004;15(1):48–54.CrossRefPubMed Negele K, Heinrich J, Borte M, Berg A, Schaaf B, Lehmann I, et al. Mode of delivery and development of atopic disease during the first 2 years of life. Pediatr Allergy Immunol. 2004;15(1):48–54.CrossRefPubMed
26.
go back to reference Renz-Polster H, David M, Buist A, Vollmer W, O'Connor E, Frazier E, et al. Caesarean section delivery and the risk of allergic disorders in childhood. Clinical & Experimental Allergy. 2005;35(11):1466–72.CrossRef Renz-Polster H, David M, Buist A, Vollmer W, O'Connor E, Frazier E, et al. Caesarean section delivery and the risk of allergic disorders in childhood. Clinical & Experimental Allergy. 2005;35(11):1466–72.CrossRef
27.
go back to reference Eggesbø M, Botten G, Stigum H, Nafstad P, Magnus P. Is delivery by cesarean section a risk factor for food allergy? J Allergy Clin Immunol. 2003;112(2):420–6.CrossRefPubMed Eggesbø M, Botten G, Stigum H, Nafstad P, Magnus P. Is delivery by cesarean section a risk factor for food allergy? J Allergy Clin Immunol. 2003;112(2):420–6.CrossRefPubMed
28.
go back to reference Vatanen T, Kostic AD, d’Hennezel E, Siljander H, Franzosa EA, Yassour M, et al. Variation in microbiome LPS immunogenicity contributes to autoimmunity in humans. Cell. 2016;165(4):842–53.CrossRefPubMedPubMedCentral Vatanen T, Kostic AD, d’Hennezel E, Siljander H, Franzosa EA, Yassour M, et al. Variation in microbiome LPS immunogenicity contributes to autoimmunity in humans. Cell. 2016;165(4):842–53.CrossRefPubMedPubMedCentral
29.
go back to reference Underwood MA, Kalanetra KM, Bokulich NA, Lewis ZT, Mirmiran M, Tancredi DJ, Mills DA: A Comparison of Two Probiotic Strains of Bifidobacteria in Premature Infants. J Pediatr. 2013;163(6):1585-91. Underwood MA, Kalanetra KM, Bokulich NA, Lewis ZT, Mirmiran M, Tancredi DJ, Mills DA: A Comparison of Two Probiotic Strains of Bifidobacteria in Premature Infants. J Pediatr. 2013;163(6):1585-91.
30.
go back to reference Håkansson S, Axemo P, Bremme K, Bryngelsson A-L, Carlsson Wallin M, Ekström C-M, et al. Group B streptococcal carriage in Sweden: a national study on risk factors for mother and infant colonisation. Acta Obstet Gynecol Scand. 2008;87(1):50–8.CrossRefPubMed Håkansson S, Axemo P, Bremme K, Bryngelsson A-L, Carlsson Wallin M, Ekström C-M, et al. Group B streptococcal carriage in Sweden: a national study on risk factors for mother and infant colonisation. Acta Obstet Gynecol Scand. 2008;87(1):50–8.CrossRefPubMed
31.
go back to reference Penders J, Vink C, Driessen C, London N, Thijs C, Stobberingh EE. Quantification of Bifidobacterium spp., Escherichia coli and Clostridium Difficile in faecal samples of breast-fed and formula-fed infants by real-time PCR. FEMS Microbiol Lett. 2005;243(1):141–7.CrossRefPubMed Penders J, Vink C, Driessen C, London N, Thijs C, Stobberingh EE. Quantification of Bifidobacterium spp., Escherichia coli and Clostridium Difficile in faecal samples of breast-fed and formula-fed infants by real-time PCR. FEMS Microbiol Lett. 2005;243(1):141–7.CrossRefPubMed
32.
go back to reference Bekkali N, Hamers SL, Reitsma JB, Van Toledo L, Benninga MA. Infant stool form scale: development and results. J Pediatr. 2009;154(4):521–6. e521CrossRefPubMed Bekkali N, Hamers SL, Reitsma JB, Van Toledo L, Benninga MA. Infant stool form scale: development and results. J Pediatr. 2009;154(4):521–6. e521CrossRefPubMed
33.
go back to reference Wessel MA, Cobb JC, Jackson EB, HARRIS GS, Detwiler AC. Paroxysmal fussing in infancy, sometimes called" colic". Pediatrics. 1954;14(5):421–35.PubMed Wessel MA, Cobb JC, Jackson EB, HARRIS GS, Detwiler AC. Paroxysmal fussing in infancy, sometimes called" colic". Pediatrics. 1954;14(5):421–35.PubMed
34.
go back to reference Hoy-Schulz YE, Jannat K, Roberts T, Zaidi SH, Unicomb L, Luby S, et al. Safety and acceptability of lactobacillus reuteri DSM 17938 and Bifidobacterium longum subspecies infantis 35624 in Bangladeshi infants: a phase I randomized clinical trial. BMC Complement Altern Med. 2016;16(1):1. Hoy-Schulz YE, Jannat K, Roberts T, Zaidi SH, Unicomb L, Luby S, et al. Safety and acceptability of lactobacillus reuteri DSM 17938 and Bifidobacterium longum subspecies infantis 35624 in Bangladeshi infants: a phase I randomized clinical trial. BMC Complement Altern Med. 2016;16(1):1.
35.
go back to reference Kalliomäki M, Salminen S, Arvilommi H, Kero P, Koskinen P, Isolauri E. Probiotics in primary prevention of atopic disease: a randomised placebo-controlled trial. Lancet. 2001;357(9262):1076–9.CrossRefPubMed Kalliomäki M, Salminen S, Arvilommi H, Kero P, Koskinen P, Isolauri E. Probiotics in primary prevention of atopic disease: a randomised placebo-controlled trial. Lancet. 2001;357(9262):1076–9.CrossRefPubMed
36.
go back to reference Weaver LT, Ewing G, Taylor LC. The bowel habit of milk-fed infants. J Pediatr Gastroenterol Nutr. 1988;7(4):568–71.CrossRefPubMed Weaver LT, Ewing G, Taylor LC. The bowel habit of milk-fed infants. J Pediatr Gastroenterol Nutr. 1988;7(4):568–71.CrossRefPubMed
37.
go back to reference Shrago LC, Reifsnider E, Insel K. The neonatal bowel output study: indicators of adequate breast milk intake in neonates. Pediatr Nurs. 2006;32(3):195.PubMed Shrago LC, Reifsnider E, Insel K. The neonatal bowel output study: indicators of adequate breast milk intake in neonates. Pediatr Nurs. 2006;32(3):195.PubMed
38.
go back to reference Çamurdan AD, Beyazova U, Özkan S, Tunç VT. Defecation patterns of the infants mainly breastfed from birth till the 12th month: prospective cohort study. Turk J Gastroenterol. 2014;25(1):1–5.CrossRefPubMed Çamurdan AD, Beyazova U, Özkan S, Tunç VT. Defecation patterns of the infants mainly breastfed from birth till the 12th month: prospective cohort study. Turk J Gastroenterol. 2014;25(1):1–5.CrossRefPubMed
39.
go back to reference Tham E, Nathan R, Davidson G, Moore D. Bowel habits of healthy Australian children aged 0-2 years. J Paediatr Child Health. 1996;32(6):504–7.CrossRefPubMed Tham E, Nathan R, Davidson G, Moore D. Bowel habits of healthy Australian children aged 0-2 years. J Paediatr Child Health. 1996;32(6):504–7.CrossRefPubMed
40.
go back to reference Fontana M, Bianchi C, Cataldo F, Nibali SC, Cucchiara S, Casali L, et al. Bowel frequency in healthy children. Acta Paediatr. 1989;78(5):682–4.CrossRef Fontana M, Bianchi C, Cataldo F, Nibali SC, Cucchiara S, Casali L, et al. Bowel frequency in healthy children. Acta Paediatr. 1989;78(5):682–4.CrossRef
41.
go back to reference Nyhan WL. Stool frequency of normal infants in the first week of life. Pediatrics. 1952;10(4):414–25.PubMed Nyhan WL. Stool frequency of normal infants in the first week of life. Pediatrics. 1952;10(4):414–25.PubMed
42.
go back to reference Tunc VT, Camurdan AD, İlhan MN, Sahin F, Beyazova U. Factors associated with defecation patterns in 0–24-month-old children. Eur J Pediatr. 2008;167(12):1357–62.CrossRefPubMed Tunc VT, Camurdan AD, İlhan MN, Sahin F, Beyazova U. Factors associated with defecation patterns in 0–24-month-old children. Eur J Pediatr. 2008;167(12):1357–62.CrossRefPubMed
43.
go back to reference Vandeputte D, Falony G, Vieira-Silva S, Tito RY, Joossens M, Raes J. Stool consistency is strongly associated with gut microbiota richness and composition, enterotypes and bacterial growth rates. Gut. 2015;65(1):57–62. doi:10.1136/gutjnl-2015-309618. Vandeputte D, Falony G, Vieira-Silva S, Tito RY, Joossens M, Raes J. Stool consistency is strongly associated with gut microbiota richness and composition, enterotypes and bacterial growth rates. Gut. 2015;65(1):57–62. doi:10.​1136/​gutjnl-2015-309618.
44.
go back to reference Fukuda S, Toh H, Hase K, Oshima K, Nakanishi Y, Yoshimura K, et al. Bifidobacteria can protect from enteropathogenic infection through production of acetate. Nature. 2011;469(7331):543–7.CrossRefPubMed Fukuda S, Toh H, Hase K, Oshima K, Nakanishi Y, Yoshimura K, et al. Bifidobacteria can protect from enteropathogenic infection through production of acetate. Nature. 2011;469(7331):543–7.CrossRefPubMed
45.
go back to reference Dong P, Yang Y. Wang W-p: the role of intestinal bifidobacteria on immune system development in young rats. Early Hum Dev. 2010;86(1):51–8.CrossRefPubMed Dong P, Yang Y. Wang W-p: the role of intestinal bifidobacteria on immune system development in young rats. Early Hum Dev. 2010;86(1):51–8.CrossRefPubMed
46.
go back to reference Crockenberg SB, Smith P. Antecedents of mother-infant interaction and infant irritability in the first three months of life. Infant Behavior and Development. 1982;5(2–4):105–19.CrossRef Crockenberg SB, Smith P. Antecedents of mother-infant interaction and infant irritability in the first three months of life. Infant Behavior and Development. 1982;5(2–4):105–19.CrossRef
47.
go back to reference Russo M, Martinelli M, Sciorio E, Botta C, Miele E, Vallone G, et al. Stool consistency, but not frequency, correlates with total gastrointestinal transit time in children. J Pediatr. 2013;162(6):1188–92.CrossRefPubMed Russo M, Martinelli M, Sciorio E, Botta C, Miele E, Vallone G, et al. Stool consistency, but not frequency, correlates with total gastrointestinal transit time in children. J Pediatr. 2013;162(6):1188–92.CrossRefPubMed
Metadata
Title
Safety and tolerability of Bifidobacterium longum subspecies infantis EVC001 supplementation in healthy term breastfed infants: a phase I clinical trial
Authors
Jennifer T. Smilowitz
Jackelyn Moya
Melissa A. Breck
Chelsea Cook
Annette Fineberg
Kathleen Angkustsiri
Mark A. Underwood
Publication date
01-12-2017
Publisher
BioMed Central
Published in
BMC Pediatrics / Issue 1/2017
Electronic ISSN: 1471-2431
DOI
https://doi.org/10.1186/s12887-017-0886-9

Other articles of this Issue 1/2017

BMC Pediatrics 1/2017 Go to the issue