Bifidobacterium longum

Bifidobacterium longum
Evidence Level
Limited
4 Clinical Trials
5 Documented Benefits
2/5 Evidence Score

Bifidobacterium longum is a probiotic bacterium that lives in the human gut. Bifidobacteria often dominate the gut of breastfed infants and make up a much smaller share of the adult gut microbiota. Its effects depend on the strain, so results for one strain do not carry over to another. Strain 1714 has been studied for the stress response, sleep and mood in healthy adults, with small or mixed results. Strain 35624 (first named B. infantis 35624) has been studied for abdominal comfort and bloating, and BB536 for bowel regularity in older adults, nasal comfort during pollen season and upper respiratory health in children. Most of these trials were run or funded by the companies that make the strains, and several missed their main goal, so look for a product that names the strain and dose used in the research.

Studied Dose Strain specific. 1714: 1 billion CFU/day in stress and sleep trials, 10 billion in a mood trial. 35624: 100 million CFU/day was the only dose that beat placebo in women with IBS. BB536: 5 billion CFU/day in children, 50 to 100 billion in older adults.
Active Compound Live Bifidobacterium longum (strains 1714, BB536, 35624, others)

Benefits

Stress response and daily stress (1714 strain)

Tested as the 1714 strain. In 22 healthy men given placebo first and then 1 billion CFU/day for 4 weeks each, the probiotic blunted the rise in cortisol and anxiety during a cold-water stress test and lowered daily stress. A 40-person randomized trial saw brain-activity changes but no difference in felt stress, and two larger trials missed their main sleep and mood goals.

Abdominal comfort and bloating (35624 strain)

In 362 women with IBS, 4 weeks of strain 35624 at 100 million CFU/day eased abdominal discomfort, bloating and bowel habits more than placebo, but the lower and higher doses did not beat placebo. In 302 adults with bloating who were not under a doctor's care, 1 billion CFU/day did not ease symptom severity more than placebo, though bloating-free days rose.

Nasal comfort during pollen season (BB536 strain)

In 44 people with Japanese cedar pollen allergy, BB536 taken for 13 weeks of the pollen season led to fewer early dropouts for severe symptoms or medication and lower runny nose, blocked nose and overall symptom scores than placebo. This is one small trial run by researchers at Morinaga, the strain's maker.

Bowel regularity in older adults (BB536 strain)

In 80 older adults (mean age 78) with chronic constipation, 50 billion CFU/day of BB536 for 4 weeks did not beat placebo on the main constipation score (P = 0.074), but stool frequency improved more than on placebo. Several authors were from Morinaga, the strain's maker.

Upper respiratory immune support in children and older adults (BB536 strain)

Tested as the BB536 strain only. In 520 Malaysian preschoolers given 5 billion CFU/day or placebo for 10 months, the BB536 group had fewer respiratory illnesses and 46% shorter sore throats, but only the 219 fully compliant children were analysed, and diarrhoea did not change. In 27 elderly adults, fewer caught influenza or had fever than on placebo over 14 weeks. Morinaga, which makes BB536, co-authored both.

Mechanism of action

1

Gut-brain signaling (proposed)

How strain 1714 might affect stress is not settled. Researchers suspect signals from the gut to the brain through nerves, immune messengers and microbial products. Changes in EEG and MEG brain activity in 1714 trials suggest some effect on the brain, but the pathway has not been shown in people.

2

Human milk oligosaccharide use

The infantis subspecies carries a large gene cluster for breaking down human milk oligosaccharides, sugars in breast milk that the infant cannot digest. This helps explain why it thrives in the gut of breastfed babies.

3

Cross-feeding of butyrate producers

Bifidobacteria ferment fibers and other carbohydrates the body cannot digest. Their products, such as acetate and lactate, can be used by other colon bacteria that make butyrate, the main fuel for the cells lining the colon.

Clinical trials

1
B. longum 1714 and the stress response in healthy men
PubMed

Within-participant, placebo-controlled study. Participants took placebo for 4 weeks and then B. longum 1714 (1 billion CFU/day) for 4 weeks, in that fixed order, with a socially evaluated cold pressor stress test, cognitive tests and resting EEG after each phase. The strain's maker supplied the products. (Allen et al. 2016, Transl Psychiatry)

22 healthy men.

After the probiotic phase, the rise in cortisol and in anxiety during the stress test was smaller and daily reported stress was lower. The authors also saw subtle gains in a visuospatial memory task and changes in frontal EEG. The fixed order (placebo always first) and small size limit how much this shows.

2
B. infantis 35624 in women with IBS: dose-ranging trial
PubMed

Randomized, double-blind, placebo-controlled multicenter trial of encapsulated B. infantis 35624 (now classified as B. longum 35624) at 1 million, 100 million or 10 billion CFU/day for 4 weeks. (Whorwell et al. 2006, Am J Gastroenterol)

362 women with IBS recruited in primary care.

Only the 100 million CFU dose beat placebo on the main outcome, abdominal pain or discomfort, and on bloating, bowel dysfunction, incomplete evacuation, straining, gas and the composite score; global symptom relief beat placebo by more than 20%. The 1 million and 10 billion doses did not differ from placebo, and the 10 billion dose had formulation problems.

3
B. longum BB536 for Japanese cedar pollinosis: randomized trial
PubMed

Randomized, double-blind, placebo-controlled trial of B. longum BB536 during the cedar pollen season, run by researchers at Morinaga, the strain's maker. (Xiao et al. 2006, Clin Exp Allergy)

44 people with Japanese cedar pollinosis, 13 weeks.

Fewer people on BB536 dropped out early because of severe symptoms or allergy medication (P = 0.0057 vs placebo), and rhinorrhea, nasal blockage and composite symptom scores fell more than on placebo. BB536 suppressed the pollen-season rise in plasma TARC, a Th2-related chemokine, while cedar-pollen-specific IgE only tended to rise less.

4
B. longum BB536 for bowel regularity in older adults
PubMed

Randomized, double-blind, placebo-controlled trial of BB536 (50 billion CFU once daily) for 4 weeks. (Takeda et al. 2023, Am J Gastroenterol)

80 adults (79 completed, mean age 77.9) diagnosed with chronic constipation in Japan.

The main outcome, the change in total constipation score versus placebo, was not significant (P = 0.074). Stool frequency improved more than on placebo (P = 0.008), and failure of evacuation tended to improve (P = 0.051). Few side effects were seen. Several authors were from Morinaga.

Side effects and drug interactions

Common Potential side effects

Generally well tolerated in the trials above, with few side effects reported.
Effects are strain and dose specific: in one large trial, only the middle dose of strain 35624 beat placebo.
People who are severely immunocompromised or critically ill should ask a doctor before taking any live probiotic.

Important Drug interactions

Antibiotics can kill live probiotic bacteria; many labels advise taking the probiotic a few hours apart from antibiotic doses.
Immunosuppressive drugs: ask a doctor before using live probiotics.

Frequently asked questions about Bifidobacterium longum

What is Bifidobacterium longum used for?

B. longum is studied for bowel regularity and abdominal comfort, upper respiratory health and the gut-brain axis, with strain 1714 researched for the stress response, sleep and mood. Results depend on the strain.

Does B. longum help with stress or mood?

Strain 1714 has some research suggesting a calmer stress response, but the evidence is small: the best-known study had 22 men and no random order, and two larger trials missed their main sleep and mood goals. Choose a product that names the strain studied.

How much B. longum should I take?

Doses in trials depend on the strain: about 1 billion CFU per day for 1714, 100 million CFU for 35624 and 5 to 100 billion CFU for BB536. Follow the product's label and check that it names the strain.

Is B. longum safe?

It was well tolerated in the trials above. As with all live probiotics, severely immunocompromised or critically ill people should check with a doctor first.

What is Bifidobacterium longum?

Bifidobacterium longum is a probiotic bacterium that lives in the human gut. Bifidobacteria often dominate the gut of breastfed infants and make up a much smaller share of the adult gut microbiota. Its effects depend on the strain, so results for one strain do not carry over to another.

Does Bifidobacterium longum interact with any medications?

Possible interactions include: Antibiotics can kill live probiotic bacteria; many labels advise taking the probiotic a few hours apart from antibiotic doses. Immunosuppressive drugs: ask a doctor before using live probiotics. If you take prescription medication, check with a pharmacist or doctor before using it.

How strong is the scientific evidence for Bifidobacterium longum?

NutraSmarts rates the evidence for Bifidobacterium longum as Limited (2 out of 5). It is backed by 4 study summaries and 14 cited references summarized on this page. A higher rating reflects more, larger, and better-designed human studies.

References(14 citations)

Evidence ratings on NutraSmarts are based on the totality of human clinical research, with emphasis on randomized controlled trials, meta-analyses, and systematic reviews. The references below directly support claims made throughout this page.

  1. Miyamoto S, Yoshimoto S, Katsumata N, Mutoh N, Iwabuchi N, Odamaki T, Asaoka D, Machida S. Bifidobacterium longum BB536 is associated with improvements in gastrointestinal symptoms and odor-related metabolites in microbiota-defined subgroups of male athletes consuming a high-protein diet: exploratory randomized double-blind placebo-controlled trial. J Int Soc Sports Nutr. 2026;23(1):2664664. doi: 10.1080/15502783.2026.2664664.PubMedUsed to support: Exploratory randomized trial in 60 male athletes on a high-protein diet given BB536 (46 billion CFU/day) or placebo for 4 weeks. No differences between groups were found in the whole group; diarrhoea-related scores improved within the BB536 group, and odor-related metabolites fell only in post hoc subgroups. Six authors are Morinaga employees.
  2. Xiao JZ, Kondo S, Yanagisawa N, Takahashi N, Odamaki T, Iwabuchi N, Miyaji K, Iwatsuki K, Togashi H, Enomoto K, Enomoto T. Probiotics in the treatment of Japanese cedar pollinosis: a double-blind placebo-controlled trial. Clin Exp Allergy. 2006;36(11):1425-35. doi: 10.1111/j.1365-2222.2006.02575.x.PubMedUsed to support: Randomized, double-blind, placebo-controlled trial in 44 people with Japanese cedar pollinosis over 13 weeks of the pollen season: fewer early withdrawals for severe symptoms or medication and lower rhinorrhea, nasal blockage and composite symptom scores than placebo; the rise in plasma TARC was suppressed and cedar-specific IgE only tended to rise less. Authors from Morinaga, the maker of BB536.
  3. Lau AS, Yanagisawa N, Hor YY, Lew LC, Ong JS, Chuah LO, Lee YY, Choi SB, Rashid F, Wahid N, Sugahara H, Xiao JZ, Liong MT. Bifidobacterium longum BB536 alleviated upper respiratory illnesses and modulated gut microbiota profiles in Malaysian pre-school children. Benef Microbes. 2018;9(1):61-70. doi: 10.3920/BM2017.0063.PubMedUsed to support: 10-month randomized, double-blind, placebo-controlled trial in 520 healthy Malaysian children aged 2 to 6 given BB536 (5 billion CFU/day) or placebo. In the 219 fully compliant children analysed, the BB536 group had fewer respiratory illnesses and a 46% shorter sore throat duration (P = 0.018), with only marginal effects on fever, runny nose and cough and no effect on diarrhoea. Co-authored by Morinaga staff.
  4. Namba K, Hatano M, Yaeshima T, Takase M, Suzuki K. Effects of Bifidobacterium longum BB536 administration on influenza infection, influenza vaccine antibody titer, and cell-mediated immunity in the elderly. Biosci Biotechnol Biochem. 2010;74(5):939-45. doi: 10.1271/bbb.90749.PubMedUsed to support: 27 elderly adults (mean age 86.7) took BB536 (100 billion CFU/day) for 5 weeks, with a flu vaccine at week 3, and were then randomized to BB536 or placebo for 14 weeks. Fewer contracted influenza or had fever on BB536, and NK cell and neutrophil activity only tended to stay higher. The first author is from Morinaga Milk Industry.
  5. Allen AP, Hutch W, Borre YE, Kennedy PJ, Temko A, Boylan G, Murphy E, Cryan JF, Dinan TG, Clarke G. Bifidobacterium longum 1714 as a translational psychobiotic: modulation of stress, electrophysiology and neurocognition in healthy volunteers. Transl Psychiatry. 2016;6(11):e939. doi: 10.1038/tp.2016.191.PubMedUsed to support: In 22 healthy men given placebo and then B. longum 1714 for 4 weeks each (fixed order), the cortisol and anxiety rise during a cold pressor stress test was smaller and daily stress was lower after the probiotic, with subtle memory and EEG changes. The maker supplied the products and one author worked for it.
  6. Wang H, Braun C, Murphy EF, Enck P. Bifidobacterium longum 1714™ Strain Modulates Brain Activity of Healthy Volunteers During Social Stress. Am J Gastroenterol. 2019;114(7):1152-1162. doi: 10.14309/ajg.0000000000000203.PubMedUsed to support: Randomized, double-blind trial in 40 healthy volunteers given B. longum 1714 or placebo for 4 weeks. The probiotic changed resting and stress-related brain activity on MEG, linked to vitality, but felt social stress rose in all groups with no behavioral difference.
  7. Patterson E, Tan HTT, Groeger D, Andrews M, Buckley M, Murphy EF, Groeger JA. Bifidobacterium longum 1714 improves sleep quality and aspects of well-being in healthy adults: a randomized, double-blind, placebo-controlled clinical trial. Sci Rep. 2024;14(1):3725. doi: 10.1038/s41598-024-53810-w.PubMedUsed to support: In 89 adults with poor sleep, 8 weeks of B. longum 1714 (1 billion CFU/day) did not beat placebo on the main sleep score; the sleep quality component and daytime sleepiness improved faster at 4 weeks, and energy and social functioning were better at 8 weeks. Actigraphy did not change. Sponsored by the strain's owner.
  8. Seamans KM, Patterson E, Holz C, Groeger D, Junnila J, Collins F, Murphy EF, Sorensen K, Dinan TG. Effects of Bifidobacterium longum 1714 on low mood and related symptoms: A randomized, double-blind, placebo-controlled trial. Exp Clin Psychopharmacol. 2026;34(4):341-351. doi: 10.1037/pha0000839.PubMedUsed to support: In 168 adults with mild to moderate low mood, 8 weeks of B. longum 1714 (10 billion CFU/day) did not beat placebo on the main depression score; sleep and secondary mood scores were better at week 4 but not week 8, and vitality stayed better at week 8.
  9. Whorwell PJ, Altringer L, Morel J, Bond Y, Charbonneau D, O'Mahony L, Kiely B, Shanahan F, Quigley EM. Efficacy of an encapsulated probiotic Bifidobacterium infantis 35624 in women with irritable bowel syndrome. Am J Gastroenterol. 2006;101(7):1581-90. doi: 10.1111/j.1572-0241.2006.00734.x.PubMedUsed to support: In 362 women with IBS, 4 weeks of B. infantis 35624 at 100 million CFU/day beat placebo for abdominal pain or discomfort, bloating, bowel dysfunction and global relief; 1 million and 10 billion CFU doses did not differ from placebo.
  10. Ringel-Kulka T, McRorie J, Ringel Y. Multi-Center, Double-Blind, Randomized, Placebo-Controlled, Parallel-Group Study to Evaluate the Benefit of the Probiotic Bifidobacterium infantis 35624 in Non-Patients With Symptoms of Abdominal Discomfort and Bloating. Am J Gastroenterol. 2017;112(1):145-151. doi: 10.1038/ajg.2016.511.PubMedUsed to support: In 302 adults with frequent abdominal discomfort and bloating who were not under medical care, 4 weeks of B. infantis 35624 (1 billion CFU/day) did not reduce symptom severity more than placebo; bloating-free days were more frequent on the probiotic.
  11. Altmann F, Kosma P, O'Callaghan A, Leahy S, Bottacini F, Molloy E, Plattner S, Schiavi E, Gleinser M, Groeger D, Grant R, Rodriguez Perez N, Healy S, Svehla E, Windwarder M, Hofinger A, O'Connell Motherway M, Akdis CA, Xu J, Roper J, van Sinderen D, O'Mahony L. Genome Analysis and Characterisation of the Exopolysaccharide Produced by Bifidobacterium longum subsp. longum 35624™. PLoS One. 2016;11(9):e0162983. doi: 10.1371/journal.pone.0162983.PubMedUsed to support: Genome sequencing showed that strain 35624, formerly named B. longum subsp. infantis, belongs to subspecies longum.
  12. Takeda T, Asaoka D, Nojiri S, Yanagisawa N, Nishizaki Y, Osada T, Koido S, Nagahara A, Katsumata N, Odamaki T, Xiao JZ, Ohkusa T, Sato N. Usefulness of Bifidobacterium longum BB536 in Elderly Individuals With Chronic Constipation: A Randomized Controlled Trial. Am J Gastroenterol. 2023;118(3):561-568. doi: 10.14309/ajg.0000000000002028.PubMedUsed to support: In 80 older adults with chronic constipation, 4 weeks of BB536 (50 billion CFU/day) did not beat placebo on the main constipation score (P = 0.074), but stool frequency improved more than on placebo (P = 0.008).
  13. Sela DA, Chapman J, Adeuya A, Kim JH, Chen F, Whitehead TR, Lapidus A, Rokhsar DS, Lebrilla CB, German JB, Price NP, Richardson PM, Mills DA. The genome sequence of Bifidobacterium longum subsp. infantis reveals adaptations for milk utilization within the infant microbiome. Proc Natl Acad Sci U S A. 2008;105(48):18964-9. doi: 10.1073/pnas.0809584105.PubMedUsed to support: Genome study showing that B. longum subsp. infantis carries a 43 kbp gene cluster for using human milk oligosaccharides, and that the breastfed infant gut is often dominated by bifidobacteria.
  14. Rivière A, Selak M, Lantin D, Leroy F, De Vuyst L. Bifidobacteria and Butyrate-Producing Colon Bacteria: Importance and Strategies for Their Stimulation in the Human Gut. Front Microbiol. 2016;7:979. doi: 10.3389/fmicb.2016.00979.PubMedUsed to support: Review describing cross-feeding between bifidobacteria and butyrate-producing colon bacteria, butyrate as the main energy source for colon cells, and the drop in bifidobacteria from up to 90% of the colon microbiota in breastfed infants to under 5% in adults.