# Bifidobacterium supplementation maintains gut microbiota stability and enhances well-being during short-term travel

**Authors:** Long Wang, Yue Yu, Xiaxian Shen, Xiaohui Li, Danni Wang, Yue Zhai, Wei Jiang, Wei Zhao, Qinghua Yu, Min-Tze Liong, Dongbo Chen, Ai Zhao

PMC · DOI: 10.3389/fnut.2026.1724829 · Frontiers in Nutrition · 2026-02-12

## TL;DR

Taking a Bifidobacterium probiotic during short international travel helps maintain gut health and improves well-being, sleep, and reduces symptoms like fatigue and anxiety.

## Contribution

A randomized trial showing that Bifidobacterium probiotics maintain gut microbiota stability and enhance well-being during travel.

## Key findings

- Probiotic group maintained microbial diversity and prevented harmful taxa enrichment.
- Probiotic users reported fewer symptoms like sore throat, fatigue, and improved sleep and well-being.
- Functional analysis showed increased vitamin biosynthesis and reduced antibiotic resistance genes.

## Abstract

International travel exposes individuals to abrupt environmental, dietary, and circadian changes that can disturb gut microbiota and overall well-being. While probiotics are known to support gastrointestinal and systemic health, their effects during short-term travel remain incompletely characterized in randomized trials.

This randomized, double-blind, placebo-controlled study investigated whether a multi-strain Bifidobacterium probiotic could maintain gut microbiota stability and support health during a five-day trip from China to Japan. Forty healthy adults were randomly assigned to receive either probiotic (n = 22) or placebo (n = 18) daily from Day 1 to Day 4. Stool samples collected before departure (Day 0) and after return (Day 5) were analyzed by metagenomic sequencing, quantitative PCR, and fecal secretory immunoglobulin A (sIgA) assays. Participants completed validated questionnaires on gastrointestinal and respiratory symptoms, sleep quality (PSQI), anxiety (GAD-7), and well-being (WHO-5).

Compared with placebo, participants receiving the probiotic showed maintenance of microbial diversity (Chao1 and Fisher indices, both p = 0.044), prevented enrichment of potentially harmful taxa (Bilophila, Flavonifractor), and increased Bifidobacterium abundance. Clinically, the probiotic group reported fewer respiratory and systemic symptoms, including sore throat (p = 0.034) and fatigue (p = 0.043). Sleep quality also improved, with longer sleep duration (p = 0.023), fewer total occurrence days of PSQI >5 (p = 0.009), lower anxiety scores (p = 0.001) and higher WHO-5 well-being scores (p = 0.041). Functional profiling showed up-regulation of vitamin biosynthesis pathways (folate, biotin, retinol) and decreased antibiotic resistance gene prevalence.

Short-term probiotic administration demonstrated gut microbiota resilience and improved physiological and psychological stability during travel. Probiotics may serve as an accessible strategy to support well-being under transient environmental and lifestyle stress.

ClinicalTrials.gov, identifier NCT07163819.

## Full-text entities

- **Genes:** ABL2 (ABL proto-oncogene 2, non-receptor tyrosine kinase) [NCBI Gene 27] {aka ABLL, ARG}, CYP4F3 (cytochrome P450 family 4 subfamily F member 3) [NCBI Gene 4051] {aka CPF3, CYP4F, CYPIVF3, LTB4H}, CD79A (CD79a molecule) [NCBI Gene 973] {aka IGA, IGAlpha, MB-1, MB1}
- **Diseases:** symptoms (MESH:D012816), Respiratory, gastrointestinal, and systemic symptoms (MESH:D012818), viral (MESH:D014777), sore throat (MESH:D010612), Generalized Anxiety Disorder (MESH:C000726808), gastrointestinal discomfort (MESH:D005767), bile-acid (MESH:C567652), infection (MESH:D007239), inflammatory bowel disease (MESH:D015212), irritable bowel syndrome (MESH:D043183), allergy (MESH:D004342), constipation (MESH:D003248), intestinal disturbances (MESH:D007410), bloating (MESH:C535647), GAD-7 (MESH:C537955), inflammation (MESH:D007249), antibiotic (MESH:D004761), Sleep (MESH:D012893), dysbiosis (MESH:D064806), Anxiety (MESH:D001007), abdominal pain (MESH:D015746), mood disturbances (MESH:D019964), loose (MESH:D007594), TD (MESH:D003967), fatigue (MESH:D005221), systemic disease (MESH:D034721), anxiety disorder (MESH:D001008)
- **Chemicals:** tetA (MESH:D014266), bile acid (MESH:D001647), B. breve M-16V (-), tetracycline (MESH:D013752), thiamine (MESH:D013831), amino acid (MESH:D000596), macrolide (MESH:D018942), Butyrate (MESH:D002087), streptogramin B (MESH:D025381), nicotinate (MESH:D009525), carbohydrate (MESH:D002241), oil (MESH:D009821), CoA (MESH:D003065), vitamin B5 (MESH:D010205), ubiquinone (MESH:D014451), agarose (MESH:D012685), lipid (MESH:D008055), B9 (MESH:C014499), anthocyanins (MESH:D000872), quinone (MESH:C004532), acetate (MESH:D000085), vitamin B6 (MESH:D025101), beta-lactam (MESH:D047090), SCFA (MESH:D005232), folate (MESH:D005492), flavonoids (MESH:D005419), maltodextrin (MESH:C008315), cortisol (MESH:D006854), lincosamides (MESH:D055231), stilbenoids (MESH:D013267), nicotinamide (MESH:D009536), retinol (MESH:D014801), terpenoid (MESH:D013729), indole alkaloids (MESH:D026121), biotin (MESH:D001710)
- **Species:** Lachnospira (genus) [taxon 28050], Bifidobacterium (genus) [taxon 1678], Homo sapiens (human, species) [taxon 9606], Flavonifractor (genus) [taxon 946234], Anaerostipes (genus) [taxon 207244], Anaerobutyricum (genus) [taxon 2569097], gut metagenome (species) [taxon 749906], Bifidobacterium longum (species) [taxon 216816], Faecalibacterium (genus) [taxon 216851], Eubacterium (genus) [taxon 1730], Phocaeicola (genus) [taxon 909656], Actinomyces (genus) [taxon 1654], Enterococcus (genus) [taxon 1350], Romboutsia (genus) [taxon 1501226]

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## Figures

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## References

55 references — full list in the complete paper: https://tomesphere.com/paper/PMC12935942/full.md

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Source: https://tomesphere.com/paper/PMC12935942