PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
April 11, 2026Microorganisms2 citationsOpen Access

Assessment of the Safety and Potential Probiotic Properties of Lactiplantibacillus plantarum LP28 Based on Whole Genome Sequencing and Phenotypic and Oral Toxicity Analyses

View Full Paper
YLYi-Chu LiaoYCYi-Chen ChengCLChia-Chia Lee

Key Points

  • Assess the safety and probiotic properties of Lactiplantibacillus plantarum LP28 using genomic and toxicity analyses.
  • Whole-genome sequencing of LP28
  • In vitro Ames bacterial mutation assay
  • Chromosomal aberration testing
  • In vivo toxicity evaluations in mice and rats
  • Phenotypic tests for hemolytic activity and antibiotic susceptibility.
  • LP28 showed no hemolytic activity and was susceptible to most antibiotics, excluding kanamycin.
  • No significant toxicity observed in ICR mice or SD rats at a dosage of 2000 mg/kg body weight/day.
  • Whole-genome analysis revealed no antimicrobial resistance genes or harmful virulence factors.
  • Presence of genes related to stress responses and adhesion-confirmed was found in LP28.
  • LP28 has six genes encoding bacteriocin precursor peptides, indicating strong probiotic potential.

Abstract

Lactiplantibacillus plantarum LP28 (LP28), isolated from traditional Taiwanese dried tofu, has been demonstrated to have substantial probiotic potential because it increases the production of short-chain fatty acids (SCFAs) and strengthens anti-inflammatory responses. In this study, the safety of LP28 was assessed using both in vitro and in vivo approaches, including whole-genome sequence analysis, the Ames bacterial reverse mutation assay, a chromosomal aberration test, a rodent peripheral blood micronucleus test, a 28-day subacute oral toxicity assay, and an assessment of hemolytic activity. In vitro phenotypic evaluation revealed that LP28 exhibited no hemolytic activity and was susceptible to all the tested antibiotics except kanamycin. In vivo assessments revealed no significant alterations in reticulocyte counts or micronuclei incidence in ICR mice, and SD rats exhibited no subacute toxicity at an oral LP28 dosage of 2000 mg/kg body weight/day for 28 days. Moreover, a whole-genome sequence analysis of LP28 revealed the absence of antimicrobial resistance genes, harmful virulence factors, and genes associated with biogenic amine synthesis. Additionally, the presence of genes involved in stress responses (e.g., acid, bile salt, heat, osmotic, and oxidative stresses) and adhesion-related genes was confirmed. Furthermore, LP28 contains six genes (plnA, plnE, plnF, plnJ, plnK, and plnN) that encode bacteriocin precursor peptides, suggesting the potential for enhanced probiotic effects through the production of antimicrobial plantaricins. These findings highlight the potential of LP28 as a safe and effective probiotic for human consumption.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Liao et al. (2026) studied this question.

synapsesocial.com/papers/69d9e5d178050d08c1b76051https://doi.org/10.3390/microorganisms14040843
Ask AI
Helpful
Bookmark
Share
View Full Paper