Lactiplantibacillus plantarum ATA-LPC98052 demonstrated favorable in vitro probiotic characteristics, technological stability, gut microbiota-modulating potential, and a favorable subacute safety profile under the tested conditions, though microbiota findings were exploratory and phenotypic MIC testing remains warranted.
Key Findings
Results
ATA-LPC98052 exhibited gamma-hemolysis, indicating it does not lyse red blood cells and poses no hemolytic risk.
Hemolysis testing was conducted as part of in vitro safety characterization.
Gamma-hemolysis (no hemolysis) is a favorable safety characteristic for probiotic candidates.
This result distinguishes the strain from potentially pathogenic alpha- or beta-hemolytic organisms.
Results
ATA-LPC98052 maintained substantial viability under simulated gastric acid conditions, with 60% viability at pH 1.5 and 96% viability at pH 5.0.
Acid tolerance was tested across multiple pH levels including pH 1.5 and pH 5.0.
60% viability was retained at the most extreme acidic condition tested (pH 1.5).
96% viability was maintained at pH 5.0, suggesting strong tolerance at moderately acidic conditions.
These results indicate the strain can survive passage through the stomach.
Results
ATA-LPC98052 demonstrated high bile salt tolerance, with viability ranging from 74% to 82% across 0.1–0.5% bile salt concentrations.
Bile tolerance was evaluated across a range of bile salt concentrations (0.1–0.5%).
Viability ranged from 74% to 82% across all tested concentrations.
These levels simulate conditions encountered in the small intestine.
High bile tolerance supports the strain's potential to survive gut transit.
Results
ATA-LPC98052 showed high adhesion to Caco-2 intestinal epithelial cells exceeding 90%, with negligible cytotoxicity (99% cell viability).
Caco-2 adhesion exceeded 90%, indicating strong potential for gut colonization.
Caco-2 cell viability was 99%, indicating the strain is non-cytotoxic to intestinal epithelial cells.
Caco-2 cells are a standard human intestinal epithelial cell model used in probiotic research.
Results
The lyophilized preparation of ATA-LPC98052 was stable for 15 months, maintaining 9.6 log10 CFU/g.
Storage stability was assessed for the lyophilized (freeze-dried) form of the strain.
The preparation maintained 9.6 log10 CFU/g after 15 months of storage.
This level of stability is relevant for commercial probiotic product development and shelf life.
Results
Repeated oral administration of ATA-LPC98052 to Wistar rats for 28 days caused no mortality and no consistent treatment-related toxicological pattern.
The subacute oral safety study used Wistar rats administered the strain by gavage for 28 days.
The dose was 1.2 × 10¹¹ CFU/kg/day.
The study design incorporated selected principles of OECD Test Guideline 407.
Clinical, hematological, biochemical, organ-weight, and macroscopic endpoints were all evaluated.
No mortality was observed and no consistent treatment-related toxicological pattern was identified.
Results
Longitudinal fecal microbiota analysis showed no significant treatment × time effects on alpha diversity or community structure, and no genus-level association was FDR-significant.
Fecal microbiota was analyzed using 16S rRNA sequencing.
No significant treatment × time interaction effects were observed for alpha diversity metrics.
Bray-Curtis community structure (beta diversity) also showed no significant treatment × time effects.
MaAsLin2 analysis found no genus-level associations that were significant after false discovery rate (FDR) correction.
Authors noted that microbiota findings were exploratory in nature.
Results
Whole genome sequencing (WGS) confirmed ATA-LPC98052 identity as L. plantarum with no contamination detected, and ResFinder found no acquired antimicrobial resistance determinants meeting specified thresholds.
WGS was used for taxonomic confirmation and genomic safety screening.
ResFinder analysis detected no acquired antimicrobial resistance determinants meeting the specified thresholds.
CARD/RGI identified low-identity homologs of qacJ and vanY, described as requiring cautious interpretation.
The authors noted that phenotypic MIC (minimum inhibitory concentration) testing remains warranted despite these genomic findings.
What This Means
This research suggests that a specific probiotic bacterial strain called Lactiplantibacillus plantarum ATA-LPC98052 has favorable safety and functional characteristics that support its potential use as a probiotic ingredient. In laboratory tests, the strain survived simulated stomach acid (retaining 60–96% viability depending on pH) and bile salts (74–82% viability), adhered strongly to intestinal cells (over 90% adhesion), and did not damage those cells (99% cell viability). The freeze-dried preparation also remained stable and potent for 15 months, which is important for commercial products. When given to rats at a high dose every day for 28 days, the strain caused no deaths and no consistent signs of toxicity across blood, organ, and clinical measures.
The study also used advanced genetic sequencing to confirm the strain's identity and screen for potential safety concerns. No acquired antibiotic resistance genes were found at concerning levels, though two low-similarity gene sequences (qacJ and vanY) were flagged as needing further investigation with laboratory-based antibiotic resistance testing. Analysis of the gut bacteria (microbiome) in the rats showed that taking this probiotic did not significantly disrupt the overall balance or diversity of the gut microbial community, which is generally considered a positive safety indicator.
This research suggests that ATA-LPC98052 has the characteristics expected of a safe and functional probiotic candidate, but the authors emphasize that some findings — particularly around antibiotic resistance and gut microbiota effects — are preliminary and require additional testing before definitive conclusions can be drawn. Because probiotic safety is strain-specific, these results apply only to this particular strain and cannot be generalized to other L. plantarum products.
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