# Multi-Model Longevity Assays Reveal Lifespan- and Healthspan-Promoting Effects of Bacillus subtilis WTC019

**Authors:** Nan Zheng, Zhanlei Fan, Yangzhou Diao, Xiangyu Li, Yan Zhang, Bohui Shi, Jinshan Li, Shouyong Ju

PMC · DOI: 10.3390/microorganisms14020314 · 2026-01-29

## TL;DR

A new strain of Bacillus subtilis, WTC019, extends lifespan and improves health in multiple models, suggesting potential for healthy aging.

## Contribution

Demonstrates the novel strain B. subtilis WTC019 promotes longevity and healthspan across invertebrate, cellular, and mammalian models.

## Key findings

- B. subtilis WTC019 extended C. elegans lifespan by up to 35.36% and reduced age-related mobility decline.
- In human fibroblasts, WTC019 reduced senescence markers by 34% and delayed cellular aging.
- Mice supplemented with WTC019 showed a 5.97-6.05% increase in median lifespan.

## Abstract

Bacillus subtilis is a spore-forming probiotic with an established safety profile, yet its effects on aging-related phenotypes remain incompletely defined. Here, we assessed the lifespan- and healthspan-promoting activity of a novel strain, B. subtilis WTC019, using integrated invertebrate, cellular, and mammalian aging models. In Caenorhabditis elegans, B. subtilis WTC019 significantly extended lifespan, increasing median lifespan by 17.48%, 90% lifespan by 35.36%, and maximum lifespan by 19.07%, and attenuated age-associated locomotor decline. In human skin fibroblasts, B. subtilis WTC019 cell lysate reduced senescence-associated β-galactosidase activity by approximately 34% and altered cell cycle distribution consistent with delayed cellular senescence. Moreover, dietary supplementation with B. subtilis WTC019 significantly prolonged lifespan in C57BL/6J mice, with median lifespan increases of 5.97% in females and 6.05% in males. Together, these results demonstrate that B. subtilis WTC019 promotes lifespan- and healthspan-associated phenotypes across multiple aging models, supporting its potential as a probiotic candidate for healthy aging interventions.

## Linked entities

- **Species:** Caenorhabditis elegans (taxon 6239), Homo sapiens (taxon 9606)

## Full-text entities

- **Diseases:** cytotoxicity (MESH:D064420), death (MESH:D003643), head thrash (MESH:D006258), Alzheimer's disease (MESH:D000544), behavioral impairment (MESH:D001523), HSF (MESH:D012871), injury to (MESH:D014947), gingival inflammation (MESH:D007249)
- **Chemicals:** Clorox (MESH:D012973), MTT (MESH:C070243), penicillin (MESH:D010406), DMEM (-), PI (MESH:D011419), 5-fluorodeoxyuridine (MESH:D005467), DMSO (MESH:D004121), PBS (MESH:D007854), lipid (MESH:D008055), CO2 (MESH:D002245), streptomycin (MESH:D013307), agar (MESH:D000362), phosphate (MESH:D010710), NaOH (MESH:D012972), ethanol (MESH:D000431), NO (MESH:D009569)
- **Species:** Homo sapiens (human, species) [taxon 9606], Porphyromonas gingivalis (species) [taxon 837], Bacillus subtilis subsp. subtilis str. 168 (strain) [taxon 224308], Mus musculus (house mouse, species) [taxon 10090], Caenorhabditis elegans (species) [taxon 6239], Escherichia coli OP50 (strain) [taxon 637912], Escherichia coli (E. coli, species) [taxon 562], Bacillus subtilis (species) [taxon 1423], C. elegans [taxon 328850], Bacillus subtilis TO-A (strain) [taxon 1340494]
- **Cell lines:** C57BL/6J — Mus musculus (Mouse), Transformed cell line (CVCL_C0MW), WTC019 — Homo sapiens (Human), Induced pluripotent stem cell (CVCL_Y803), HSF — Homo sapiens (Human), Finite cell line (CVCL_ZT00), OP50 — Homo sapiens (Human), q11.2) BCR-ABL1, Cancer cell line (CVCL_DG77)

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12943744/full.md

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Source: https://tomesphere.com/paper/PMC12943744