<i>In Vitro</i> and <i>In Vivo</i> Safety Evaluation of <i>Streptococcus salivarius</i> eK12, a Genetically Modified Dietary Probiotic Derived from the Oral Probiotic <i>S. salivarius</i> K12

Group A <i>Streptococcus</i> (GAS) pharyngitis is a common and recurrent childhood illness, usually treated with antibiotics. While effective, repeated antibiotic use contributes to antimicrobial resistance, disrupts host microbiota, and increases adverse effects. <i>Streptococcus salivarius</i> K12 is an extensively studied probiotic for oral health, particularly for reducing the incidence of GAS pharyngotonsillitis. A modified version, <i>S. salivarius</i> eK12, has recently been developed from the wild-type K12 through genetic modification to enhance anti-GAS activity. However, its safety and tolerability have not previously been evaluated, and this study provides the first systematic assessment of eK12 under OECD-guided toxicological frameworks. Genotoxicity was assessed through the bacterial reverse mutation assay (OECD 471, Ames test) in five <i>Salmonella typhimurium</i> strains, with and without metabolic activation. Acute oral toxicity was examined in female Wistar rats at a limit dose of 2,000 mg/kg (~2 × 10<sup>11</sup> CFU/kg) (OECD 423). Sub-chronic safety was investigated in a 90-day repeated-dose oral toxicity study (OECD 408) using Sprague Dawley rats randomized to vehicle, low, mid, or high eK12 dose groups, with additional recovery cohorts (vehicle, high dose) observed for 28 days post-treatment. Results showed no mutagenic activity, no mortality, and no treatment-related abnormalities in clinical, hematological, biochemical, or histopathological parameters. Minor fluctuations were incidental and non-dose dependent. Recovery groups confirmed the absence of delayed or persistent toxicity. These findings indicate that eK12 is potentially non-mutagenic, non-toxic, and well tolerated, with a NOAEL of 2,000 mg/kg/day (~2 × 10<sup>11</sup> CFU/kg/day), retaining the favorable safety profile of its parental strain K12 and supporting its further development.

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Journal
Journal of Microbiology and Biotechnology
Published
2025-12-09
DOI
https://doi.org/10.4014/jmb.2509.09016
Primary Topic
Probiotics and Fermented Foods
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article
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article

In Vitro and In Vivo Safety Evaluation of Streptococcus salivarius eK12, a Genetically Modified Dietary Probiotic Derived from the Oral Probiotic S. salivarius K12

V. Gayathri, Ikram Uddin Ujjan, Maria Laura Tanda, Amjad Khan et al.
Journal of Microbiology and Biotechnology
Probiotics and Fermented Foods
article

In Vitro and In Vivo Safety Evaluation of Streptococcus salivarius eK12, a Genetically Modified Dietary Probiotic Derived from the Oral Probiotic S. salivarius K12

V. Gayathri, Ikram Uddin Ujjan, Maria Laura Tanda, Amjad Khan, Francesco Di Pierro, Nicola Zerbinati, Alexander Bertuccioli, Ali Akbar Bugti, Massimiliano Cazzaniga, Aasiya Bano, Yasmeen Gull, Nasrin Mumtaz, Kuppusamy Kalaiselvan, Bahrudeen Ashif, Logeshwari Jeyakumar, Gopikrishnan Gopalakrishnan
article en

Abstract

Group A <i>Streptococcus</i> (GAS) pharyngitis is a common and recurrent childhood illness, usually treated with antibiotics. While effective, repeated antibiotic use contributes to antimicrobial resistance, disrupts host microbiota, and increases adverse effects. <i>Streptococcus salivarius</i> K12 is an extensively studied probiotic for oral health, particularly for reducing the incidence of GAS pharyngotonsillitis. A modified version, <i>S. salivarius</i> eK12, has recently been developed from the wild-type K12 through genetic modification to enhance anti-GAS activity. However, its safety and tolerability have not previously been evaluated, and this study provides the first systematic assessment of eK12 under OECD-guided toxicological frameworks. Genotoxicity was assessed through the bacterial reverse mutation assay (OECD 471, Ames test) in five <i>Salmonella typhimurium</i> strains, with and without metabolic activation. Acute oral toxicity was examined in female Wistar rats at a limit dose of 2,000 mg/kg (~2 × 10<sup>11</sup> CFU/kg) (OECD 423). Sub-chronic safety was investigated in a 90-day repeated-dose oral toxicity study (OECD 408) using Sprague Dawley rats randomized to vehicle, low, mid, or high eK12 dose groups, with additional recovery cohorts (vehicle, high dose) observed for 28 days post-treatment. Results showed no mutagenic activity, no mortality, and no treatment-related abnormalities in clinical, hematological, biochemical, or histopathological parameters. Minor fluctuations were incidental and non-dose dependent. Recovery groups confirmed the absence of delayed or persistent toxicity. These findings indicate that eK12 is potentially non-mutagenic, non-toxic, and well tolerated, with a NOAEL of 2,000 mg/kg/day (~2 × 10<sup>11</sup> CFU/kg/day), retaining the favorable safety profile of its parental strain K12 and supporting its further development.

Journal of Microbiology and BiotechnologyVol. 35
University of Insubria (IT), Liaquat University of Medical & Health Sciences (PK), Pondicherry University (IN), University of Urbino (IT), Sri Ramachandra Institute of Higher Education and Research (IN), John Radcliffe Hospital (GB), Farooq Hospital (PK), University of Oxford (GB), Velleja Research (IT), Abdus Salam Centre for Physics (PK), Centre for Inflammation Research (GB), Ghaem Hospital (IR), University of Edinburgh (GB)
Openalex Percentile: Top 54%
Probiotics and Fermented Foods
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