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Peer-reviewedCC BY-NC-NDAMB Express

Combined nano-hypericin antimicrobial photodynamic therapy and postbiotic on Streptococcus mutans.

4 affiliations
  1. 1Faculty of Dentistry, Tehran Medical Science, Islamic Azad University, Tehran, Iran.
  2. 2Dental Research Center, Dentistry Research Institute, Tehran University of Medical Sciences, Tehran, Iran. [email protected].
  3. 3Department of Oral and Maxillofacial Medicine, TeMS.C., Islamic Azad University, Tehran, Iran. [email protected].
  4. 4Department of Microbiology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.

Abstract

Dental caries is a prevalent microbial disease, with Streptococcus mutans as a major pathogen. Increasing antibiotic resistance highlights the need for alternative, non-antibiotic strategies. This study evaluated the antimicrobial and anti-virulence potential of nano-hypericin (nHyp)-mediated antimicrobial photodynamic therapy (aPDT) combined with Lactobacillus casei-derived postbiotic (PSLC). nHyp was synthesized and characterized by transmission electron microscopy, UV-Vis spectroscopy, and dynamic light scattering, confirming quasi-spherical nanoparticles (~ 47 nm). PSLC was purified via acid precipitation and chemically profiled by gas chromatography-mass spectrometry, revealing diketopiperazines, fatty acids, hydrocarbons, and phenolic compounds. Planktonic S. mutans were treated with nHyp (1.9-1000 µg/mL) ± blue laser irradiation (450 ± 5 nm, 1-5 min), alone or combined with PSLC at 1/2 × MIC (32 µg/mL). Bacterial viability was measured by colony forming unit (CFU)/mL, and gtfB expression quantified by qRT-PCR. nHyp-mediated aPDT induced dose- and time-dependent reductions in bacterial viability (up to 81%), further enhanced by PSLC (up to 90.5%). Sub-lethal aPDT (15.6 µg/mL + 2 min) downregulated gtfB 4.25-fold, whereas combination with PSLC achieved 7.86-fold suppression, indicating inhibition of glucan synthesis relevant to biofilm formation. These findings demonstrate that nHyp-mediated aPDT combined with PSLC enhances antimicrobial and anti-virulence effects under in vitro conditions, representing a promising dual-mechanism, antibiotic-free approach to modulate cariogenic bacterial pathogenicity.

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BibTeX
@article{ghasemi2026combined,
  title = {{Combined nano-hypericin antimicrobial photodynamic therapy and postbiotic on Streptococcus mutans.}},
  author = {Narges Ghasemi and Maryam Pourhajibagher and Arash Azizi and Abbas Bahador},
  journal = {AMB Express},
  year = {2026},
  month = jul,
  doi = {10.1186/s13568-026-02097-3},
  url = {https://europepmc.org/article/MED/42955588},
  note = {CC BY-NC-ND},
}
RIS
TY  - JOUR
TI  - Combined nano-hypericin antimicrobial photodynamic therapy and postbiotic on Streptococcus mutans.
AU  - Narges Ghasemi
AU  - Maryam Pourhajibagher
AU  - Arash Azizi
AU  - Abbas Bahador
PY  - 2026
DA  - 2026/07/01
JO  - AMB Express
DO  - 10.1186/s13568-026-02097-3
UR  - https://europepmc.org/article/MED/42955588
AB  - Dental caries is a prevalent microbial disease, with Streptococcus mutans as a major pathogen. Increasing antibiotic resistance highlights the need for alternative, non-antibiotic strategies. This study evaluated the antimicrobial and anti-virulence potential of nano-hypericin (nHyp)-mediated antimicrobial photodynamic therapy (aPDT) combined with Lactobacillus casei-derived postbiotic (PSLC). nHyp was synthesized and characterized by transmission electron microscopy, UV-Vis spectroscopy, and dynamic light scattering, confirming quasi-spherical nanoparticles (~ 47 nm). PSLC was purified via acid precipitation and chemically profiled by gas chromatography-mass spectrometry, revealing diketopiperazines, fatty acids, hydrocarbons, and phenolic compounds. Planktonic S. mutans were treated with nHyp (1.9-1000 µg/mL) ± blue laser irradiation (450 ± 5 nm, 1-5 min), alone or combined with PSLC at 1/2 × MIC (32 µg/mL). Bacterial viability was measured by colony forming unit (CFU)/mL, and gtfB expression quantified by qRT-PCR. nHyp-mediated aPDT induced dose- and time-dependent reductions in bacterial viability (up to 81%), further enhanced by PSLC (up to 90.5%). Sub-lethal aPDT (15.6 µg/mL + 2 min) downregulated gtfB 4.25-fold, whereas combination with PSLC achieved 7.86-fold suppression, indicating inhibition of glucan synthesis relevant to biofilm formation. These findings demonstrate that nHyp-mediated aPDT combined with PSLC enhances antimicrobial and anti-virulence effects under in vitro conditions, representing a promising dual-mechanism, antibiotic-free approach to modulate cariogenic bacterial pathogenicity.
SN  - 2191-0855
ER  -