A Thermophilic Bacteriophage TP-84 Surrogate System for Validating Photocatalytic and Ultraviolet Inactivation of Airborne Viruses, Including SARS-CoV-2
- 1Department of Molecular Biotechnology, Faculty of Chemistry, University of Gdańsk, Wita Stwosza 63, 80-308 Gdańsk, Poland
- 2Department of Biomedical Chemistry, Faculty of Physical Education, Gdańsk University of Physical Education and Sport, Górskiego 1, 80-336 Gdańsk, Poland
- 3Department of Environmental Technology, Faculty of Chemistry, University of Gdańsk, Wita Stwosza 63, 80-308 Gdańsk, Poland
Abstract
The airborne transmission of SARS-CoV-2 has renewed interest in engineering controls for indoor air; photocatalytic oxidation over titanium dioxide (TiO2) under ultraviolet (UV) light is an attractive, reagent-free basis for such controls. Rational development requires a biosafe, quantifiable challenge organism usable at biosafety level 1 (BSL-1). We validated the thermophilic bacteriophage TP-84 (host Geobacillus stearothermophilus) as a surrogate for airborne viruses, characterising its stability, aerosolisation, recovery from photocatalytic supports and inactivation on TiO2 surfaces under UVA, UVC and UVA + UVC by a reference-normalised mass balance. TP-84 was stable in a simulated saliva matrix, survived ultrasonic nebulisation, and was recovered from porous ceramic supports at 66.0–91.7%. Five minutes of UV on TiO2 surfaces—UVC (254 nm, 540 mJ cm−2) or combined UVA + UVC (2040 mJ cm−2)—inactivated 87.4–89.4% and 61.6–76.5% of phage, respectively; bulk liquid was strongly protective (94.6–97.5% recovery), whereas desiccation reduced recovery to 4.3–16%. Flow-through aerosol assays provided a device test bed. Because TP-84 is a hardy, non-enveloped dsDNA virus, these values are conservative lower bounds that must not be equated with SARS-CoV-2 efficacy; validation with an enveloped surrogate and authentic virus is the next step.
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BibTeX
@article{sobolewski2026thermophilic,
title = {{A Thermophilic Bacteriophage TP-84 Surrogate System for Validating Photocatalytic and Ultraviolet Inactivation of Airborne Viruses, Including SARS-CoV-2}},
author = {Ireneusz Sobolewski and Beata Łubkowska and Paweł Mazierski and Anna Gołąbiewska and Adriana Zaleska-Medyńska and Piotr M. Skowron},
journal = {International Journal of Molecular Sciences},
year = {2026},
month = oct,
doi = {10.3390/ijms27209271},
url = {https://www.mdpi.com/1422-0067/27/20/9271},
note = {CC BY 4.0},
}
RIS
TY - JOUR
TI - A Thermophilic Bacteriophage TP-84 Surrogate System for Validating Photocatalytic and Ultraviolet Inactivation of Airborne Viruses, Including SARS-CoV-2
AU - Ireneusz Sobolewski
AU - Beata Łubkowska
AU - Paweł Mazierski
AU - Anna Gołąbiewska
AU - Adriana Zaleska-Medyńska
AU - Piotr M. Skowron
PY - 2026
DA - 2026/10/01
JO - International Journal of Molecular Sciences
DO - 10.3390/ijms27209271
UR - https://www.mdpi.com/1422-0067/27/20/9271
AB - The airborne transmission of SARS-CoV-2 has renewed interest in engineering controls for indoor air; photocatalytic oxidation over titanium dioxide (TiO2) under ultraviolet (UV) light is an attractive, reagent-free basis for such controls. Rational development requires a biosafe, quantifiable challenge organism usable at biosafety level 1 (BSL-1). We validated the thermophilic bacteriophage TP-84 (host Geobacillus stearothermophilus) as a surrogate for airborne viruses, characterising its stability, aerosolisation, recovery from photocatalytic supports and inactivation on TiO2 surfaces under UVA, UVC and UVA + UVC by a reference-normalised mass balance. TP-84 was stable in a simulated saliva matrix, survived ultrasonic nebulisation, and was recovered from porous ceramic supports at 66.0–91.7%. Five minutes of UV on TiO2 surfaces—UVC (254 nm, 540 mJ cm−2) or combined UVA + UVC (2040 mJ cm−2)—inactivated 87.4–89.4% and 61.6–76.5% of phage, respectively; bulk liquid was strongly protective (94.6–97.5% recovery), whereas desiccation reduced recovery to 4.3–16%. Flow-through aerosol assays provided a device test bed. Because TP-84 is a hardy, non-enveloped dsDNA virus, these values are conservative lower bounds that must not be equated with SARS-CoV-2 efficacy; validation with an enveloped surrogate and authentic virus is the next step.
SN - 1422-0067
ER -