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UV-C LED wavelength effects on inactivation kinetics, DNA damage and membrane integrity in drinking water indicator bacteria
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  • Published: 03 April 2026

UV-C LED wavelength effects on inactivation kinetics, DNA damage and membrane integrity in drinking water indicator bacteria

  • João Sério1,2,
  • Carolina Santos1,2,
  • Maria Eduarda Martins1,
  • Ana Paula Marques1 nAff3,
  • Carolina Feliciano2,
  • Mónica Serrano2,
  • Adriano O. Henriques2,
  • Maria Teresa Barreto Crespo1,2 &
  • …
  • Vanessa Jorge Pereira1,2 

Scientific Reports (2026) Cite this article

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We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply.

Subjects

  • Biological techniques
  • Biotechnology
  • Environmental sciences
  • Microbiology

Abstract

Ultraviolet (UV) light-emitting diodes (LEDs) have emerged as a promising technology for water disinfection, offering selectable wavelengths that enable more precise targeting of specific cellular components. This study evaluated the inactivation efficiency of water quality indicators with different cell morphologies and envelope organization, Escherichia coli (Gram-negative) and Enterococcus faecium (Gram-positive), including both environmental and culture collection strains, using UV-C LEDs that emit light at 255 nm, 260 nm, 265 nm, 270 nm, and 280 nm. Inactivation kinetics as well as post-exposure repair, under dark and light conditions, were evaluated. Fluorescence microscopy observations and cyclobutane pyrimidine dimer formation were analyzed to elucidate morphological changes and DNA damage. Within the tested range, 265 nm LEDs achieved the highest inactivation rates for E. coli at a given UV fluence, consistent with the DNA absorption maximum in the 260–270 nm region. In contrast, E. faecium showed similar inactivation between 260 and 270 nm. Nevertheless, all tested wavelengths demonstrated high efficacy, achieving up to 6-log inactivation of both culture collection and environmental strains at low UV fluences (below 7 mJ/cm²). E. faecium showed enhanced resilience at lower fluences for all the wavelengths tested. Fluorescence microscopy revealed that both membrane integrity and DNA structure were increasingly affected by higher UV fluences, although signs of DNA damage were more pronounced and detectable even at lower exposure levels. Additionally, none of the strains tested showed considerable photoreactivation or dark repair capability, implying that the induced DNA lesions were largely irreversible under our experimental conditions. This study shows the efficacy of UV-C LEDs for water disinfection across a range of wavelengths, particularly at 265 nm, highlighting the important contribution of DNA damage to bacterial inactivation, and emphasizing their applicability for the water industry.

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Data availability

Data is provided within the manuscript or supplementary information files.

References

  1. Drinking-water. World Health Organization. (2023). Available at: https://www.who.int/news-room/fact-sheets/detail/drinking-water (Accessed: 10 February 2026).

  2. Shayo, G. M., Elimbinzi, E., Shao, G. N. & Fabian, C. Severity of waterborne diseases in developing countries and the effectiveness of ceramic filters for improving water quality. Bull. Natl. Res. Centre. 47 (1), 47–113 (2023). (2023).

    Google Scholar 

  3. Bereiter, R., Vescoli, D. & Antonio Liebminger, L. Disinfection in water and used water purification. In Handbook of Water and Used Water Purification 1–32 (2021).

  4. Chatterley, C. & Linden, K. Demonstration and evaluation of germicidal UV-LEDs for point-of-use water disinfection. J. Water Health. 8, 479–486 (2010).

    Google Scholar 

  5. Song, K., Mohseni, M. & Taghipour, F. Application of ultraviolet light-emitting diodes (UV-LEDs) for water disinfection: A review. Water Res. 94, 341–349 (2016).

    Google Scholar 

  6. Beck, S. E. et al. Evaluating UV-C LED disinfection performance and investigating potential dual-wavelength synergy. Water Res. 109, 207–216 (2017).

    Google Scholar 

  7. Beck, S. E., Wright, H. B., Hargy, T. M., Larason, T. C. & Linden, K. G. Action spectra for validation of pathogen disinfection in medium-pressure ultraviolet (UV) systems. Water Res. 70, 27–37 (2015).

    Google Scholar 

  8. Itani, N. & el Fadel, M. Microbial inactivation kinetics of UV LEDs and effect of operating conditions: A methodological critical analysis. Sci. Total Environ. 885, 163727 (2023).

    Google Scholar 

  9. Martín-Sómer, M., Pablos, C., Adán, C., van Grieken, R. & Marugán, J. A review on LED technology in water photodisinfection. Sci. Total Environ. 885, 163963 (2023).

    Google Scholar 

  10. MacIsaac, S. A. et al. Improved disinfection performance for 280 nm LEDs over 254 nm low-pressure UV lamps in community wastewater. Scientific Reports 2023 13:1 13, 7576- (2023).

  11. MacIsaac, S. A. et al. UV LED wastewater disinfection: The future is upon us. Water Res. X 24, 100236 (2024).

  12. Minamata Convention on Mercury. Minamata Convention on Mercury: text and annexes. UN Environment Programme. UNEP/MC/2024/2. Pp 90. (2024). https://minamataconvention.org/en/resources/minamata-convention-mercury-text-and-annexes

  13. Li, T., Zhang, Y., Gan, J., Yu, X. & Wang, L. Superiority of UV222 radiation by in situ aquatic electrode KrCl excimer in disinfecting waterborne pathogens: Mechanism and efficacy. J Hazard. Mater 452, (2023).

  14. Ma, B. et al. UV inactivation of common pathogens and surrogates under 222 nm irradiation from KrCl* excimer lamps. Photochem. Photobiol. 99, 975–982 (2023).

    Google Scholar 

  15. Würtele, M. A. et al. Application of GaN-based ultraviolet-C light emitting diodes – UV LEDs – for water disinfection. Water Res. 45, 1481–1489 (2011).

    Google Scholar 

  16. Oliveira, B. R., Barreto Crespo, M. T. & Pereira, V. J. Small but powerful: Light-emitting diodes for inactivation of Aspergillus species in real water matrices. Water Res. 168, 115108 (2020).

    Google Scholar 

  17. Rauch, K. D. et al. A critical review of ultra-violet light emitting diodes as a one water disinfection technology. Water Res. X 25, 100271 (2024).

    Google Scholar 

  18. Sholtes, K. & Linden, K. G. Pulsed and continuous light UV LED: Microbial inactivation, electrical, and time efficiency. Water Res. 165, 114965 (2019).

  19. Huo, H. et al. Simultaneously monitoring UVC-induced DNA damage and photoenzymatic repair of cyclobutane pyrimidine dimers by electrochemical impedance spectroscopy. Talanta 239, 123081 (2022).

    Google Scholar 

  20. Nyangaresi, P. O. et al. Effects of single and combined UV-LEDs on inactivation and subsequent reactivation of E. coli in water disinfection. Water Res. 147, 331–341 (2018).

    Google Scholar 

  21. Swoboda, J. G., Campbell, J., Meredith, T. C. & Walker, S. Wall teichoic acid function, biosynthesis, and inhibition. Chembiochem 11, 35–45 (2010).

    Google Scholar 

  22. Miller, S. I. & Salama, N. R. The gram-negative bacterial periplasm: Size matters. PLoS Biol. 16, e2004935 (2018).

    Google Scholar 

  23. Silhavy, T. J. Classic spotlight: Gram-negative bacteria have two membranes. J. Bacteriol. 198, 201 (2016).

    Google Scholar 

  24. Süß, J., Volz, S., Obst, U. & Schwartz, T. Application of a molecular biology concept for the detection of DNA damage and repair during UV disinfection. Water Res. 43, 3705–3716 (2009).

    Google Scholar 

  25. McKinney, C. W. & Pruden, A. Ultraviolet disinfection of antibiotic resistant bacteria and their antibiotic resistance genes in water and wastewater. Environ Sci Technol 46, 13393–13400 (2012).

    Google Scholar 

  26. Chen, X. et al. Comparison of inactivation characteristics between Gram-positive and Gram-negative bacteria in water by synergistic UV and chlorine disinfection. Environmental Pollution 333, (2023).

  27. Chen, J., Loeb, S. & Kim, J. H. LED revolution: Fundamentals and prospects for UV disinfection applications. Environ. Sci. (Camb) 3, 188–202 (2017).

    Google Scholar 

  28. Li, X. et al. Evaluation survey of microbial disinfection methods in UV-LED water treatment systems. Sci. Total Environ. 659, 1415–1427 (2019).

    Google Scholar 

  29. Oliveira, B. R., Marques, A. P., Asif, M., Maria, M. T. & Pereira, V. J. Light-emitting diodes effect on Aspergillus species in filtered surface water: DNA damage, proteome response and potential reactivation. Environ. Pollut. 287, 117553 (2021).

    Google Scholar 

  30. Ma, D. & Hull, N. M. Impact of wavelength, exposure sequence, and organic matter on UV disinfection and DNA repair. PLoS Water 4, e0000306 (2025).

    Google Scholar 

  31. Ishida, K. et al. Efficacy of ultraviolet-light emitting diodes in bacterial inactivation and DNA damage via sensitivity evaluation using multiple wavelengths and bacterial strains. Archives of Microbiology 2025 207:6 207, 130- (2025).

  32. Hull, N. M., Herold, W. H. & Linden, K. G. UV LED water disinfection: Validation and small system demonstration study. AWWA Water Sci. 1, e1148 (2019).

    Google Scholar 

  33. Li, G. Q., Wang, W. L., Huo, Z. Y., Lu, Y. & Hu, H. Y. Comparison of UV-LED and low pressure UV for water disinfection: Photoreactivation and dark repair of Escherichia coli. Water Res 126, 134–143 (2017).

    Google Scholar 

  34. Shen, L. et al. Efficacy of UVC-LED in water disinfection on Bacillus species with consideration of antibiotic resistance issue. J Hazard. Mater 386, (2020).

  35. Pousty, D., Hofmann, R., Gerchman, Y. & Mamane, H. Wavelength-dependent time–dose reciprocity and stress mechanism for UV-LED disinfection of Escherichia coli. J Photochem Photobiol B 217, 112129 (2021).

    Google Scholar 

  36. Hull, N. M. & Linden, K. G. Synergy of MS2 disinfection by sequential exposure to tailored UV wavelengths. Water Res 143, 292–300 (2018).

    Google Scholar 

  37. Rattanakul, S. & Oguma, K. Inactivation kinetics and efficiencies of UV-LEDs against Pseudomonas aeruginosa, Legionella pneumophila, and surrogate microorganisms. Water Res 130, 31–37 (2018).

    Google Scholar 

  38. Jarvis, P., Autin, O., Goslan, E. H. & Hassard, F. Application of Ultraviolet Light-Emitting Diodes (UV-LED) to Full-Scale Drinking-Water Disinfection. Water 2019. 11, Page 1894 (11), 1894 (2019).

    Google Scholar 

  39. Mohaghegh Montazeri, M., Hejazi, S. A. & Taghipour, F. Ultraviolet light-emitting diode (UV-LED) water disinfection photoreactors: A review. J Environ Manage 386, 125678 (2025).

    Google Scholar 

  40. Basha, S. et al. Ultraviolet light-emitting diode technologies in water disinfection. Water Research X 29, 100454 (2025).

    Google Scholar 

  41. Oguma, K., Kanazawa, K., Kasuga, I. & Takizawa, S. Effects of UV irradiation by light emitting diodes on heterotrophic bacteria in tap water. Photochem. Photobiol 94, 570–576 (2018).

    Google Scholar 

  42. Oguma, K., Rattanakul, S. & Masaike, M. Inactivation of health-related microorganisms in water using UV light-emitting diodes. Water Supply. 19, 1507–1514 (2019).

    Google Scholar 

  43. Gabriel, A. A. & Musni, A. C. Prior physicochemical stress exposures and subsequent UV-C resistance of E. coli O157:H7 in coconut liquid endosperm. Food and Bioproducts Processing 117, 250–257 (2019).

    Google Scholar 

  44. Wang, Q., Buchanan, R. L. & Tikekar, R. Evaluation of adaptive response in E. coli O157:H7 to UV light and gallic acid based antimicrobial treatments. Food Control 106, 106723 (2019).

    Google Scholar 

  45. Gabriel, A. A. Previous physicochemical stress exposures influence subsequent resistance of Escherichia coli O157: H7, Salmonella enterica, and Listeria monocytogenes to ultraviolet-C in coconut liquid endosperm beverage. Int. J. Food Microbiol. 201, 7–16 (2015).

    Google Scholar 

  46. Gabriel, A. A., Estilo, E. E. C., Isnit, N. C. C. & Membrebe, B. N. Q. Suboptimal growth conditions induce heterologous ultraviolet-C adaptation in Salmonella enterica in orange juice. Food Control 62, 110–116 (2016).

    Google Scholar 

  47. Pereira, V. J., Ricardo, J., Galinha, R., Benoliel, M. J. & Barreto Crespo, M. T. Occurrence and low pressure ultraviolet inactivation of yeasts in real water sources. Photochem. Photobiol. Sci. 12, 626–630 (2013).

    Google Scholar 

  48. Fernandes, É. K. K., Rangel, D. E. N., Braga, G. U. L. & Roberts, D. W. Tolerance of entomopathogenic fungi to ultraviolet radiation: A review on screening of strains and their formulation. Curr. Genet. 61, 427–440 (2015).

    Google Scholar 

  49. Oguadinma, I. C., Mishra, A. & Kumar, G. D. Sunlight parameters influence the survival and decline of Salmonella and Escherichia coli in water. J. Food Prot. 85, 1614–1624 (2022).

    Google Scholar 

  50. Mamane-Gravetz, H. & Linden, K. G. UV disinfection of indigenous aerobic spores: Implications for UV reactor validation in unfiltered waters. Water Res. 38, 2898–2906 (2004).

    Google Scholar 

  51. Hijnen, W. A. M., Beerendonk, E. F. & Medema, G. J. Inactivation credit of UV radiation for viruses, bacteria and protozoan (oo)cysts in water: A review. Water Res. 40, 3–22 (2006).

    Google Scholar 

  52. Gayán, E., Monfort, S., Álvarez, I. & Condón, S. UV-C inactivation of Escherichia coli at different temperatures. Innov. Food Sci. Emerg. Technol. 12, 531–541 (2011).

    Google Scholar 

  53. Ichikawa, S., Okazaki, M., Okamura, M., Nishimura, N. & Miyake, H. Rare UV-resistant cells in clonal populations of Escherichia coli. J. Photochem. Photobiol. B Biol. 231, 112448 (2022).

    Google Scholar 

  54. Zimmer, J. L. & Slawson, R. M. Potential repair of Escherichia coli DNA following exposure to UV radiation from both medium- and low-pressure UV sources used in drinking water treatment. Appl. Environ. Microbiol. 68, 3293 (2002).

    Google Scholar 

  55. Bohrerova, Z. & Linden, K. G. Standardizing photoreactivation: Comparison of DNA photorepair rate in Escherichia coli using four different fluorescent lamps. Water Res. 41, 2832–2838 (2007).

    Google Scholar 

  56. Maghsoodi, M., Lowry, G. L., Smith, I. M. & Snow, S. D. Evaluation of parameters governing dark and photo-repair in UVC-irradiated Escherichia coli. Environ. Sci. Water Res. Technol. 8, 407–418 (2022).

    Google Scholar 

  57. Schindelin, J. et al. Fiji: an open-source platform for biological-image analysis. Nature Methods 2012 9:7 9, 676–682 (2012).

  58. McDonald, D., Ma, D. & Hull, N. M. 222 nm causes greater protein damage and repair inhibition of E. coli than 254 nm for water disinfection. PLoS Water 3, e0000238 (2024).

    Google Scholar 

  59. Vitzilaiou, E., Kuria, A. M., Siegumfeldt, H., Rasmussen, M. A. & Knøchel, S. The impact of bacterial cell aggregation on UV inactivation kinetics. Water Res 204, (2021).

  60. Jaiaue, P. et al. Mathematical modeling for evaluating inherent parameters affecting UVC decontamination of indicator bacteria. Appl. Environ. Microbiol. 88, e02148-21 (2022).

    Google Scholar 

  61. Sandoz, K. M. et al. β-Barrel proteins tether the outer membrane in many Gram-negative bacteria. Nat. Microbiol. 6, 19–26 (2021).

    Google Scholar 

  62. Mamou, G. et al. Peptidoglycan maturation controls outer membrane protein assembly. Nature 2022 606:7916 606, 953–959 (2022).

  63. Cheigh, C. I., Park, M. H., Chung, M. S., Shin, J. K. & Park, Y. S. Comparison of intense pulsed light- and ultraviolet (UVC)-induced cell damage in Listeria monocytogenes and Escherichia coli O157:H7. Food Control 25, 654–659 (2012).

    Google Scholar 

  64. Liu, Z. et al. Evaluation of disinfection performance of a multiple wavelength EBE-UV light source and comparison with UV-LEDs. J. Environ. Chem. Eng. 11, 110063 (2023).

    Google Scholar 

  65. Markovitsi, D., Gustavsson, T. & Banyasz, A. Absorption of UV radiation by DNA: Spatial and temporal features. Mutat. Research/Reviews Mutat. Res. 704, 21–28 (2010).

    Google Scholar 

  66. Lanzarini-Lopes, M. et al. Nanoparticle and transparent polymer coatings enable UV-C side-emission optical fibers for inactivation of Escherichia coli in water. Environ. Sci. Technol. 53, 10880–10887 (2019).

    Google Scholar 

  67. Pendyala, B., Vashisht, P., Sharma, A., Patras, A. & Balamurugan, S. Wavelength-specific UV-C inactivation kinetics of foodborne pathogens in stirred liquid suspensions and droplets on contact surfaces. LWT 196, 115846 (2024).

    Google Scholar 

  68. Bowker, C., Sain, A., Shatalov, M. & Ducoste, J. Microbial UV fluence-response assessment using a novel UV-LED collimated beam system. Water Res. 45, 2011–2019 (2011).

    Google Scholar 

  69. Kamel, A., Fuentes, M., Palacios, A. M., Rodrigo, M. J. & Vivar, M. Deactivating environmental strains of Escherichia coli, Enterococcus faecalis and Clostridium perfringens from a real wastewater effluent using UV-LEDs. Heliyon 8, e12628 (2022).

    Google Scholar 

  70. Kamel, A., Palacios, A., Fuentes, M. & Vivar, M. Analysing the Reciprocity Law for UV-LEDs in Water Disinfection of Escherichia coli, Enterococcus faecalis, and Clostridium perfringens. Water (Basel) 15, (2023).

  71. Silva, I. et al. Fate of cefotaxime-resistant Enterobacteriaceae and ESBL-producers over a full-scale wastewater treatment process with UV disinfection. Sci. Total Environ. 639, 1028–1037 (2018).

    Google Scholar 

  72. Martins, M. E. Study of light-emitting diodes for water disinfection (Master’s thesis). Faculty of Science and Technology, University of Algarve (2024).

  73. Bolton, J. R. & Linden, K. G. Standardization of methods for fluence (UV dose) determination in bench-scale UV experiments. J. Environ. Eng. 129, 209–215 (2003).

    Google Scholar 

  74. U.S. Environmental Protection Agency. Ultraviolet Disinfection Guidance Manual for the Final Long Term 2 Enhanced Surface Water Treatment Rule. EPA 815-R-06-007 (U.S. Environmental Protection Agency, 2006).

  75. Sinha, R. P. & Häder, D. P. UV-induced DNA damage and repair: A review. Photochem. Photobiol. Sci. 1, 225–236 (2002).

    Google Scholar 

  76. Oguma, K. et al. Determination of pyrimidine dimers in Escherichia coli and Cryptosporidium parvum during UV light inactivation, photoreactivation, and dark repair. Appl. Environ. Microbiol. 67, 4630 (2001).

    Google Scholar 

  77. Oguma, K., Katayama, H. & Ohgaki, S. Photoreactivation of Escherichia coli after low- or medium-pressure UV disinfection determined by an endonuclease sensitive site assay. Appl. Environ. Microbiol. 68, 6029 (2002).

    Google Scholar 

  78. Xiao, Y., Chu, X. N., He, M., Liu, X. C. & Hu, J. Y. Impact of UVA pre-radiation on UVC disinfection performance: Inactivation, repair and mechanism study. Water Res. 141, 279–288 (2018).

    Google Scholar 

  79. Song, K., Taghipour, F. & Mohseni, M. Microorganisms inactivation by wavelength combinations of ultraviolet light-emitting diodes (UV-LEDs). Sci. Total Environ. 665, 1103–1110 (2019).

    Google Scholar 

  80. Xiong, P. & Hu, J. Inactivation/reactivation of antibiotic-resistant bacteria by a novel UVA/LED/TiO2 system. Water Res. 47, 4547–4555 (2013).

    Google Scholar 

  81. Balaban, N. Q. et al. Definitions and guidelines for research on antibiotic persistence. Nature Reviews Microbiology 2019 17:7 17, 441–448 (2019).

  82. García-Contreras, R. et al. Quorum sensing enhancement of the stress response promotes resistance to quorum quenching and prevents social cheating. ISME J. 9, 115–125 (2015).

    Google Scholar 

  83. Banerji, R., Karkee, A., Kanojiya, P., Patil, A. & Saroj, S. D. Bacterial communication in the regulation of stress response in Listeria monocytogenes. LWT 154, 112703 (2022).

    Google Scholar 

  84. Zhang, Y. et al. UV-Induced VBNC state formation and resuscitation in E. coli: ATP-based metabolic activation and biofilm-mediated recovery. Water Res. 287, 124380 (2025).

    Google Scholar 

  85. Pan, H. & Ren, Q. Wake Up! Resuscitation of Viable but Nonculturable Bacteria: Mechanism and Potential Application. Foods 2023. 12, Page 82 (12), 82 (2022).

    Google Scholar 

  86. Kirsch, J. et al. A UV-C LED-based unit for continuous decontamination of the sheath fluid in a flow-cytometric cell sorter. Eng. Life Sci. 22, 550–553 (2022).

    Google Scholar 

  87. Kim, D. K., Kim, S. J. & Kang, D. H. Bactericidal effect of 266 to 279 nm wavelength UVC-LEDs for inactivation of Gram positive and Gram negative foodborne pathogenic bacteria and yeasts. Food Res. Int. 97, 280–287 (2017).

    Google Scholar 

  88. Chen, Y. C., Kalawong, R., Toyofuku, M. & Eberl, L. The role of peptidoglycan hydrolases in the formation and toxicity of Pseudomonas aeruginosa membrane vesicles. microLife 3, (2022).

  89. Gamalier, J. P., Silva, T. P., Zarantonello, V., Dias, F. F. & Melo, R. C. N. Increased production of outer membrane vesicles by cultured freshwater bacteria in response to ultraviolet radiation. Microbiol. Res. 194, 38–46 (2017).

    Google Scholar 

  90. Kollu, K. & Örmeci, B. UV-induced self-aggregation of E. coli after low and medium pressure ultraviolet irradiation. J. Photochem. Photobiol B. 148, 310–321 (2015).

    Google Scholar 

  91. Cheng, Y. et al. Inactivation of Listeria and E. coli by Deep-UV LED: effect of substrate conditions on inactivation kinetics. Scientific Reports 2020 10:1 10, 3411- (2020).

  92. Cushnie, T. P. T., O’Driscoll, N. H. & Lamb, A. J. Morphological and ultrastructural changes in bacterial cells as an indicator of antibacterial mechanism of action. Cellular and Molecular Life Sciences 2016 73:23 73, 4471–4492 (2016).

  93. Vauclare, P. et al. Stress-induced nucleoid remodeling in Deinococcus radiodurans is associated with major changes in heat unstable (HU) protein dynamics. Nucleic Acids Res. 52, 6406–6423 (2024).

    Google Scholar 

  94. Shibai, A. et al. Mutation accumulation under UV radiation in Escherichia coli. Sci. Rep. 7 (1), 7–14531 (2017). (2017).

    Google Scholar 

  95. Justice, S. S., Hunstad, D. A., Seed, P. C. & Hultgren, S. J. Filamentation by Escherichia coli subverts innate defenses during urinary tract infection. Proceedings of the National Academy of Sciences 103, 19884–19889 (2006).

  96. Ansari, S. et al. A newly identified prophage-encoded gene, ymfM, causes SOS-inducible filamentation in Escherichia coli. J Bacteriol 203, (2021).

  97. Cayron, J., Dedieu-Berne, A. & Lesterlin, C. Bacterial filaments recover by successive and accelerated asymmetric divisions that allow rapid post-stress cell proliferation. Mol. Microbiol. 119, 237–251 (2023).

    Google Scholar 

  98. Loiko, N. et al. DNA-Binding Protein Dps Protects Escherichia coli Cells against Multiple Stresses during Desiccation. Biology (Basel) 12, (2023).

  99. Stringer, C., Wang, T., Michaelos, M. & Pachitariu, M. Cellpose: a generalist algorithm for cellular segmentation. Nature Methods 2020 18:1 18, 100–106 (2020).

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Funding

This work was funded by Fundação para a Ciência e a Tecnologia/Ministério da Ciência, Tecnologia e Ensino Superior (FCT/MCTES, Portugal) through the projects PTDC/EAM-AMB/1561/2021, 2022.12621.BD (DOI identifier - https://doi.org/10.54499/2022.12621.BD) as well as the Stimulus of Scientific Employment Grant CEECIND/02919/2018.

This work was also supported by the Research Units Green-it Bioresources for Sustainability (UID/04551/2025, DOI: 10.54499/UID/04551/2025; UID/PRR/04551/2025, DOI: 10.54499/UID/PRR/04551/2025) and UID/04462: iNOVA4Health – Programme in Translational Medicine, financially supported by Fundação para a Ciência e Tecnologia/Ministério da Educação, Ciência e Inovação, as well as the Associate Laboratory LS4FUTURE (LA/P/0087/2020).

This work was partially supported by PPBI - Portuguese Platform of BioImaging (PPBI-POCI-01-0145-FEDER-022122) co-funded by national funds from OE - “Orçamento de Estado” and by European funds from FEDER - “Fundo Europeu de Desenvolvimento Regional”.

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  1. Ana Paula Marques

    Present address: INIAV, IP - Instituto Nacional de Investigação Agrária e Veterinária - Pólo de Inovação Dois Portos, Quinta da Almoinha, 2565-191, Dois Portos, Portugal

Authors and Affiliations

  1. iBET - Instituto de Biologia Experimental e Tecnológica, Apartado 12, 2781-901, Oeiras, Portugal

    João Sério, Carolina Santos, Maria Eduarda Martins, Ana Paula Marques, Maria Teresa Barreto Crespo & Vanessa Jorge Pereira

  2. Instituto de Tecnologia Química e Biológica António Xavier, Universidade Nova de Lisboa, Av. da República, Oeiras, 2780-157, Portugal

    João Sério, Carolina Santos, Carolina Feliciano, Mónica Serrano, Adriano O. Henriques, Maria Teresa Barreto Crespo & Vanessa Jorge Pereira

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Contributions

Vanessa Pereira: Conceptualization; João Sério, Carolina Santos, Maria Eduarda Martins, Ana Paula Marques and Carolina Feliciano: Research and investigation; Vanessa Pereira, Ana Paula Marques, Maria Teresa Barreto Crespo, Mónica Serrano and Adriano Henriques: Methodology and supervision; João Sério: Writing – original draft; All authors: Writing – review & editing.

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Correspondence to Vanessa Jorge Pereira.

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Sério, J., Santos, C., Martins, M.E. et al. UV-C LED wavelength effects on inactivation kinetics, DNA damage and membrane integrity in drinking water indicator bacteria. Sci Rep (2026). https://doi.org/10.1038/s41598-026-44556-8

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  • Received: 18 September 2025

  • Accepted: 12 March 2026

  • Published: 03 April 2026

  • DOI: https://doi.org/10.1038/s41598-026-44556-8

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Keywords

  • Water treatment
  • Disinfection
  • Ultraviolet light emitting diodes
  • Wavelengths
  • Water quality indicators
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Water pollution and advanced treatment processes

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