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DNA damage Kills Bacterial Spores and Cells Exposed to 222 nm UV Radiation

Taylor, Willie und Camilleri, Emily und Craft, D. Levi und Korza, George und Rocha Granados, Maria und Peterson, Jaliyah und Szczpaniak, Renata und Weller, Sandra K. und Moeller, Ralf und Douki, Thierry und Mok, Wendy W.K. und Setlow, Peter (2020) DNA damage Kills Bacterial Spores and Cells Exposed to 222 nm UV Radiation. Applied and Environmental Microbiology, 86 (8), e03039-19. American Society for Microbiology. doi: 10.1128/AEM.03039-19. ISSN 0099-2240.

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Offizielle URL: http://dx.doi.org/10.1128/AEM.03039-19

Kurzfassung

This study examined the microbicidal activity of 222 nm UV radiation (UV₂₂₂), which is potentially a safer alternative to the 254 nm UV radiation (UV₂₅₄) that is often used for surface decontamination. Spores and/or growing and stationary phase cells of Bacillus cereus, Bacillus subtilis, Bacillus thuringiensis, Staphylococcus aureus and Clostridioides difficile, and a Herpes virus were all killed or inactivated by UV₂₂₂, and at lower fluences than with UV₂₅₄. B. subtilis spores and cells lacking the major DNA repair protein RecA were more sensitive to UV₂₂₂, as were spores lacking their DNA protective proteins, the α/β-type small, acid-soluble spore proteins. The spore cores' large amount of Ca²⁺-dipicolinic acid (∼25% of core dry wt) also protected B. subtilis and C. difficile spores against UV₂₂₂, while spores' proteinaceous coat may have given some slight protection against UV₂₂₂. Survivors of B. subtilis spores treated with UV₂₂₂ acquired a large number of mutations, and this radiation generated known mutagenic photoproducts in spore and cell DNA - primarily cyclobutane-type pyrimidine dimers in growing cells, and an α-thyminyl-thymine adduct termed the spore photoproduct (SP) in spores. Notably, loss of a key SP repair protein markedly decreased spore UV₂₂₂ resistance. UV₂₂₂-treated B. subtilis spores germinated relatively normally, and generation of colonies from these germinated spores was not salt-sensitive. The latter two findings suggest that UV₂₂₂ does not kill spores by general protein damage, and thus the new results are consistent with the notion that DNA damage is responsible for killing of spores and cells by UV₂₂₂. IMPORTANCE Spores of a variety of bacteria are resistant to common decontamination agents, and many of them are major causes of food spoilage and some serious human diseases, including anthrax caused by spores of Bacillus anthracis. Consequently, there is an ongoing need for efficient methods for spore eradication, in particular methods that have minimal deleterious effects on people or the environment. Ultraviolet radiation (UV) at 254 nanometers (UV₂₅₄) is sporicidal and commonly used for surface decontamination, but can cause deleterious effects in humans. Recent work, however, suggests that 222 nm UV (UV₂₂₂) may be less harmful to people than UV₂₅₄, yet still kill bacteria and at lower fluences than UV₂₅₄. The current work has identified the damage by UV₂₂₂ that leads to killing of growing cells and spores of some bacteria many of which are human pathogens, and UV₂₂₂ also inactivates a Herpes virus.

elib-URL des Eintrags:https://elib.dlr.de/134218/
Dokumentart:Zeitschriftenbeitrag
Titel:DNA damage Kills Bacterial Spores and Cells Exposed to 222 nm UV Radiation
Autoren:
AutorenInstitution oder E-Mail-AdresseAutoren-ORCID-iDORCID Put Code
Taylor, WillieDepartment of Molecular Biology and Biophysics, UConn Health, Farmington, CT USA 06030-3305NICHT SPEZIFIZIERTNICHT SPEZIFIZIERT
Camilleri, EmilyDepartment of Molecular Biology and Biophysics, UConn Health, Farmington, CT USA 06030-3305NICHT SPEZIFIZIERTNICHT SPEZIFIZIERT
Craft, D. LeviDepartment of Molecular Biology and Biophysics, UConn Health, Farmington, CT USA 06030-3305NICHT SPEZIFIZIERTNICHT SPEZIFIZIERT
Korza, GeorgeDepartment of Molecular Biology and Biophysics, UConn Health, Farmington, CT USA 06030-3305NICHT SPEZIFIZIERTNICHT SPEZIFIZIERT
Rocha Granados, MariaDepartment of Molecular Biology and Biophysics, UConn Health, Farmington, CT USA 06030-3305NICHT SPEZIFIZIERTNICHT SPEZIFIZIERT
Peterson, JaliyahDepartment of Molecular Biology and Biophysics, UConn Health, Farmington, CT USA 06030-3305NICHT SPEZIFIZIERTNICHT SPEZIFIZIERT
Szczpaniak, RenataDepartment of Molecular Biology and Biophysics, UConn Health, Farmington, CT USA 06030-3305NICHT SPEZIFIZIERTNICHT SPEZIFIZIERT
Weller, Sandra K.Department of Molecular Biology and Biophysics, UConn Health, Farmington, CT USA 06030-3305NICHT SPEZIFIZIERTNICHT SPEZIFIZIERT
Moeller, RalfRadiation Biology Department, Institute of Aerospace Medicine, German Aerospace Center (DLR), Cologne, Germany; ralf.moeller (at) dlr.dehttps://orcid.org/0000-0002-2371-0676NICHT SPEZIFIZIERT
Douki, ThierryUniversite Grenoble Alpes, CEA, CNRS, INAC-SYMMBEST, Grenoble, FranceNICHT SPEZIFIZIERTNICHT SPEZIFIZIERT
Mok, Wendy W.K.Department of Molecular Biology and Biophysics, UConn Health, Farmington, CT USA 06030-3305NICHT SPEZIFIZIERTNICHT SPEZIFIZIERT
Setlow, PeterDepartment of Molecular Biology and Biophysics, UConn Health, Farmington, CT USA 06030-3305; setlow (at) nso2.uchc.eduNICHT SPEZIFIZIERTNICHT SPEZIFIZIERT
Datum:7 Februar 2020
Erschienen in:Applied and Environmental Microbiology
Referierte Publikation:Ja
Open Access:Nein
Gold Open Access:Nein
In SCOPUS:Ja
In ISI Web of Science:Ja
Band:86
DOI:10.1128/AEM.03039-19
Seitenbereich:e03039-19
Verlag:American Society for Microbiology
ISSN:0099-2240
Status:veröffentlicht
Stichwörter:microbicidal activity, 222 nm UV Radiation, surface decontamination
HGF - Forschungsbereich:Luftfahrt, Raumfahrt und Verkehr
HGF - Programm:Raumfahrt
HGF - Programmthema:Forschung unter Weltraumbedingungen
DLR - Schwerpunkt:Raumfahrt
DLR - Forschungsgebiet:R FR - Forschung unter Weltraumbedingungen
DLR - Teilgebiet (Projekt, Vorhaben):R - Vorhaben Strahlenbiologie (alt)
Standort: Köln-Porz
Institute & Einrichtungen:Institut für Luft- und Raumfahrtmedizin > Strahlenbiologie
Hinterlegt von: Kopp, Kerstin
Hinterlegt am:06 Mär 2020 09:08
Letzte Änderung:06 Mär 2020 09:08

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