Role of the Pseudomonas quinolone signal (PQS) in sensitising Pseudomonas aeruginosa to UVA radiation

•PQS sensitises Pseudomonas aeruginosa exposed to UVA radiation.•Exposure of PQS to UVA radiation generates singlet oxygen and superoxide anion.•PQS could act as endogenous photosensitizer in Pseudomonas aeruginosa cells. One of the main stress factors that bacteria face in the environment is solar...

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Veröffentlicht in:Journal of photochemistry and photobiology. B, Biology Biology, 2015-01, Vol.142, p.129-140
Hauptverfasser: Pezzoni, Magdalena, Meichtry, Martín, Pizarro, Ramón A., Costa, Cristina S.
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Sprache:eng
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Zusammenfassung:•PQS sensitises Pseudomonas aeruginosa exposed to UVA radiation.•Exposure of PQS to UVA radiation generates singlet oxygen and superoxide anion.•PQS could act as endogenous photosensitizer in Pseudomonas aeruginosa cells. One of the main stress factors that bacteria face in the environment is solar ultraviolet-A (UVA) radiation, which leads to lethal effects through oxidative damage. The aim of this work was to investigate the role of 2-heptyl-3-hydroxi-4-quinolone (the Pseudomonas quinolone signal or PQS) in the response of Pseudomonas aeruginosa to UVA radiation. PQS is an intercellular quorum sensing signal associated to membrane vesicles which, among other functions, regulates genes related to iron acquisition, forms stable complexes with iron and participates in oxidative phenomena. UVA exposure of the wild-type PAO1 strain and a pqsA mutant unable to produce PQS revealed a sensitising role for this signal. Research into the mechanism involved in this phenomenon revealed that catalase, an essential factor in the UVA defence, is not related to PQS-mediated UVA sensitivity. Absorption of UVA by PQS produced its own photo-degradation, oxidation of the probe 2′,7′- dichlorodihydrofluorescein and generation of singlet oxygen and superoxide anion, suggesting that this signal could be acting as an endogenous photosensitiser. The results presented in this study could explain the high sensitivity to UVA of P. aeruginosa when compared to enteric bacteria.
ISSN:1011-1344
1873-2682
DOI:10.1016/j.jphotobiol.2014.11.014