scholarly journals Antimicrobial Blue Light Inactivation ofNeisseria gonorrhoeae: Roles of Wavelength, Endogenous Photosensitizer, Oxygen, and Reactive Oxygen Species

2019 ◽  
Vol 51 (9) ◽  
pp. 815-823 ◽  
Author(s):  
Ying Wang ◽  
Raquel Ferrer‐Espada ◽  
Yan Baglo ◽  
Ying Gu ◽  
Tianhong Dai
2006 ◽  
Vol 77A (3) ◽  
pp. 470-477 ◽  
Author(s):  
Y. Omata ◽  
J.B. Lewis ◽  
S. Rotenberg ◽  
P.E. Lockwood ◽  
R.L.W. Messer ◽  
...  

2005 ◽  
Vol 21 (7) ◽  
pp. 683-688 ◽  
Author(s):  
Daniel B. Lockwood ◽  
John C. Wataha ◽  
Jill B. Lewis ◽  
Wan Y. Tseng ◽  
Regina L.W. Messer ◽  
...  

2016 ◽  
Vol 82 (13) ◽  
pp. 4017-4027 ◽  
Author(s):  
Beth O'Donoghue ◽  
Kerrie NicAogáin ◽  
Claire Bennett ◽  
Alan Conneely ◽  
Teresa Tiensuu ◽  
...  

ABSTRACTListeria monocytogenessenses blue light via the flavin mononucleotide-containing sensory protein Lmo0799, leading to activation of the general stress response sigma factor SigB (σB). In this study, we investigated the physiological response of this foodborne pathogen to blue light. We show that blue light (460 to 470 nm) doses of 1.5 to 2 mW cm−2cause inhibition of growth on agar-based and liquid culture media. The inhibitory effects are dependent on cell density, with reduced effects evident when high cell numbers are present. The addition of 20 mM dimethylthiourea, a scavenger of reactive oxygen species, or catalase to the medium reverses the inhibitory effects of blue light, suggesting that growth inhibition is mediated by the formation of reactive oxygen species. A mutant strain lacking σB(ΔsigB) was found to be less inhibited by blue light than the wild type, likely indicating the energetic cost of deploying the general stress response. When a lethal dose of light (8 mW cm−2) was applied to cells, the ΔsigBmutant displayed a marked increase in sensitivity to light compared to the wild type. To investigate the role of the blue-light sensor Lmo0799, mutants were constructed that either had a deletion of the gene (Δlmo0799) or alteration in a conserved cysteine residue at position 56, which is predicted to play a pivotal role in the photocycle of the protein (lmo0799C56A). Both mutants displayed phenotypes similar to the ΔsigBmutant in the presence of blue light, providing genetic evidence that residue 56 is critical for light sensing inL. monocytogenes. Taken together, these results demonstrate thatL. monocytogenesis inhibited by blue light in a manner that depends on reactive oxygen species, and they demonstrate clear light-dependent phenotypes associated with σBand the blue-light sensor Lmo0799.IMPORTANCEListeria monocytogenesis a bacterial foodborne pathogen that can cause life-threatening infections in humans. It is known to be able to sense and respond to visible light. In this study, we examine the effects of blue light on the growth and survival of this pathogen. We show that growth can be inhibited at comparatively low doses of blue light, and that at higher doses,L. monocytogenescells are killed. We present evidence suggesting that blue light inhibits this organism by causing the production of reactive oxygen species, such as hydrogen peroxide. We help clarify the mechanism of light sensing by constructing a “blind” version of the blue-light sensor protein. Finally, we show that activation of the general stress response by light has a negative effect on growth, probably because cellular resources are diverted into protective mechanisms rather than growth.


2021 ◽  
Vol 22 (4) ◽  
pp. 2015
Author(s):  
Ying Li ◽  
Rujun Jin ◽  
Lan Li ◽  
Ji Suk Choi ◽  
Jonghwa Kim ◽  
...  

In this study, we investigated the effects of blue light exposure on nucleotide-binding oligomerization domain 2 (NOD2) expression on the mouse ocular surface and evaluated the role of NOD2 activation in light-induced cell death. Mice were divided into wild-type (WT), NOD2-knock out (KO), WT + blue light (WT + BL), and NOD2-KO + blue light (NOD2-KO + BL) groups, and the mice in the WT+BL and NOD2-KO + BL groups were exposed to blue light for 10 days. After 10 days of blue light exposure, increased reactive oxygen species and malondialdehyde were observed in the WT + BL and NOD2-KO + BL groups, and the WT + BL group showed a higher expression of NOD2 and autophagy related 16 like 1. Although both WT+BL and NOD2-KO + BL groups showed an increase in the expression of light chain 3-II, NOD2-KO + BL mice had a significantly lower p62 expression than WT + BL mice. In addition, NOD2-KO+BL mice had significantly lower corneal epithelial damage and apoptosis than WT + BL mice. In conclusion, blue light exposure can induce impaired autophagy by activation of NOD2 on the ocular surface. In addition, the reactive oxygen species (ROS)–NOD2–autophagy related 16 like 1 (ATG16L) signaling pathway may be involved in the blue-light-induced autophagy responses, resulting in corneal epithelial apoptosis.


2008 ◽  
Vol 24 (8) ◽  
pp. 1070-1076 ◽  
Author(s):  
Serge Bouillaguet ◽  
Brandi Owen ◽  
John C. Wataha ◽  
Marino A. Campo ◽  
Norbert Lange ◽  
...  

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