Reactive oxygen species generated by irradiation with bandpass-filtered 222-nm Far-UVC play an important role in the germicidal mechanism to Escherichia coli.

IF 3.7 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Applied and Environmental Microbiology Pub Date : 2025-02-19 Epub Date: 2025-01-31 DOI:10.1128/aem.01886-24
Kouji Narita, Risako Fukushi, Kyosuke Yamane, Yoshihiko Okumura, Toru Koi, Krisana Asano, Akio Nakane
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Abstract

Ultraviolet (UV) C light emitted by a krypton chloride (KrCl) lamp consists of mainly less harmful 222-nm Far-UVC (unfiltered 222-mm Far-UVC) compared with conventionally used 254-nm UVC. It also contains wavelengths that are harmful to mammalian cells. By contrast, UVC from a KrCl lamp with optical filter (filtered 222-nm Far-UVC) consists of much less harmful 222-nm Far-UVC and is available for sterilization of dwelling spaces. The germicidal mechanisms of the 254-nm UVC and unfiltered 222-nm Far-UVC have been partially elucidated; however, the mechanism of action of filtered 222-nm Far-UVC remains unknown. It is known that 254 nm UVC induces cyclobutene pyrimidine dimers (CPDs), which are DNA lesions in Escherichia coli (E. coli); however, the CPDs are repaired by photoreactivation. In the present study, it was demonstrated that filtered 222-nm Far-UVC also generated CPDs, which were not repaired by photoreactivation. Therefore, a germicidal mechanism of filtered 222-nm Far-UVC may be different from a 254-nm UVC. It was reported that unfiltered 222-nm Far-UVC induced reactive oxygen species (ROS) in E. coli. In the present study, filtered 222-nm Far-UVC also induced ROS production. In accordance with increased ROS production, the levels of carbonylated proteins were increased, and morphological alteration was observed in E. coli. From these results, it was suggested that ROS generated by filtered 222-nm Far-UVC inactivated ROS scavenger enzymes and the enzyme photolyase that is involved in photoreactivation. The increased ROS levels and unrepaired CPDs impaired photoreactivation in E. coli and may be involved in the germicidal mechanism of action of the filtered 222-nm Far-UVC.IMPORTANCEThe 222 nm Far-ultraviolet (UV) C light (UVC) emitted from a krypton chloride lamp with an optical filter is currently available for the sterilization of dwelling spaces. To use the filtered 222-nm Far-UVC more effectively and safely for sterilization, it is necessary to understand its germicidal mechanism. The present study suggests that the germicidal effect of filtered 222-nm Far-UVC on E. coli may not only involve CPD but also ROS. These results could be useful in establishing more effective preventive methods in dwelling spaces for infectious diseases by UVC irradiation.

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通过带通过滤的222 nm远紫外线照射产生的活性氧在对大肠杆菌的杀菌机制中起重要作用。
与常规使用的254纳米UVC相比,氯氪(KrCl)灯发出的紫外线(UV) C主要由危害较小的222纳米远紫外线(未经过滤的222毫米远紫外线)组成。它还含有对哺乳动物细胞有害的波长。相比之下,带有光学滤光片的KrCl灯(过滤222纳米远紫外线)产生的UVC含有危害小得多的222纳米远紫外线,可用于住宅空间的消毒。254 nm UVC和未经过滤的222 nm远UVC的杀菌机理已经部分阐明;然而,222纳米远紫外线过滤后的作用机制尚不清楚。已知254 nm UVC诱导环丁烯嘧啶二聚体(CPDs),这是大肠杆菌(E. coli)的DNA损伤;然而,cpd是通过光再激活修复的。在本研究中,我们发现过滤后的222nm远紫外线也会产生CPDs,而CPDs不能通过光活化来修复。因此,222纳米远紫外线的杀菌机制可能与254纳米远紫外线不同。据报道,未经过滤的222 nm远紫外线诱导大肠杆菌的活性氧(ROS)。在本研究中,经过过滤的222nm远紫外线也能诱导ROS的产生。随着ROS产生的增加,大肠杆菌中羰基化蛋白的水平增加,并观察到形态学改变。从这些结果可以看出,通过过滤222nm远紫外线产生的活性氧灭活了ROS清除酶和参与光再激活的酶光解酶。活性氧水平升高和未修复的CPDs损伤了大肠杆菌的光活化,这可能与过滤后的222nm远紫外线的杀菌机制有关。从带有光学滤光片的氯氪灯发出的222 nm远紫外(UV) C光(UVC)目前可用于住宅空间的消毒。为了更有效、安全地利用过滤后的222nm远紫外线进行杀菌,有必要了解其杀菌机理。本研究提示,222 nm远紫外线过滤后对大肠杆菌的杀菌作用可能不仅涉及CPD,还涉及活性氧。这些结果可用于建立更有效的居住空间紫外线照射传染病预防方法。
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来源期刊
Applied and Environmental Microbiology
Applied and Environmental Microbiology 生物-生物工程与应用微生物
CiteScore
7.70
自引率
2.30%
发文量
730
审稿时长
1.9 months
期刊介绍: Applied and Environmental Microbiology (AEM) publishes papers that make significant contributions to (a) applied microbiology, including biotechnology, protein engineering, bioremediation, and food microbiology, (b) microbial ecology, including environmental, organismic, and genomic microbiology, and (c) interdisciplinary microbiology, including invertebrate microbiology, plant microbiology, aquatic microbiology, and geomicrobiology.
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