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紫外线发光二极管照射可通过抑制病毒 RNA 在宿主细胞中的复制和转录来使甲型流感病毒失活。

Irradiation by ultraviolet light-emitting diodes inactivates influenza a viruses by inhibiting replication and transcription of viral RNA in host cells.

机构信息

Department of Preventive Environment and Nutrition, Institute of Biomedical Sciences, Tokushima University Graduate School, Kuramoto-cho 3-18-15, Tokushima City, Tokushima 770-8503, Japan.

Department of Preventive Environment and Nutrition, Institute of Biomedical Sciences, Tokushima University Graduate School, Kuramoto-cho 3-18-15, Tokushima City, Tokushima 770-8503, Japan.

出版信息

J Photochem Photobiol B. 2018 Dec;189:193-200. doi: 10.1016/j.jphotobiol.2018.10.017. Epub 2018 Oct 29.

DOI:10.1016/j.jphotobiol.2018.10.017
PMID:30391908
Abstract

Influenza A viruses (IAVs) pose a serious global threat to humans and their livestock, especially poultry and pigs. This study aimed to investigate how to inactivate IAVs by using different ultraviolet-light-emitting diodes (UV-LEDs). We developed sterilization equipment with light-emitting diodes (LEDs) those peak wavelengths were 365 nm (UVA-LED), 310 nm (UVB-LED), and 280 nm (UVC-LED). These UV-LED irradiations decreased dose fluence-dependent plaque-forming units of IAV H1N1 subtype (A/Puerto Rico/8/1934) infected Madin-Darby canine kidney (MDCK) cells, but the inactivation efficiency of UVA-LED was significantly lower than UVB- and UVC-LED. UV-LED irradiations did not alter hemagglutination titer, but decreased accumulation of intracellular total viral RNA in infected MDCK cells was observed. Additionally, UV-LED irradiations suppressed the accumulation of intracellular mRNA (messenger RNA), vRNA (viral RNA), and cRNA (complementary RNA), as measured by strand-specific RT-PCR. These results suggest that UV-LEDs inhibit host cell replication and transcription of viral RNA. Both UVB- and UVC-LED irradiation decreased focus-forming unit (FFU) of H5N1 subtype (A/Crow/Kyoto/53/2004), a highly pathogenic avian IAV (HPAI), in infected MDCK cells, and the amount of FFU were lower than the H1N1 subtype. From these results, it appears that IAVs may have different sensitivity among the subtypes, and UVB- and UVC-LED may be suitable for HPAI virus inactivation.

摘要

甲型流感病毒(IAV)对人类及其家畜,尤其是家禽和猪,构成了严重的全球威胁。本研究旨在探讨如何使用不同的紫外线发光二极管(UV-LED)来使 IAV 失活。我们开发了带有发光二极管(LED)的消毒设备,其峰值波长分别为 365nm(UVA-LED)、310nm(UVB-LED)和 280nm(UVC-LED)。这些 UV-LED 照射使感染 Madin-Darby 犬肾(MDCK)细胞的甲型流感病毒 H1N1 亚型(A/Puerto Rico/8/1934)的剂量依赖性空斑形成单位减少,但 UVA-LED 的失活效率明显低于 UVB 和 UVC-LED。UV-LED 照射不改变血凝滴度,但观察到感染的 MDCK 细胞中细胞内总病毒 RNA 的积累减少。此外,UV-LED 照射抑制了感染的 MDCK 细胞中细胞内 mRNA(信使 RNA)、vRNA(病毒 RNA)和 cRNA(互补 RNA)的积累,这通过特异性 RT-PCR 进行测量。这些结果表明,UV-LED 抑制了宿主细胞复制和病毒 RNA 的转录。UVB 和 UVC-LED 照射均降低了感染的 MDCK 细胞中 H5N1 亚型(A/Crow/Kyoto/53/2004)的空斑形成单位(FFU),该病毒为高致病性禽流感病毒(HPAI),且 FFU 数量低于 H1N1 亚型。从这些结果来看,IAV 可能在亚型之间具有不同的敏感性,而 UVB 和 UVC-LED 可能适用于 HPAI 病毒失活。

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