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冷大气压等离子体对生物膜中耐甲氧西林细胞造成蛋白质损伤。

Cold Atmospheric-Pressure Plasma Caused Protein Damage in Methicillin-Resistant Cells in Biofilms.

作者信息

Guo Li, Yang Lu, Qi Yu, Niyazi Gulimire, Huang Lingling, Gou Lu, Wang Zifeng, Zhang Lei, Liu Dingxin, Wang Xiaohua, Chen Hailan, Kong Michael G

机构信息

State Key Laboratory of Electrical Insulation and Power Equipment, Center for Plasma Biomedicine, Xi'an Jiaotong University, Xi'an 710049, China.

School of Life Science and Technology, Xi'an Jiaotong University, Xi'an 710049, China.

出版信息

Microorganisms. 2021 May 17;9(5):1072. doi: 10.3390/microorganisms9051072.

Abstract

Biofilms formed by multidrug-resistant bacteria are a major cause of hospital-acquired infections. Cold atmospheric-pressure plasma (CAP) is attractive for sterilization, especially to disrupt biofilms formed by multidrug-resistant bacteria. However, the underlying molecular mechanism is not clear. In this study, CAP effectively reduced the living cells in the biofilms formed by methicillin-resistant , and 6 min treatment with CAP reduced the cells in biofilms by 3.5 log. The treatment with CAP caused the polymerization of SaFtsZ and SaClpP proteins in the cells of the biofilms. In vitro analysis demonstrated that recombinant SaFtsZ lost its self-assembly capability, and recombinant SaClpP lost its peptidase activity after 2 min of treatment with CAP. Mass spectrometry showed oxidative modifications of a cluster of peaks differing by 16 Da, 31 Da, 32 Da, 47 Da, 48 Da, 62 Da, and 78 Da, induced by reactive species of CAP. It is speculated that the oxidative damage to proteins in cells was induced by CAP, which contributed to the reduction of biofilms. This study elucidates the biological effect of CAP on the proteins in bacterial cells of biofilms and provides a basis for the application of CAP in the disinfection of biofilms.

摘要

耐多药细菌形成的生物膜是医院获得性感染的主要原因。冷大气压等离子体(CAP)在杀菌方面具有吸引力,尤其对于破坏耐多药细菌形成的生物膜。然而,其潜在的分子机制尚不清楚。在本研究中,CAP有效减少了耐甲氧西林金黄色葡萄球菌形成的生物膜中的活细胞,用CAP处理6分钟可使生物膜中的细胞减少3.5个对数级。CAP处理导致生物膜细胞中SaFtsZ和SaClpP蛋白聚合。体外分析表明,用CAP处理2分钟后,重组SaFtsZ失去了自组装能力,重组SaClpP失去了肽酶活性。质谱显示,CAP的活性物质诱导了一系列相差16 Da、31 Da、32 Da、47 Da、48 Da、62 Da和78 Da的峰的氧化修饰。推测CAP诱导了生物膜细胞中蛋白质的氧化损伤,这有助于生物膜的减少。本研究阐明了CAP对生物膜细菌细胞中蛋白质的生物学效应,并为CAP在生物膜消毒中的应用提供了依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/553f/8156483/d76ee50ad115/microorganisms-09-01072-g001.jpg

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