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抗菌光动力失活作为一种通过微调CpxRA双组分系统的活性来抑制[具体细菌名称未给出]生长的替代方法。

Antimicrobial photodynamic inactivation as an alternative approach to inhibit the growth of by fine-tuning the activity of CpxRA two-component system.

作者信息

Xu Jinchun, Yao Huangbing, Li Yali, Liao Qiaoming, Wan Xiaoxiao, Liu Lulu, Ma Xiaojing, Tao Han, Wang Hui-Li, Xu Yi

机构信息

School of Food Science and Bioengineering, Hefei University of Technology, Hefei, China.

出版信息

Front Microbiol. 2023 Jan 17;13:1063425. doi: 10.3389/fmicb.2022.1063425. eCollection 2022.

Abstract

is an opportunistic foodborne pathogen primarily found in powdered infant formula (PIF). To date, it remains challenging to control the growth of this ubiquitous bacterium. Herein, antimicrobial photodynamic inactivation (aPDI) was first employed to inactivate . Through 460 nm light irradiation coupled with hypocrellin B, the survival rate of was diminished by 34 log. The photokilling effect was mediated by the attenuated membrane integrity, as evidenced by PI staining. Besides, scanning electron microscopy showed the deformed and aggregated cell cluster, and intracellular ROS was augmented by 23 folds when light doses increase. In addition to planktonic cells, the biofilm formation of was also affected, showing an OD decline from 0.85 to 0.25. In terms of molecular aspects, a two-component system called CpxRA, along with their target genes, was deregulated during illumination. Using the knock-out strain of ΔCpxA, the bacterial viability was reduced by 2 log under aPDI, a wider gap than the wildtype strain. Based on the promoted expression of and , aPDI is likely to play its part through attenuating the function of CpxRA-OmpC pathway. Finally, the aPDI system was applied to PIF, and was inactivated under various desiccated or heated storage conditions. Collectively, aPDI serves as an alternative approach to decontaminate , providing a new strategy to reduce the health risks caused by this prevalent foodborne pathogen.

摘要

是一种主要存在于婴儿配方奶粉(PIF)中的食源性机会致病菌。迄今为止,控制这种普遍存在的细菌的生长仍然具有挑战性。在此,首次采用抗菌光动力灭活(aPDI)来灭活 。通过460纳米光照射结合竹红菌素B, 的存活率降低了3至4个对数。PI染色证明,光杀伤作用是由膜完整性减弱介导的。此外,扫描电子显微镜显示细胞簇变形和聚集,当光剂量增加时,细胞内活性氧增加2至3倍。除了浮游细胞外, 的生物膜形成也受到影响,其光密度从0.85降至0.25。在分子方面,一种名为CpxRA的双组分系统及其靶基因在光照过程中被失调。使用ΔCpxA基因敲除菌株,在aPDI作用下细菌活力降低了2个对数,比野生型菌株的差距更大。基于 和 的表达上调,aPDI可能通过减弱CpxRA - OmpC途径的功能发挥作用。最后,将aPDI系统应用于PIF,并且在各种干燥或加热储存条件下 被灭活。总的来说,aPDI作为一种替代方法对 进行去污,为降低这种普遍存在的食源性病原菌引起的健康风险提供了一种新策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f169/9886882/2d5865277a92/fmicb-13-1063425-g001.jpg

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