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果皮提取物对属于ESKAPE组病原体的抗菌效果。

Antimicrobial efficacy of peel extract against pathogens belonging to the ESKAPE group.

作者信息

Scaglione Elena, Sateriale Daniela, Mantova Giuseppe, Di Rosario Martina, Continisio Leonardo, Vitiello Mariateresa, Pagliarulo Caterina, Colicchio Roberta, Pagliuca Chiara, Salvatore Paola

机构信息

Department of Molecular Medicine and Medical Biotechnologies, University of Naples Federico II, Naples, Italy.

Department of Science and Technology, University of Sannio, Benevento, Italy.

出版信息

Front Microbiol. 2024 Apr 22;15:1383027. doi: 10.3389/fmicb.2024.1383027. eCollection 2024.

DOI:10.3389/fmicb.2024.1383027
PMID:38711969
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11070501/
Abstract

The improper use and abuse of antibiotics have led to an increase in multidrug-resistant (MDR) bacteria resulting in a failure of standard antibiotic therapies. To date, this phenomenon represents a leading public health threat of the 21st century which requires alternative strategies to fight infections such as the identification of new molecules active against MDR strains. In the last 20 years, natural extracts with biological activities attracted scientific interest. Following the One Health Approach, natural by-products represent a sustainable and promising alternative solution. Consistently, the aim of the present study was to evaluate the antimicrobial activity of hydro-alcoholic pomegranate peel extract (PPE) against MDR microorganisms belonging to , , , , and spp. "ESKAPE" group pathogens. Through semiquantitative and quantitative methods, the PPE showed effective antimicrobial activity against Gram-positive and Gram-negative MDR bacteria. The kinetics of bactericidal action of PPE highlighted that microbial death was achieved in a time- and dose-dependent manner. High concentrations of PPE exhibited antioxidant activity, providing a protective effect on cellular systems and red blood cell membranes. Finally, we report, for the first time, a significant intracellular antibacterial property of PPE as highlighted by its bactericidal action against the staphylococcal reference strain and its bacteriostatic effect against clinical resistant strain in the HeLa cell line. In conclusion, due to its characterized content of polyphenolic compounds and antioxidant activity strength, the PPE could be considered as a therapeutic agent alone or in conjunction with standard antibiotics against challenging infections caused by ESKAPE pathogens.

摘要

抗生素的不当使用和滥用导致了多重耐药(MDR)细菌的增加,致使标准抗生素疗法失效。迄今为止,这种现象是21世纪主要的公共卫生威胁之一,需要采用替代策略来对抗感染,比如鉴定对MDR菌株有活性的新分子。在过去20年里,具有生物活性的天然提取物引起了科学界的关注。遵循“同一健康”方法,天然副产品是一种可持续且有前景的替代解决方案。同样地,本研究的目的是评估石榴皮水醇提取物(PPE)对属于“ESKAPE”组病原体的MDR微生物(分别为金黄色葡萄球菌、肺炎克雷伯菌、鲍曼不动杆菌、粪肠球菌、铜绿假单胞菌和阴沟肠杆菌)的抗菌活性。通过半定量和定量方法,PPE对革兰氏阳性和革兰氏阴性MDR细菌均表现出有效的抗菌活性。PPE杀菌作用的动力学表明,微生物死亡呈时间和剂量依赖性。高浓度的PPE表现出抗氧化活性,对细胞系统和红细胞膜具有保护作用。最后,我们首次报道了PPE具有显著的细胞内抗菌特性,这体现在它对金黄色葡萄球菌参考菌株的杀菌作用以及对HeLa细胞系中临床耐药菌株的抑菌作用上。总之,由于其特有的多酚类化合物含量和抗氧化活性强度,PPE可单独或与标准抗生素联合使用,作为治疗由ESKAPE病原体引起的挑战性感染的治疗剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abf1/11070501/269899253765/fmicb-15-1383027-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abf1/11070501/78385b5c866b/fmicb-15-1383027-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abf1/11070501/d1ddf5f209d3/fmicb-15-1383027-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abf1/11070501/175a70f9a659/fmicb-15-1383027-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abf1/11070501/c7d42d3cbbc4/fmicb-15-1383027-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abf1/11070501/fed2a0742564/fmicb-15-1383027-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abf1/11070501/269899253765/fmicb-15-1383027-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abf1/11070501/78385b5c866b/fmicb-15-1383027-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abf1/11070501/d1ddf5f209d3/fmicb-15-1383027-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abf1/11070501/175a70f9a659/fmicb-15-1383027-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abf1/11070501/c7d42d3cbbc4/fmicb-15-1383027-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abf1/11070501/fed2a0742564/fmicb-15-1383027-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abf1/11070501/269899253765/fmicb-15-1383027-g006.jpg

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