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芦丁载壳聚糖纳米粒抗致病性金黄色葡萄球菌的抗毒力活性。

Antivirulence activities of Rutin-loaded chitosan nanoparticles against pathogenic Staphylococcus aureus.

机构信息

Department of Biology, Lahijan Branch, Islamic Azad University, Lahijan, Iran.

Department of Microbiology, Lahijan Branch, Islamic Azad University, Lahijan, Iran.

出版信息

BMC Microbiol. 2024 Sep 7;24(1):328. doi: 10.1186/s12866-024-03446-7.

DOI:10.1186/s12866-024-03446-7
PMID:39244527
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11380343/
Abstract

BACKGROUND

Staphylococcus aureus is an infectious bacterium that is frequently found in healthcare settings and the community. This study aimed to prepare rutin-loaded chitosan nanoparticles (Rut-CS NPs) and assess their antibacterial activity against pathogenic strains of S. aureus.

RESULTS

The synthesized Rut-CS NPs exhibited an amorphous morphology with a size ranging from 160 to 240 nm and a zeta potential of 37.3 mV. Rut-CS NPs demonstrated significant antibacterial activity against S. aureus strains. Following exposure to Rut-CS NPs, the production of staphyloxanthin pigment decreased by 43.31-89.63%, leading to increased susceptibility of S. aureus to hydrogen peroxide. Additionally, visual inspection of cell morphology indicated changes in membrane integrity and permeability upon Rut-CS NPs exposure, leading to a substantial increase (107.07-191.08%) in cytoplasmic DNA leakage in the strains. Furthermore, ½ MIC of Rut-CS NPs effectively inhibited the biofilm formation (22.5-37.5%) and hemolytic activity (69-82.59%) in the S. aureus strains.

CONCLUSIONS

Our study showcases that Rut-CS NPs can serve as a novel treatment agent to combat S. aureus infections by altering cell morphology and inhibiting virulence factors of S. aureus.

摘要

背景

金黄色葡萄球菌是一种常见的感染性细菌,存在于医疗保健环境和社区中。本研究旨在制备载芦丁壳聚糖纳米粒(Rut-CS NPs),并评估其对金黄色葡萄球菌致病株的抗菌活性。

结果

合成的 Rut-CS NPs 呈无定形形态,粒径为 160-240nm,zeta 电位为 37.3mV。Rut-CS NPs 对金黄色葡萄球菌菌株表现出显著的抗菌活性。暴露于 Rut-CS NPs 后,金黄色葡萄球菌色素产量下降了 43.31-89.63%,使其对过氧化氢的敏感性增加。此外,细胞形态的直观观察表明,细胞膜完整性和通透性在 Rut-CS NPs 暴露后发生变化,导致菌株细胞质 DNA 泄漏增加 107.07-191.08%。此外,Rut-CS NPs 的 ½ MIC 有效抑制了金黄色葡萄球菌菌株的生物膜形成(22.5-37.5%)和溶血活性(69-82.59%)。

结论

我们的研究表明,Rut-CS NPs 可以通过改变细胞形态和抑制金黄色葡萄球菌的毒力因子,成为一种新型的治疗金黄色葡萄球菌感染的药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/baaa/11380343/c80375efb6f1/12866_2024_3446_Fig13_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/baaa/11380343/f0c82572a42e/12866_2024_3446_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/baaa/11380343/142a2e0789e7/12866_2024_3446_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/baaa/11380343/f477497e176d/12866_2024_3446_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/baaa/11380343/ee4a4549cacf/12866_2024_3446_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/baaa/11380343/72961566f3da/12866_2024_3446_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/baaa/11380343/41e31b88fce5/12866_2024_3446_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/baaa/11380343/b8d3e3db9b5b/12866_2024_3446_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/baaa/11380343/cc68d8ae6a5c/12866_2024_3446_Fig11_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/baaa/11380343/0e43c2520d60/12866_2024_3446_Fig12_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/baaa/11380343/c80375efb6f1/12866_2024_3446_Fig13_HTML.jpg

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