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鲨胺和克拉胺A1可分散生物膜。

Squalamine and claramine A1 disperse biofilm.

作者信息

Tareau Anne-Sophie, Tahrioui Ali, Gonzalez Mathieu, Croize Evan, Varin Simon Jennifer, Barreau Magalie, David Audrey, Reffuveille Fany, Brunel Jean-Michel, Lesouhaitier Olivier, Chevalier Sylvie

机构信息

Univ Rouen Normandie, Université Caen Normandie, Normandie Univ, CBSA UR 4312, F-76000, Rouen, France.

Univ Rouen Normandie, Platform of Sanitary Safety, Evreux Campus, PS2E, France.

出版信息

Biofilm. 2025 May 27;9:100293. doi: 10.1016/j.bioflm.2025.100293. eCollection 2025 Jun.

DOI:10.1016/j.bioflm.2025.100293
PMID:40519941
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12166708/
Abstract

is an opportunistic pathogen that causes both acute and chronic infections, including pneumonia, bloodstream infections, urinary tract infections, and surgical site infections. It poses a significant threat to individuals with chronic lung conditions, particularly those with cystic fibrosis. Squalamine and claramine A1 have emerged as promising antibacterial compounds, exhibiting activity against a broad range of both Gram-positive and Gram-negative bacteria. Beyond their potent antibacterial properties, our findings reveal that sub-inhibitory concentrations of claramine A1 and squalamine can disperse pre-formed biofilm without impacting bacterial growth. While claramine A1, but not squalamine, enhances membrane fluidity, the structural difference between these compounds lies primarily in their spermine and spermidine moieties. Notably, we found that spermine, unlike spermidine, was able to both disperse biofilm and increase membrane fluidity. Together, our results suggest that while both compounds are effective at disrupting biofilm, they likely act through distinct mechanisms.

摘要

是一种机会致病菌,可引起急性和慢性感染,包括肺炎、血流感染、尿路感染和手术部位感染。它对患有慢性肺部疾病的个体构成重大威胁,尤其是那些患有囊性纤维化的个体。鲨胺和克拉胺A1已成为有前景的抗菌化合物,对多种革兰氏阳性菌和革兰氏阴性菌均有活性。除了其强大的抗菌特性外,我们的研究结果表明,亚抑制浓度的克拉胺A1和鲨胺可以分散预先形成的生物膜,而不影响细菌生长。虽然克拉胺A1而非鲨胺可增强膜流动性,但这些化合物之间的结构差异主要在于它们的精胺和亚精胺部分。值得注意的是,我们发现精胺与亚精胺不同,它既能分散生物膜又能增加膜流动性。总之,我们的结果表明,虽然这两种化合物在破坏生物膜方面都有效,但它们可能通过不同的机制起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6e8/12166708/f2f9fda2700c/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6e8/12166708/b6af666b3a21/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6e8/12166708/bc70ed0d9845/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6e8/12166708/9086cef77d26/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6e8/12166708/bd0f755af5f5/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6e8/12166708/f1c0faf8a4c3/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6e8/12166708/f2f9fda2700c/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6e8/12166708/b6af666b3a21/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6e8/12166708/bc70ed0d9845/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6e8/12166708/9086cef77d26/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6e8/12166708/bd0f755af5f5/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6e8/12166708/f1c0faf8a4c3/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6e8/12166708/f2f9fda2700c/gr6.jpg

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本文引用的文献

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A new model of endotracheal tube biofilm identifies combinations of matrix-degrading enzymes and antimicrobials able to eradicate biofilms of pathogens that cause ventilator-associated pneumonia.一种新型气管内导管生物膜模型确定了能够根除引起呼吸机相关性肺炎病原体生物膜的基质降解酶和抗菌药物的组合。
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Membrane fluidity homeostasis is required for tobramycin-enhanced biofilm in .
膜流动性的内稳态对于妥布霉素增强生物膜是必需的。
Microbiol Spectr. 2024 Apr 2;12(4):e0230323. doi: 10.1128/spectrum.02303-23. Epub 2024 Feb 27.
4
Repurposing DNase I and alginate lyase to degrade the biofilm matrix of dual-species biofilms of Staphylococcus aureus and Pseudomonas aeruginosa grown in artificial sputum medium: In-vitro assessment of their activity in combination with broad-spectrum antibiotics.重新利用脱氧核糖核酸酶I和海藻酸裂解酶来降解在人工痰液培养基中生长的金黄色葡萄球菌和铜绿假单胞菌双物种生物膜的生物膜基质:对它们与广谱抗生素联合使用时活性的体外评估
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