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源自海洋海绵的sp. SBT343提取物可抑制葡萄球菌生物膜形成。

Marine Sponge-Derived sp. SBT343 Extract Inhibits Staphylococcal Biofilm Formation.

作者信息

Balasubramanian Srikkanth, Othman Eman M, Kampik Daniel, Stopper Helga, Hentschel Ute, Ziebuhr Wilma, Oelschlaeger Tobias A, Abdelmohsen Usama R

机构信息

Institute for Molecular Infection Biology, University of Würzburg Würzburg, Germany.

Institute of Pharmacology and Toxicology, University of WürzburgWürzburg, Germany; Department of Analytical Chemistry, Faculty of Pharmacy, Minia UniversityMinia, Egypt.

出版信息

Front Microbiol. 2017 Feb 16;8:236. doi: 10.3389/fmicb.2017.00236. eCollection 2017.

Abstract

and are opportunistic pathogens that cause nosocomial and chronic biofilm-associated infections. Indwelling medical devices and contact lenses are ideal ecological niches for formation of staphylococcal biofilms. Bacteria within biofilms are known to display reduced susceptibilities to antimicrobials and are protected from the host immune system. High rates of acquired antibiotic resistances in staphylococci and other biofilm-forming bacteria further hamper treatment options and highlight the need for new anti-biofilm strategies. Here, we aimed to evaluate the potential of marine sponge-derived actinomycetes in inhibiting biofilm formation of several strains of , and Results from biofilm-formation assays, as well as scanning electron and confocal microscopy, revealed that an organic extract derived from the marine sponge-associated bacterium sp. SBT343 significantly inhibited staphylococcal biofilm formation on polystyrene, glass and contact lens surfaces, without affecting bacterial growth. The extract also displayed similar antagonistic effects towards the biofilm formation of other and strains tested but had no inhibitory effects towards biofilms. Interestingly the extract, at lower effective concentrations, did not exhibit cytotoxic effects on mouse fibroblast, macrophage and human corneal epithelial cell lines. Chemical analysis by High Resolution Fourier Transform Mass Spectrometry (HRMS) of the sp. SBT343 extract proportion revealed its chemical richness and complexity. Preliminary physico-chemical characterization of the extract highlighted the heat-stable and non-proteinaceous nature of the active component(s). The combined data suggest that the sp. SBT343 extract selectively inhibits staphylococcal biofilm formation without interfering with bacterial cell viability. Due to absence of cell toxicity, the extract might represent a good starting material to develop a future remedy to block staphylococcal biofilm formation on contact lenses and thereby to prevent intractable contact lens-mediated ocular infections.

摘要

[细菌名称1]和[细菌名称2]是引起医院感染和慢性生物膜相关感染的机会致病菌。植入式医疗设备和隐形眼镜是葡萄球菌生物膜形成的理想生态位。已知生物膜内的细菌对抗微生物药物的敏感性降低,并受到宿主免疫系统的保护。葡萄球菌和其他形成生物膜的细菌中获得性抗生素耐药率很高,这进一步阻碍了治疗选择,并凸显了新的抗生物膜策略的必要性。在此,我们旨在评估海洋海绵来源的放线菌抑制[细菌名称1]、[细菌名称2]和[细菌名称3]几株菌株生物膜形成的潜力。[细菌名称1]生物膜形成试验以及扫描电子显微镜和共聚焦显微镜的结果表明,源自海洋海绵相关细菌[细菌名称4] sp. SBT343的有机提取物显著抑制葡萄球菌在聚苯乙烯、玻璃和隐形眼镜表面的生物膜形成,而不影响细菌生长。该提取物对其他测试的[细菌名称1]和[细菌名称2]菌株的生物膜形成也表现出类似的拮抗作用,但对[细菌名称3]生物膜没有抑制作用。有趣的是,该提取物在较低有效浓度下对小鼠成纤维细胞、巨噬细胞和人角膜上皮细胞系没有细胞毒性作用。通过高分辨率傅里叶变换质谱(HRMS)对[细菌名称4] sp. SBT343提取物成分进行化学分析,揭示了其化学丰富性和复杂性。提取物的初步物理化学特性突出了活性成分的热稳定性和非蛋白质性质。综合数据表明,[细菌名称4] sp. SBT343提取物选择性抑制葡萄球菌生物膜形成,而不干扰细菌细胞活力。由于没有细胞毒性,该提取物可能是开发未来阻断隐形眼镜上葡萄球菌生物膜形成从而预防难治性隐形眼镜介导的眼部感染的良好起始材料。

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