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人肝脏来源的抗菌肽 Hepcidin 20 对表皮葡萄球菌多糖细胞间黏附素(PIA)阳性和 PIA 阴性菌株生物膜的抑制作用。

Inhibitory effect of the human liver-derived antimicrobial peptide hepcidin 20 on biofilms of polysaccharide intercellular adhesin (PIA)-positive and PIA-negative strains of Staphylococcus epidermidis.

作者信息

Brancatisano Franca Lisa, Maisetta Giuseppantonio, Di Luca Mariagrazia, Esin Semih, Bottai Daria, Bizzarri Ranieri, Campa Mario, Batoni Giovanna

机构信息

a Department of Translational Research and new Technologies in Medicine and Surgery , University of Pisa , via S. Zeno 35-39, 56127 Pisa , Italy.

出版信息

Biofouling. 2014;30(4):435-46. doi: 10.1080/08927014.2014.888062. Epub 2014 Mar 19.

Abstract

Staphylococcus epidermidis plays a major role in biofilm-related medical device infections. Herein the anti-biofilm activity of the human liver-derived antimicrobial peptide hepcidin 20 (hep20) was evaluated against polysaccharide intercellular adhesin (PIA)-positive and PIA-negative clinical isolates of S. epidermidis. Hep20 markedly inhibited biofilm formation and bacterial cell metabolism of PIA-positive and PIA-negative strains, but the decrease in biofilm biomass only partially correlated with a decrease in viable bacteria. Confocal microscope images revealed that, in the presence of hep20, both PIA-positive and PIA-negative strains formed biofilms with altered architectures and reduced amounts of extracellular matrix. Co-incubation of hep20 with vancomycin produced no synergistic effect, evaluated as number of viable cells, both in preventing biofilm formation and in treating preformed biofilms. In contrast, biofilms obtained in the presence of hep20, and then exposed to vancomycin, displayed an increased susceptibility to vancomycin. These results suggest that hep20 may inhibit the production/accumulation of biofilm extracellular matrix.

摘要

表皮葡萄球菌在与生物膜相关的医疗器械感染中起主要作用。在此,评估了人肝脏来源的抗菌肽铁调素20(hep20)对表皮葡萄球菌多糖细胞间黏附素(PIA)阳性和PIA阴性临床分离株的抗生物膜活性。Hep20显著抑制PIA阳性和PIA阴性菌株的生物膜形成和细菌细胞代谢,但生物膜生物量的减少仅部分与活菌数量的减少相关。共聚焦显微镜图像显示,在hep20存在的情况下,PIA阳性和PIA阴性菌株形成的生物膜结构改变,细胞外基质数量减少。Hep20与万古霉素共同孵育在预防生物膜形成和治疗预先形成的生物膜方面,以活菌数量评估均未产生协同作用。相反,在hep20存在下形成的生物膜,然后暴露于万古霉素,对万古霉素的敏感性增加。这些结果表明,hep20可能抑制生物膜细胞外基质的产生/积累。

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