首页> 外文期刊>Revista Argentina de Microbiologia >Ultrastructural changes in methicillin-resistant Staphylococcus aureus (MRSA) induced by a novel cyclic peptide ASP-1 from Bacillus subtilis: A scanning electron microscopy (SEM) study
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Ultrastructural changes in methicillin-resistant Staphylococcus aureus (MRSA) induced by a novel cyclic peptide ASP-1 from Bacillus subtilis: A scanning electron microscopy (SEM) study

机译:耐甲氧西林的超微结构变化金黄色葡萄球菌(MRSA)由新的环状肽Asp-1引起的芽孢杆菌:扫描电子显微镜 (SEM)研究

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Increasing antimicrobial resistance amongStaphylococcus aureusnecessitates a new antimicrobial with a different site of action. We have isolated a novel cyclic peptide-1 (ASP-1) fromBacillussubtiliswith potent activity against methicillin-resistantS. aureus(MRSA) at a minimum inhibitory concentration (MIC) of 8–64μg/ml. Scanning electron micrographs demonstrated drastic changes in the cellular architecture of ASP-1 treated cells ofS. aureusATCC 29213 and an MRSA clinical isolate at MICs, with damages to the cell wall, membrane lysis and probable leakage of cytoplasmic contents at minimum bactericidal concentrations. The ultrastructure alterations induced by ASP-1 have also been compared with those of oxacillin-treated MRSA cells at its MIC using scanning electron microscopy.
机译:增加抗菌药物之间的抗菌药物,AUREUSNEENTINATINE具有不同的行动部位的新抗菌药物。 我们已经孤立新的循环肽-1(ASP-1)FrobBacillussubtiliswith抗甲氧西林抗性活性。 金黄色葡萄球菌(MRSA)在最小抑制浓度(MIC)为8-64μg/ ml。 扫描电子显微照片显示了ASP-1处理细胞的蜂窝结构中的剧烈变化。 AUREUSATCC 29213和MICS的MRSA临床分离物,损坏细胞壁,膜裂解和在最小杀菌浓度下的细胞质含量泄漏。 也将ASP-1诱导的超微结构改变与使用扫描电子显微镜的MIC在其MIC处的牛奶蛋白处理的MRSA细胞的超微结构改变。

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