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柯里拉京和tellimagrandin I的作用机制,它们能显著增强β-内酰胺类药物对耐甲氧西林金黄色葡萄球菌的活性。

Mechanisms of action of corilagin and tellimagrandin I that remarkably potentiate the activity of beta-lactams against methicillin-resistant Staphylococcus aureus.

作者信息

Shiota Sumiko, Shimizu Masato, Sugiyama Jun'ichi, Morita Yuji, Mizushima Tohru, Tsuchiya Tomofusa

机构信息

Department of Pathogenic Microbiology, School of Pharmacy, Shujitsu University, Okayama, Japan.

出版信息

Microbiol Immunol. 2004;48(1):67-73. doi: 10.1111/j.1348-0421.2004.tb03489.x.

Abstract

Corilagin and tellimagrandin I are polyphenols isolated from the extract of Arctostaphylos uvaursi and Rosa canina L. (rose red), respectively. We have reported that corilagin and tellimagrandin I remarkably reduced the minimum inhibitory concentration (MIC) of beta-lactams in methicillin-resistant Staphylococcus aureus(MRSA). In this study, we investigated the effect of corilagin and tellimagrandin I on the penicillin binding protein 2 '(2a) (PBP2 '(PBP2a)) which mainly confers the resistance to beta-lactam antibiotics in MRSA. These compounds when added to the culture medium were found to decrease production of the PBP2 '(PBP2a) slightly. Using BOCILLIN FL, a fluorescent-labeled benzyl penicillin, we found that PBP2 '(PBP2a) in MRSA cells that were grown in medium containing corilagin or tellimagrandin I almost completely lost the ability to bind BOCILLIN FL. The binding activity of PBP2 and PBP3 were also reduced to some extent by these compounds. These results indicate that inactivation of PBPs, especially of PBP2 '(PBP2a), by corilagin or tellimagrandin I is the major reason for the remarkable reduction in the resistance level of beta-lactams in MRSA. Corilagin or tellimagrandin I suppressed the activity of beta-lactamase to some extent.

摘要

柯里拉京和tellimagrandin I分别是从熊果叶提取物和犬蔷薇(玫瑰红)中分离出的多酚类物质。我们曾报道,柯里拉京和tellimagrandin I能显著降低耐甲氧西林金黄色葡萄球菌(MRSA)中β-内酰胺类抗生素的最低抑菌浓度(MIC)。在本研究中,我们研究了柯里拉京和tellimagrandin I对青霉素结合蛋白2'(2a)(PBP2'(PBP2a))的影响,该蛋白主要赋予MRSA对β-内酰胺类抗生素的耐药性。当将这些化合物添加到培养基中时,发现它们会略微降低PBP2'(PBP2a)的产生。使用荧光标记的苄青霉素BOCILLIN FL,我们发现,在含有柯里拉京或tellimagrandin I的培养基中生长的MRSA细胞中的PBP2'(PBP2a)几乎完全丧失了结合BOCILLIN FL的能力。这些化合物也会在一定程度上降低PBP2和PBP3的结合活性。这些结果表明,柯里拉京或tellimagrandin I使PBPs失活,尤其是PBP2'(PBP2a),是MRSA中β-内酰胺类抗生素耐药水平显著降低的主要原因。柯里拉京或tellimagrandin I在一定程度上抑制了β-内酰胺酶的活性。

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