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首页> 外文期刊>Frontiers in Microbiology >Anti-staphylococcus Antibiotics Interfere With the Transcription of Leucocidin ED Gene in Staphylococcus aureus Strain Newman
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Anti-staphylococcus Antibiotics Interfere With the Transcription of Leucocidin ED Gene in Staphylococcus aureus Strain Newman

机译:抗葡萄球菌抗生素干扰了<斜晶蛋白ED基因的转录<斜斜葡萄球菌(金黄色葡萄球菌)拉力纽曼

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摘要

Antibiotics have been described to modulate bacterial virulence gene expression. This study aimed to assess the changes caused by anti- Staphylococcus agents in the transcription of leucocidin ED ( lukED ) gene of Staphylococcus aureus strain Newman in vitro and in vivo and to determine whether the altered expression is agr dependent. The bacteria were exposed to subinhibitory concentrations [1/2, 1/4, or 1/8 minimal inhibitory concentration (MIC)] of 11 antibiotics, and the expression of lukE and agr -effector RNAIII was determined using qRT-PCR. In vivo experiments were performed to evaluate the impact exerted by six representative antibiotics on the transcription of both genes. Molecular analysis showed that in vitro lukE transcription was dramatically promoted in the Newman strain exposed to sub-MICs of vancomycin, trimethoprim–sulfamethoxazole, clindamycin, gentamicin, daptomycin, and ciprofloxacin and considerably reduced when stimulated by cefazolin, erythromycin, rifampicin, tigecycline, and linezolid. In the murine abscess model, tigecycline significantly decreased the transcription of lukE and the bacterial numbers, whereas vancomycin increased them; although cefazolin increased the lukE expression (contrary to the in vitro effect), it had a remarkable role in reducing bacterial load. The correspondence analysis shows that RNAIII expression varied under seven of 11 antibiotics in vitro , and six drugs in vivo were consistent with lukE transcripts. In conclusion, our data show that anti- Staphylococcus antibiotics exert modulatory effects on lukE expression in vitro and/or in vivo , and the changed expression caused by some drugs may be involved with agr activity, thus providing a guide to choose appropriate agents to avoid promoting bacterial virulence in lukED -positive S. aureus infections.
机译:已描述抗生素来调节细菌毒力基因表达。本研究旨在评估体外和体内葡萄球菌菌株纽曼的白昔甙Ed(Luked)基因转录的抗葡聚糖蛋白(Luked)基因转录的变化,并确定改变的表达是否依赖于植物。将细菌暴露于11种抗生素的后抑制浓度[1/2,1 / 4,或1/8最小抑制浓度(MIC)],使用QRT-PCR测定Luke和Agr-yefectorRNaiII的表达。进行体内实验以评估六种代表性抗生素对两种基因的转录施加的影响。分子分析表明,在纽曼菌株中暴露于万古霉素,三甲双胍,磺胺嘧啶,甘氨酸,丁染蛋白和环丙沙星的亚麦克风中,在纽曼菌株中促进了体外转录,并且当由Cefazolin,红霉素,利福平,脱癸锌苷刺激时显着减少linezolid。在鼠脓肿模型中,脱癸素素显着降低了洛克和细菌数的转录,而万古霉素增加了它们;虽然Cefazolin增加了Luke表达(与体外效应相反),但它在减少细菌载荷方面具有显着作用。对应分析表明,在体外六种抗生素中的7个抗生素中的七种表达和体内六种药物与促糖转录物一致。总之,我们的数据显示,抗葡萄球菌抗生素在体外和/或体内对促糖表达产生调节作用,并且由某些药物引起的改变的表达可能涉及农业活动,从而提供指导选择适当的药剂以避免促进Luked-阳阳性S. aureus感染中的细菌毒力。

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