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用防御素IB-367进行预处理可影响革兰氏阳性生物膜,并增强利奈唑胺在中心静脉导管感染动物模型中的治疗效果。

Pretreatment with the protegrin IB-367 affects Gram-positive biofilm and enhances the therapeutic efficacy of linezolid in animal models of central venous catheter infection.

作者信息

Ghiselli Roberto, Giacometti Andrea, Cirioni Oscar, Mocchegiani Federico, Silvestri Carmela, Orlando Fiorenza, Kamysz Wojciech, Licci Alberto, Nadolski Piotr, Della Vittoria Agnese, Łukasiak Jerzy, Scalise Giorgio, Saba Vittorio

机构信息

Department of General Surgery, I.N.R.C.A. I.R.R.C.S., Università Politecnica delle Marche, Ancona, Italy.

出版信息

JPEN J Parenter Enteral Nutr. 2007 Nov-Dec;31(6):463-8. doi: 10.1177/0148607107031006463.

Abstract

BACKGROUND

Biofilms play an important role in the pathogenesis of several chronic infections and nosocomial infections related to indwelling medical devices.

METHODS

To assess the efficacy of IB-367 and linezolid (LZD) in the treatment of central venous catheter (CVC) infections using the antibiotic-lock technique, in vitro and in vivo studies were performed. The in vitro antibiotic susceptibility assay for Staphylococcus aureus and Enterococcus faecalis biofilms developed on 96-well polystyrene tissue culture plates was performed to determine the activity of the compounds. Efficacy studies were performed in rat models of Gram-positive CVC infection. Silastic catheters were implanted into the superior cava of adult male Wistar rats. Twenty-four hours after implantation, the catheters were pretreated by filling with IB-367. Thirty minutes later, rats were challenged via the CVC with 1.0 x 10(6) CFU (colony forming units) of S aureus strain diffuse Smith and clinical isolate of slime-producing E faecalis. Administration of LZD into the CVC at a concentration equal to the minimum bacteriocidal concentration observed using adherent cells or at a much higher concentration (1024 microg/mL) began 24 hours later.

RESULTS

Both for S aureus and E faecalis, the killing activities of LZD against adherent bacteria were at least 4-fold to 8-fold lower than that against freely growing cells. For both strains, in IB-367-pretreated wells, LZD strongly increases its activity. The in vivo studies showed that when CVCs were pretreated with IB-367, Gram-positive biofilm bacterial load was further decreased to 10(1) CFU/mL and bacteremia was not detected.

CONCLUSIONS

IB-367 has potential as an adjunctive agent to LZD in the treatment of Gram-positive biofilm infections such as CVC infections.

摘要

背景

生物膜在几种慢性感染以及与留置医疗器械相关的医院感染的发病机制中起重要作用。

方法

为了使用抗生素封管技术评估IB-367和利奈唑胺(LZD)治疗中心静脉导管(CVC)感染的疗效,进行了体外和体内研究。在96孔聚苯乙烯组织培养板上对金黄色葡萄球菌和粪肠球菌生物膜进行体外抗生素敏感性试验,以确定这些化合物的活性。在革兰氏阳性CVC感染的大鼠模型中进行疗效研究。将硅橡胶导管植入成年雄性Wistar大鼠的上腔静脉。植入后24小时,通过向导管内注入IB-367进行预处理。30分钟后,经CVC用1.0×10⁶CFU(菌落形成单位)的金黄色葡萄球菌菌株弥漫史密斯株和产黏液粪肠球菌临床分离株对大鼠进行攻击。24小时后开始以等于使用贴壁细胞观察到的最低杀菌浓度或更高得多的浓度(1024μg/mL)向CVC内注入LZD。

结果

对于金黄色葡萄球菌和粪肠球菌,LZD对贴壁细菌的杀灭活性比对自由生长细胞的杀灭活性至少低4倍至8倍。对于这两种菌株,在经IB-367预处理的孔中,LZD的活性显著增强。体内研究表明,当用IB-367对CVC进行预处理时,革兰氏阳性生物膜细菌载量进一步降至10¹CFU/mL,且未检测到菌血症。

结论

在治疗革兰氏阳性生物膜感染如CVC感染方面,IB-367有潜力作为LZD的辅助药物。

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