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利福平辅助治疗增加 A 组链球菌组织感染模型中的抗生素疗效。

Adjunctive Rifampicin Increases Antibiotic Efficacy in Group A Streptococcal Tissue Infection Models.

机构信息

Center for Infectious Medicine, Karolinska Institutet, Karolinska University Hospital Huddinge, Stockholm, Sweden.

Royal Devon and Exeter Hospital, Exeter, United Kingdom.

出版信息

Antimicrob Agents Chemother. 2021 Oct 18;65(11):e0065821. doi: 10.1128/AAC.00658-21. Epub 2021 Sep 7.

Abstract

Biofilm has recently been highlighted as a complicating feature of necrotizing soft tissue infections (NSTI) caused by Streptococcus pyogenes (i.e., group A Streptococcus [GAS]) contributing to a persistence of bacteria in tissue despite prolonged antibiotic therapy. Here, we assessed the standard treatment of benzylpenicillin and clindamycin with or without rifampin in a tissue-like setting. Antibiotic efficacy was evaluated by CFU determination in a human organotypic skin model infected for 24 or 48 h with GAS strains isolated from NSTI patients. Antibiotic effect was also evaluated by microcalorimetric metabolic assessment in infections of cellular monolayers providing continuous measurements over time. Adjunctive rifampin resulted in enhanced antibiotic efficacy of bacterial clearance in an organotypic skin tissue model, 97.5% versus 93.9% ( = 0.006). Through microcalorimetric measurements, adjunctive rifampin resulted in decreased metabolic activity and extended lag phase for all clinical GAS strains tested ( < 0.05). In addition, a case report is presented of adjunctive rifampin treatment in an NSTI case with persistent GAS tissue infection. The findings of this study demonstrate that adjunctive rifampin enhances clearance of GAS biofilm in an tissue infection model.

摘要

生物膜最近被强调为化脓性链球菌(即 A 组链球菌(GAS))引起的坏死性软组织感染(NSTI)的一个复杂特征,尽管长期使用抗生素治疗,但仍导致细菌在组织中持续存在。在这里,我们在类似组织的环境中评估了苯唑西林和克林霉素联合或不联合利福平的标准治疗。通过在感染 GAS 菌株 24 或 48 小时的人体器官型皮肤模型中进行 CFU 测定,评估抗生素的疗效,这些菌株是从 NSTI 患者中分离出来的。通过细胞单层感染的微量量热代谢评估,还评估了抗生素的作用,该评估提供了随时间的连续测量。辅助利福平导致在器官型皮肤组织模型中清除细菌的抗生素疗效增强,97.5%对 93.9%( = 0.006)。通过微量量热测量,辅助利福平导致所有测试的临床 GAS 菌株的代谢活性降低和迟滞期延长( < 0.05)。此外,还报告了在 GAS 组织感染持续存在的 NSTI 病例中辅助利福平治疗的病例报告。本研究的结果表明,辅助利福平可增强 GAS 生物膜在组织感染模型中的清除。

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Necrotizing skin and soft-tissue infections in the intensive care unit.重症监护病房中的皮肤和软组织坏死性感染。
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