Division of Infectious Diseases, University of California San Diego, La Jolla, CA 92093, USA; Infectious Diseases Section, VA San Diego Healthcare System, San Diego, CA 92161, USA.
Department of Pediatrics, University of California San Diego, La Jolla, CA 92093, USA.
Int J Antimicrob Agents. 2018 Mar;51(3):468-478. doi: 10.1016/j.ijantimicag.2017.12.032. Epub 2018 Jan 11.
Endocarditis is a rare but serious manifestation of Listeria monocytogenes (LM). However, the optimal treatment strategy for LM endocarditis has yet to be established. Current antibiotic strategies for listeriosis include penicillin G or ampicillin (AMP) monotherapy, or AMP + gentamicin combination therapy which is often favored for endocarditis. The primary objective of our investigation was to assess the utility of AMP + ceftriaxone (CRO) and AMP + daptomycin (DAP) against LM, modeling less nephrotoxic antibiotic combinations traditionally used to manage resistant enterococcal endocarditis. Here we report a case of LM endocarditis, review the world literature, and evaluate alternative treatment strategies for listeriosis utilizing in vitro and ex vivo studies. The combination of AMP + CRO and AMP + DAP were each noted to have synergistic activity against a LM endocarditis isolate. Additionally, co-incubation of the isolate with sub-lethal concentrations of antibiotics (AMP, CRO, DAP, AMP + CRO or AMP + DAP) sensitized the bacterium to whole blood killing while pretreatment with CRO and DAP (at 1/4 MIC) sensitized the bacterium to neutrophil killing. However, these effects did not reflect potentiation of antibiotic activity to human cathelicidin peptide LL-37, which is abundant in neutrophils and highly active against LM. Interestingly, AMP pretreatment of the LM endocarditis isolate resulted in increased DAP binding to the bacterium when assessed by fluorescence microscopy. These in vitro and ex vivo studies suggest further investigation of combination therapy using AMP + CRO or AMP + DAP as an alternative treatment for LM infection is warranted.
心内膜炎是李斯特菌(LM)感染的罕见但严重的表现形式。然而,LM 心内膜炎的最佳治疗策略尚未确定。李斯特菌感染的当前抗生素治疗策略包括青霉素 G 或氨苄西林(AMP)单药治疗,或 AMP+庆大霉素联合治疗,后者常用于治疗心内膜炎。我们研究的主要目的是评估 AMP+头孢曲松(CRO)和 AMP+达托霉素(DAP)对 LM 的作用,模拟传统上用于治疗耐药肠球菌心内膜炎的肾毒性较小的抗生素组合。在这里,我们报告了 1 例 LM 心内膜炎病例,回顾了世界文献,并利用体外和离体研究评估了李斯特菌感染的替代治疗策略。AMP+CRO 和 AMP+DAP 的联合使用均被证明对 LM 心内膜炎分离株具有协同作用。此外,将分离株与亚致死浓度的抗生素(AMP、CRO、DAP、AMP+CRO 或 AMP+DAP)共孵育可使细菌对全血杀伤敏感,而 CRO 和 DAP(在 1/4 MIC 下)预处理可使细菌对中性粒细胞杀伤敏感。然而,这些作用并没有反映出抗生素对人防御素肽 LL-37 的活性增强,LL-37 在中性粒细胞中含量丰富,对 LM 高度有效。有趣的是,当通过荧光显微镜评估时,AMP 预处理 LM 心内膜炎分离株可增加 DAP 与细菌的结合。这些体外和离体研究表明,需要进一步研究 AMP+CRO 或 AMP+DAP 联合治疗作为 LM 感染的替代治疗方法。