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Evaluation of the Efficacy of a Bacteriophage in the Treatment of Pneumonia Induced by Multidrug Resistance Klebsiella pneumoniae in Mice

机译:噬菌体治疗多药耐药性肺炎克雷伯菌引起的肺炎的疗效评价

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摘要

Multidrug-resistant Klebsiella pneumoniae (MRKP) has steadily grown beyond antibiotic control. However, a bacteriophage is considered to be a potential antibiotic alternative for treating bacterial infections. In this study, a lytic bacteriophage, phage 1513, was isolated using a clinical MRKP isolate KP 1513 as the host and was characterized. It produced a clear plaque with a halo and was classified as Siphoviridae. It had a short latent period of 30 min, a burst size of 264 and could inhibit KP 1513 growth in vitro with a dose-dependent pattern. Intranasal administration of a single dose of 2 × 109 PFU/mouse 2 h after KP 1513 inoculation was able to protect mice against lethal pneumonia. In a sublethal pneumonia model, phage-treated mice exhibited a lower level of K. pneumoniae burden in the lungs as compared to the untreated control. These mice lost less body weight and exhibited lower levels of inflammatory cytokines in their lungs. Lung lesion conditions were obviously improved by phage therapy. Therefore, phage 1513 has a great effect in vitro and in vivo, which has potential to be used as an alternative to an antibiotic treatment of pneumonia that is caused by the multidrug-resistant K. pneumoniae.
机译:耐多药肺炎克雷伯菌已经稳步发展,超出了抗生素的控制范围。但是,噬菌体被认为是治疗细菌感染的潜在抗生素替代品。在这项研究中,使用临床MRKP分离株KP 1513作为宿主,分离了溶菌性噬菌体1513,并对其进行了表征。它产生了带有光环的透明斑块,被分类为Siphoviridae。它具有30分钟的短潜伏期,爆发大小为264,并且可以在体外以剂量依赖的方式抑制KP 1513的生长。接种KP 1513后2 h鼻内给予2×10 9 PFU /小鼠单次剂量,可以保护小鼠免于致命的肺炎。在亚致死性肺炎模型中,与未治疗的对照组相比,经噬菌体治疗的小鼠在肺部表现出较低的肺炎克雷伯菌负荷水平。这些小鼠体重减轻,肺部炎症细胞因子水平降低。噬菌体疗法可明显改善肺部病变状况。因此,噬菌体1513在体外和体内均具有很大的作用,它有潜力被用作由多药耐药的肺炎克雷伯菌引起的抗生素治疗肺炎的替代方法。

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