Kim Bokyung, Kim Shukho, Choi Yoon-Jung, Shin Minsang, Kim Jungmin
Department of Microbiology, School of Medicine, Kyungpook National University, Gukchaebosang-Ro 680, Jung-Gu, Daegu, 41944, Republic of Korea.
Untreatable Infectious Disease Institute, Kyungpook National University, Gukchaebosang-Ro 680, Jung-Gu, Daegu, 41944, Republic of Korea.
J Microbiol. 2024 Dec;62(12):1133-1153. doi: 10.1007/s12275-024-00180-7. Epub 2024 Dec 10.
Klebsiella pneumoniae, a Gram-negative opportunistic pathogen, is increasingly resistant to carbapenems in clinical settings. This growing problem necessitates the development of alternative antibiotics, with phage therapy being one promising option. In this study, we investigated novel phages targeting carbapenem-resistant Klebsiella pneumoniae (CRKP) and evaluated their lytic capacity against clinical isolates of CRKP. First, 23 CRKP clinical isolates were characterized using Multi-Locus Sequence Typing (MLST), carbapenemase test, string test, and capsule typing. MLST classified the 23 K. pneumoniae isolates into 10 sequence types (STs), with the capsule types divided into nine known and one unknown type. From sewage samples collected from a tertiary hospital, 38 phages were isolated. Phenotypic and genotypic characterization of these phages was performed using Random Amplification of Polymorphic DNA-PCR (RAPD-PCR), transmission electron microscopy (TEM), and whole genome sequencing (WGS) analysis. Host spectrum analysis revealed that each phage selectively lysed strains sharing the same STs as their hosts, indicating ST-specific activity. These phages were subtyped based on their host spectrum and RAPD-PCR, identifying nine and five groups, respectively. Fourteen phages were selected for further analysis using TEM and WGS, revealing 13 Myoviruses and one Podovirus. Genomic analysis grouped the phages into three clusters: one closely related to Alcyoneusvirus, one to Autographiviridae, and others to Straboviridae. Our results showed that the host spectrum of K. pneumoniae-specific phages corresponds to the STs of the host strain. These 14 novel phages also hold promise as valuable resources for phage therapy against CRKP.
肺炎克雷伯菌是一种革兰氏阴性机会致病菌,在临床环境中对碳青霉烯类药物的耐药性日益增强。这一日益严重的问题使得开发替代抗生素成为必要,噬菌体疗法是一个有前景的选择。在本研究中,我们调查了针对耐碳青霉烯类肺炎克雷伯菌(CRKP)的新型噬菌体,并评估了它们对CRKP临床分离株的裂解能力。首先,使用多位点序列分型(MLST)、碳青霉烯酶检测、拉丝试验和荚膜分型对23株CRKP临床分离株进行了特征分析。MLST将23株肺炎克雷伯菌分离株分为10个序列类型(STs),荚膜类型分为9种已知类型和1种未知类型。从一家三级医院采集的污水样本中分离出38株噬菌体。使用随机扩增多态性DNA-PCR(RAPD-PCR)、透射电子显微镜(TEM)和全基因组测序(WGS)分析对这些噬菌体进行了表型和基因型特征分析。宿主谱分析表明,每种噬菌体选择性地裂解与其宿主具有相同STs的菌株,表明具有ST特异性活性。根据宿主谱和RAPD-PCR对这些噬菌体进行了亚型分类,分别确定了9个和5个组。选择14株噬菌体进行进一步的TEM和WGS分析,结果显示有13株肌尾噬菌体和1株短尾噬菌体。基因组分析将这些噬菌体分为三个簇:一个与阿尔库俄纽斯病毒密切相关,一个与自复制病毒科密切相关, 其他与斯特拉病毒科密切相关。我们的结果表明,肺炎克雷伯菌特异性噬菌体的宿主谱与宿主菌株的STs相对应。这14种新型噬菌体也有望成为抗CRKP噬菌体疗法的宝贵资源。