Park Eun-Ah, Kim You-Tae, Cho Jae-Hyun, Ryu Sangryeol, Lee Ju-Hoon
Department of Food Science and Biotechnology, Institute of Life Sciences and Resources, Kyung Hee University, Yongin, 446-701, Korea.
Department of Food and Animal Biotechnology, Department of Agriculture Biotechnology, Research Institute of Agriculture and Life Sciences, and Center for Food and Bioconvergence, Seoul National University, Seoul, 151-921, Korea.
Arch Virol. 2017 Apr;162(4):1129-1139. doi: 10.1007/s00705-016-3202-3. Epub 2016 Dec 27.
Klebsiella is a genus of well-known opportunistic human pathogens that are associated with diabetes mellitus and chronic pulmonary obstruction; however, this pathogen is often resistant to multiple drugs. To control this pathogen, two Klebsiella-infecting phages, K. oxytoca phage PKO111 and K. pneumoniae phage PKP126, were isolated from a sewage sample. Analysis of their host range revealed that they infect K. pneumoniae and K. oxytoca, suggesting host specificity for members of the genus Klebsiella. Stability tests confirmed that the phages are stable under various temperature (4 to 60 °C) and pH (3 to 11) conditions. A challenge assay showed that PKO111 and PKP126 inhibit growth of their host strains by 2 log and 4 log, respectively. Complete genome sequencing of the phages revealed that their genome sizes are quite different (168,758 bp for PKO111 and 50,934 bp for PKP126). Their genome annotation results showed that they have no human virulence-related genes, an important safety consideration. In addition, no lysogen-formation gene cluster was detected in either phage genome, suggesting that they are both virulent phages in their bacterial hosts. Based on these results, PKO111 and PKP126 may be good candidates for development of biocontrol agents against members of the genus Klebsiella for therapeutic purposes. A comparative analysis of tail-associated gene clusters of PKO111 and PKP126 revealed relatively low homology, suggesting that they might differ in the way they recognize and infect their specific hosts.
克雷伯氏菌属是一类著名的人类机会致病菌,与糖尿病和慢性阻塞性肺病相关;然而,这种病原体常常对多种药物耐药。为了控制这种病原体,从一份污水样本中分离出了两种感染克雷伯氏菌的噬菌体,即产酸克雷伯氏菌噬菌体PKO111和肺炎克雷伯氏菌噬菌体PKP126。对它们宿主范围的分析表明,它们感染肺炎克雷伯氏菌和产酸克雷伯氏菌,提示对克雷伯氏菌属成员具有宿主特异性。稳定性测试证实,这些噬菌体在各种温度(4至60°C)和pH(3至11)条件下都很稳定。一项挑战试验表明,PKO111和PKP126分别将其宿主菌株的生长抑制了2个对数和4个对数。噬菌体的全基因组测序显示,它们的基因组大小差异很大(PKO111为168,758 bp,PKP126为50,934 bp)。它们的基因组注释结果表明,它们没有与人类毒力相关的基因,这是一个重要的安全考量。此外,在任何一个噬菌体基因组中都未检测到溶原形成基因簇,提示它们在其细菌宿主中均为烈性噬菌体。基于这些结果,PKO111和PKP126可能是开发用于治疗目的的针对克雷伯氏菌属成员的生物防治剂的良好候选者。对PKO111和PKP126的尾部相关基因簇的比较分析显示同源性相对较低,提示它们在识别和感染其特定宿主的方式上可能存在差异。