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肺炎克雷伯菌B5055的一种T7样裂解性噬菌体的特性:一种潜在的治疗剂。

Characterization of a T7-like lytic bacteriophage of Klebsiella pneumoniae B5055: a potential therapeutic agent.

作者信息

Verma Vivek, Harjai Kusum, Chhibber Sanjay

机构信息

Department of Microbiology, Panjab University, Chandigarh, 160014, India.

出版信息

Curr Microbiol. 2009 Sep;59(3):274-81. doi: 10.1007/s00284-009-9430-y. Epub 2009 May 30.

Abstract

Characterization of bacteriophages to be used prophylactically or therapeutically is mandatory, as use of uncharacterized bacteriophages is considered as one of the major reasons of failure of phage therapy in preantibiotic era. In the present study, one lytic bacteriophage, KPO1K2, specific for Klebsiella pneumoniae B5055, with broad host range was selected for characterization. As shown by TEM, morphologically KPO1K2 possessed icosahedral head with pentagonal nature with apex to apex head diameter of about 39 nm. Presence of short noncontractile tail (10 nm) suggested its inclusion into family Podoviridae with a designation of T7-like lytic bacteriophage. The phage growth cycle with a latent period of 15 min and a burst size of approximately 140 plaque forming units per infected cell as well as a genome of 42 kbps and structural protein pattern of this bacteriophage further confirmed its T7-like characteristics. Phage was stable over a wide pH range of 4-11 and demonstrated maximum activity at 37 degrees C. After injection into mice, at 6 h, a high phage titer was seen in blood as well as in kidney and urinary bladder, though titers in kidney and urinary bladder were higher as compared to blood. Phage got cleared completely in 36 h from blood while from kidneys and urinary bladder its clearance was delayed. We propose the use of this characterized phage, KPO1K2, as a prophylactic/therapeutic agent especially for the treatment of catheter associated UTI caused by Klebsiella pneumoniae.

摘要

对用于预防或治疗的噬菌体进行特性鉴定是必不可少的,因为使用未鉴定的噬菌体被认为是噬菌体疗法在抗生素前时代失败的主要原因之一。在本研究中,选择了一种对肺炎克雷伯菌B5055具有特异性、宿主范围广泛的裂解性噬菌体KPO1K2进行特性鉴定。如透射电子显微镜所示,KPO1K2在形态上具有二十面体头部,呈五边形,顶点到顶点的头部直径约为39nm。存在短的非收缩性尾部(10nm)表明它属于短尾噬菌体科,被指定为T7样裂解性噬菌体。该噬菌体的生长周期潜伏期为15分钟,每个感染细胞的爆发量约为140个噬菌斑形成单位,以及42kbps的基因组和结构蛋白模式进一步证实了其T7样特征。噬菌体在4-11的宽pH范围内稳定,在37℃时表现出最大活性。注射到小鼠体内后,在6小时时,血液以及肾脏和膀胱中出现高噬菌体滴度,尽管肾脏和膀胱中的滴度高于血液。噬菌体在36小时内从血液中完全清除,而从肾脏和膀胱中的清除则延迟。我们建议使用这种已鉴定的噬菌体KPO1K2作为预防/治疗剂,特别是用于治疗由肺炎克雷伯菌引起的导管相关性尿路感染。

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