State Key Laboratory of Agricultural Microbiology, College of Biomedicine and Health, College of Food Science and Technology, Huazhong Agricultural University, Wuhan, Hubei, China.
Laboratory of Bacterial Pathogenesis and Immunology, The Rockefeller University, New York, New York, USA.
Antimicrob Agents Chemother. 2023 May 17;67(5):e0151922. doi: 10.1128/aac.01519-22. Epub 2023 Apr 26.
Klebsiella pneumoniae and Pseudomonas aeruginosa are two leading causes of burn and wound infections, pneumonia, urinary tract infections, and more severe invasive diseases, which are often multidrug resistant (MDR) or extensively drug resistant. Due to this, it is critical to discover alternative antimicrobials, such as bacteriophage lysins, against these pathogens. Unfortunately, most lysins that target Gram-negative bacteria require additional modifications or outer membrane permeabilizing agents to be bactericidal. We identified four putative lysins through bioinformatic analysis of Pseudomonas and Klebsiella phage genomes in the NCBI database and then expressed and tested their intrinsic lytic activity . The most active lysin, PlyKp104, exhibited >5-log killing against K. pneumoniae, P. aeruginosa, and other Gram-negative representatives of the multidrug-resistant ESKAPE pathogens (Enterococcus faecium, Staphylococcus aureus, K. pneumonia, Acinetobacter baumannii, P. aeruginosa, and Enterobacter species) without further modification. PlyKp104 displayed rapid killing and high activity over a wide pH range and in high concentrations of salt and urea. Additionally, pulmonary surfactants and low concentrations of human serum did not inhibit PlyKp104 activity . PlyKp104 also significantly reduced drug-resistant K. pneumoniae >2 logs in a murine skin infection model after one treatment of the wound, suggesting that this lysin could be used as a topical antimicrobial against K. pneumoniae and other MDR Gram-negative infections.
肺炎克雷伯菌和铜绿假单胞菌是烧伤和伤口感染、肺炎、尿路感染和更严重的侵袭性疾病的两个主要原因,这些感染通常是多药耐药(MDR)或广泛耐药的。因此,发现针对这些病原体的替代抗菌药物(如噬菌体裂解酶)至关重要。不幸的是,大多数针对革兰氏阴性菌的裂解酶需要额外的修饰或外膜通透剂才能具有杀菌作用。我们通过对 NCBI 数据库中假单胞菌和肺炎克雷伯菌噬菌体基因组进行生物信息学分析,鉴定了四个推定的裂解酶,然后表达并测试了它们的固有裂解活性。最活跃的裂解酶 PlyKp104 对肺炎克雷伯菌、铜绿假单胞菌和其他多药耐药 ESKAPE 病原体(粪肠球菌、金黄色葡萄球菌、肺炎克雷伯菌、鲍曼不动杆菌、铜绿假单胞菌和肠杆菌属)的杀菌活性超过 5 个对数级,无需进一步修饰。PlyKp104 在广泛的 pH 范围和高盐和尿素浓度下表现出快速杀菌和高活性。此外,肺表面活性剂和低浓度的人血清不会抑制 PlyKp104 的活性。PlyKp104 还在一次治疗伤口后,显著减少了耐药性肺炎克雷伯菌>2 个对数级,这表明该裂解酶可作为一种针对肺炎克雷伯菌和其他 MDR 革兰氏阴性感染的局部抗菌药物。