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新型噬菌体溶菌酶 LysSS 对鲍曼不动杆菌和铜绿假单胞菌的抗菌活性。

Antimicrobial activity of LysSS, a novel phage endolysin, against Acinetobacter baumannii and Pseudomonas aeruginosa.

机构信息

Department of Microbiology, School of Medicine, Kyungpook National University, 680 Gukchaebosang-ro, Jung-gu, Daegu 41944, Republic of Korea.

Department of Microbiology, School of Medicine, Kyungpook National University, 680 Gukchaebosang-ro, Jung-gu, Daegu 41944, Republic of Korea.

出版信息

J Glob Antimicrob Resist. 2020 Sep;22:32-39. doi: 10.1016/j.jgar.2020.01.005. Epub 2020 Jan 30.

Abstract

OBJECTIVES

Multidrug-resistant (MDR) bacteria are a major public-health concern. Bacteriophage endolysins (lysins) can be used as novel antimicrobial agents against bacterial infections. In this study, a novel endolysin (LysSS) containing a lysozyme-like domain was evaluated for its antibacterial activity against various species of bacteria.

METHODS

The LysSS-encoding gene was analyzed and cloned and the LysSS recombinant protein was expressed and purified. Purified LysSS was used to determine its antimicrobial activity against various bacterial species in vitro and to measure its protection rate against Acinetobacter baumannii systemic infection in an in vivo murine model.

RESULTS

Recombinant LysSS showed activity against MDR A. baumannii, MDR Escherichia coli, MDR Klebsiella pneumoniae, MDR Pseudomonas aeruginosa and Salmonella sp. without pre-treatment with an outer membrane permeabiliser. Moreover, LysSS inhibited the growth of methicillin-resistant Staphylococcus aureus (MRSA). The minimum inhibitory concentration (MIC) of LysSS against 16 MDR A. baumannii strains ranged from 0.063-0.25mg/mL. LysSS had no cytotoxic effect on A549 human lung cells below 250μg/mL. In an animal model, mice infected with A. baumannii were protected (40% survival rate with 125μg LysSS) by intraperitoneal injection of LysSS.

CONCLUSION

The current results demonstrate that LysSS may be a novel and promising antimicrobial agent against MRSA and MDR Gram-negative bacteria, including A. baumannii and P. aeruginosa.

摘要

目的

多药耐药(MDR)细菌是一个主要的公共卫生关注点。噬菌体溶菌素(裂解酶)可用作针对细菌感染的新型抗菌剂。在本研究中,评估了一种新型含有溶菌酶样结构域的内溶素(LysSS)对各种细菌的抗菌活性。

方法

分析和克隆 LysSS 编码基因,并表达和纯化 LysSS 重组蛋白。纯化的 LysSS 用于测定其对各种细菌的体外抗菌活性,并在体内小鼠模型中测定其对鲍曼不动杆菌全身感染的保护率。

结果

重组 LysSS 对未经外膜通透剂预处理的多药耐药鲍曼不动杆菌、多药耐药大肠杆菌、多药耐药肺炎克雷伯菌、多药耐药铜绿假单胞菌和沙门氏菌均具有活性。此外,LysSS 抑制耐甲氧西林金黄色葡萄球菌(MRSA)的生长。LysSS 对 16 株多药耐药鲍曼不动杆菌的最小抑菌浓度(MIC)范围为 0.063-0.25mg/mL。LysSS 在低于 250μg/mL 时对 A549 人肺细胞没有细胞毒性作用。在动物模型中,用 LysSS 腹腔注射感染鲍曼不动杆菌的小鼠得到保护(125μg LysSS 时 40%的存活率)。

结论

目前的结果表明,LysSS 可能是一种新型有前途的抗 MRSA 和多药耐药革兰氏阴性细菌(包括鲍曼不动杆菌和铜绿假单胞菌)的抗菌剂。

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