Wang Feng, Xiao Yao, Lu Yao, Deng Zheng-Yu, Deng Xian-Yu, Lin Lian-Bing
Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, China.
Engineering Research Center for Replacement Technology of Feed Antibiotics of Yunnan College, Kunming, China.
Front Microbiol. 2022 Feb 14;13:821989. doi: 10.3389/fmicb.2022.821989. eCollection 2022.
Developing new strategies to replace or supplement antibiotics to combat bacterial infection is a pressing task in the field of microbiological research. In this study, we report a lytic enzyme named P9ly deriving from the bacteriophage PSD9 that could infect multidrug-resistant . This enzyme was identified through whole-genome sequencing of PSD9. The results show that P9ly contains a conserved T4-like_lys domain and belongs to the phage lysozyme family. Recombinant P9ly obtained from protein purification presented biological activity and could digest bacterial cell walls (CW), resulting in the destruction of cell structure and leakage of intracellular components. Furthermore, P9ly exhibited bacteriolytic and bactericidal activity on different strains, especially multidrug-resistant Gram-negative and Gram-positive . Additionally, combined use of P9ly with ceftriaxone sodium (CRO) could decrease necessary dose of the antibiotic used and improve the antibacterial effect. In summary, under the current backdrop of extensive antibiotic usage and the continuous emergence of bacterial resistance, this study provides an insight into developing bacteriophage-based antibacterial agents against both Gram-negative and Gram-positive pathogens.
开发新的策略来替代或补充抗生素以对抗细菌感染是微生物研究领域的一项紧迫任务。在本研究中,我们报道了一种源自噬菌体PSD9的裂解酶P9ly,该噬菌体可感染多重耐药菌。这种酶是通过对PSD9进行全基因组测序鉴定出来的。结果表明,P9ly含有一个保守的T4样溶菌结构域,属于噬菌体溶菌酶家族。通过蛋白质纯化获得的重组P9ly具有生物活性,能够消化细菌细胞壁(CW),导致细胞结构破坏和细胞内成分泄漏。此外,P9ly对不同菌株,尤其是多重耐药革兰氏阴性菌和革兰氏阳性菌表现出溶菌和杀菌活性。此外,P9ly与头孢曲松钠(CRO)联合使用可降低抗生素的必要使用剂量并提高抗菌效果。总之,在当前抗生素广泛使用和细菌耐药性不断出现的背景下,本研究为开发针对革兰氏阴性和革兰氏阳性病原体的基于噬菌体的抗菌剂提供了思路。