溶解循环
肌病毒科
微生物学
铜绿假单胞菌
噬菌体
生物
毒力
整合酶
背景(考古学)
噬菌体疗法
细菌
抗生素
多重耐药
抗生素耐药性
基因组
病毒学
基因
病毒
遗传学
大肠杆菌
人类免疫缺陷病毒(HIV)
古生物学
作者
Liliam K. Harada,Erica C. Silva,Fernando Rossi,Basilio Cieza,Thais Jardim Oliveira,Carla Pereira,Geizecler Tomazetto,Bianca G. Belline,Fábio M. Squina,Marta Maria Duarte Carvalho Vila,João Carlos Setúbal,Taekjip Ha,da Silva,Victor M. Balcão
出处
期刊:Future Microbiology
[Future Medicine]
日期:2022-01-01
卷期号:17 (2): 111-141
被引量:6
标识
DOI:10.2217/fmb-2021-0027
摘要
Aim: Two lytic phages were isolated using P. aeruginosa DSM19880 as host and fully characterized. Materials & methods: Phages were characterized physicochemically, biologically and genomically. Results & conclusion: Host range analysis revealed that the phages also infect some multidrug-resistant (MDR) P. aeruginosa clinical isolates. Increasing MOI from 1 to 1000 significantly increased phage efficiency and retarded bacteria regrowth, but phage ph0034 (reduction of 7.5 log CFU/ml) was more effective than phage ph0031 (reduction of 5.1 log CFU/ml) after 24 h. Both phages belong to Myoviridae family. Genome sequencing of phages ph0031 and ph0034 showed that they do not carry toxin, virulence, antibiotic resistance and integrase genes. The results obtained are highly relevant in the actual context of bacterial resistance to antibiotics.
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