Brnáková Z, Farkasovská J, Godány A
Institute of Molecular Biology, Centre of Excellence for Molecular Medicine, Slovak Academy of Sciences, Bratislava, Slovakia.
Folia Microbiol (Praha). 2005;50(3):187-94. doi: 10.1007/BF02931564.
Temperate bacteriophages were induced in and released from isolates of Staphylococcus aureus and Streptococcus agalactiae using mitomycin C. Various specific indicator cultures were tested for providing clear plaques after phage infection. Specific lytic mixture of bacteriophages was prepared using the induced, modified and laboratory variants of phages. Under laboratory conditions, the mixture eliminated all isolates from the tested collection of microorganisms. The restriction barrier of some bacterial isolates to bacteriophage infection was overcome either by UV irradiation or in vitro modification of bacteriophage DNA with specific methyltransferases. Conjugative R plasmids, capable of replication in G+ and G- bacteria, were detected and isolated from S. aureus and S. agalactiae antibiotic-resistant strains.
使用丝裂霉素C在金黄色葡萄球菌和无乳链球菌的分离株中诱导并释放温和噬菌体。测试了各种特定指示培养物,以确定噬菌体感染后能否产生清晰的噬菌斑。使用诱导型、修饰型和实验室型噬菌体变体制备噬菌体的特异性裂解混合物。在实验室条件下,该混合物消除了测试微生物集合中的所有分离株。通过紫外线照射或用特定甲基转移酶对噬菌体DNA进行体外修饰,克服了一些细菌分离株对噬菌体感染的限制屏障。从金黄色葡萄球菌和无乳链球菌的耐抗生素菌株中检测并分离出了能够在革兰氏阳性菌和革兰氏阴性菌中复制的接合性R质粒。