Borecká P, Rosypal S, Pantůcek R, Doskar J
Department of Genetics and Molecular Biology, Faculty of Science, Masaryk University, Brno, Czech Republic.
FEMS Microbiol Lett. 1996 Oct 1;143(2-3):203-10. doi: 10.1111/j.1574-6968.1996.tb08481.x.
Several Staphylococcus aureus strains were lysogenized by the phages of serological group B (phages phi 53, phi 85) as well as by some of serological group F (phages phi 77, phi 84) and macrorestriction fragment patterns of genomic DNA were estimated in the lysogenized, non-lysogenic and delysogenized (cured of prophages) strains. It was shown that the integration of phage DNA into chromosome of S. aureus leads to specific changes in restriction fragment pattern in all the lysogenized strains. These changes correlate well with the SmaI restriction map of S. aureus NCTC 8325 since they concern the restriction fragments defined in this map. Phages phi 53 and phi 85 integrate into SmaI fragment B. On the other hand, phages phi 77 and phi 84 integrate into SmaI fragment E of the S. aureus restriction map. The prophages of strain NCTC 8511 have their integration sites, as follows: the phage designated by us phi M integrates in fragment A, whereas the integration site for phage phi J lies in fragment E. Phage phi M was estimated to be genetically related to phages of serological group A and phage phi J to those of serological group F. Evidence was given that lysogenization of S. aureus strains by at least four prophages does not cast any doubt upon the estimation of their genetic relatedness based on their similarity in restriction pattern.
几种金黄色葡萄球菌菌株被B血清群噬菌体(噬菌体phi 53、phi 85)以及一些F血清群噬菌体(噬菌体phi 77、phi 84)溶源化,并对溶源化、非溶源化和去溶源化(去除原噬菌体)菌株的基因组DNA的宏观限制性片段模式进行了评估。结果表明,噬菌体DNA整合到金黄色葡萄球菌染色体中会导致所有溶源化菌株的限制性片段模式发生特异性变化。这些变化与金黄色葡萄球菌NCTC 8325的SmaI限制性图谱密切相关,因为它们涉及该图谱中定义的限制性片段。噬菌体phi 53和phi 85整合到SmaI片段B中。另一方面,噬菌体phi 77和phi 84整合到金黄色葡萄球菌限制性图谱的SmaI片段E中。菌株NCTC 8511的原噬菌体有其整合位点,如下:我们命名的噬菌体phi M整合到片段A中,而噬菌体phi J的整合位点位于片段E中。估计噬菌体phi M与A血清群噬菌体有遗传关系,噬菌体phi J与F血清群噬菌体有遗传关系。有证据表明,至少四种原噬菌体对金黄色葡萄球菌菌株的溶源化并不影响基于其限制性模式相似性对其遗传相关性的评估。