Brenot A, Werts C, Ottone C, Sertour N, Charon N W, Postic D, Baranton G, Saint Girons I
Unité de Bactériologie Moléculaire et Médicale, Institut Pasteur, Paris, France.
FEMS Microbiol Lett. 2001 Jul 24;201(2):139-43. doi: 10.1111/j.1574-6968.2001.tb10747.x.
The LE1 leptophage exhibited a host range restricted to the saprophytic Leptospira biflexa [Saint Girons et al., Res. Microbiol. 141 (1990) 1131-1133] and mainly to the Patoc 1 strain (hereafter called PFRA) kept in the Paris, France collection. Results of titration of LE1 lysates indicated the presence of a host-controlled modification and restriction system within PUSA (Patoc 1 strain maintained in the Morgantown, WV, USA collection) that was absent in PFRA. Because genomic DNA of PITAL (Patoc 1 strain maintained in Trieste, Italy) appeared smeared in pulsed field gel electrophoresis (PFGE), this strain is likely to contain nucleases that are activated upon DNA isolation. Moreover, comparative NotI digestions of PUSA and PFRA DNAs, as visualized by PFGE, indicated that PUSA belonged to a different serovar than PFRA. Finally, 16S ribosomal sequence analysis indicated that PUSA belonged to the saprophytic Leptospira meyeri species, while PITAL and PFRA appertained to L. biflexa. The evolutionary significance and the importance of the restriction and modification enzymes or non-specific nucleases within strains for genetic experiments are discussed.
LE1溶菌噬菌体表现出宿主范围局限于腐生型双曲钩端螺旋体[圣吉龙等人,《微生物学研究》141(1990)1131 - 1133],且主要针对保存在法国巴黎菌种保藏中心的帕托克1菌株(以下简称PFRA)。LE1裂解物的滴定结果表明,在美国西弗吉尼亚州摩根敦菌种保藏中心保存的PUSA(帕托克1菌株)中存在宿主控制的修饰和限制系统,而PFRA中不存在该系统。由于在脉冲场凝胶电泳(PFGE)中,意大利的里雅斯特保存的PITAL(帕托克1菌株)的基因组DNA出现拖尾现象,该菌株可能含有在DNA分离时被激活的核酸酶。此外,通过PFGE观察到的PUSA和PFRA DNA的NotI酶切比较表明,PUSA与PFRA属于不同的血清型。最后,16S核糖体序列分析表明,PUSA属于腐生型迈耶钩端螺旋体物种,而PITAL和PFRA属于双曲钩端螺旋体。本文讨论了这些菌株中的限制修饰酶或非特异性核酸酶在遗传实验中的进化意义和重要性。