Bourret R B, Fox M S
Department of Biology, Massachusetts Institute of Technology, Cambridge 02139.
J Bacteriol. 1988 Apr;170(4):1672-82. doi: 10.1128/jb.170.4.1672-1682.1988.
The possible outcomes of infection of Escherichia coli by bacteriophage Mu include lytic growth, lysogen formation, nonlysogenic surviving cells, and perhaps simple killing of the host. The influence of various parameters, including host himA and himD mutations, on lysogeny and cell survival is described. Mu does not grow lytically in or kill him bacteria but can lysogenize such hosts. Mu c+ lysogenizes about 8% of him+ bacteria infected at low multiplicity at 37 degrees C. The frequency of lysogens per infected him+ cell diminishes with increasing multiplicity of infection or with increasing temperature over the range from 30 to 42 degrees C. In him bacteria, the Mu lysogenization frequency increases from about 7% at low multiplicity of infection to approach a maximum where most but not all cells are lysogens at high multiplicity of infection. Lysogenization of him hosts by an assay phage marked with antibiotic resistance is enhanced by infection with unmarked auxiliary phage. This helping effect is possible for at least 1 h, suggesting that Mu infection results in formation of a stable intermediate. Mu immunity is not required for lysogenization of him hosts. We argue that in him bacteria, all Mu genomes which integrate into the host chromosome form lysogens.
噬菌体Mu感染大肠杆菌的可能结果包括裂解生长、溶原形成、非溶原存活细胞,也许还包括简单地杀死宿主。描述了包括宿主himA和himD突变在内的各种参数对溶原性和细胞存活的影响。Mu在him细菌中不会进行裂解生长或杀死它们,但可以使这些宿主溶原化。Mu c+在37℃以低感染复数感染时,能使约8%的him+细菌溶原化。每个被感染的him+细胞的溶原频率随着感染复数的增加或在30至42℃范围内温度的升高而降低。在him细菌中,Mu溶原化频率从低感染复数时的约7%增加,在高感染复数时接近最大值,此时大多数但不是所有细胞都是溶原菌。用带有抗生素抗性标记的检测噬菌体对him宿主进行溶原化,会因未标记的辅助噬菌体感染而增强。这种辅助作用至少可持续1小时,表明Mu感染会导致形成稳定的中间体。him宿主的溶原化不需要Mu免疫。我们认为,在him细菌中,所有整合到宿主染色体中的Mu基因组都会形成溶原菌。