Dehò G, Ghisotti D, Alano P, Zangrossi S, Borrello M G, Sironi G
J Mol Biol. 1984 Sep 15;178(2):191-207. doi: 10.1016/0022-2836(84)90139-6.
The satellite bacteriophage P4, in the presence of a helper phage, can enter either the lytic or the lysogenic cycle. In the absence of the helper, P4 can integrate in the bacterial chromosome. In addition, the partially immunity-insensitive mutant P4 vir1 can be maintained as a plasmid. We have found that in the absence of the helper, P4 wt also can be maintained as a plasmid, and that both P4 wt and P4 vir1 have two options for their intracellular propagation: a repressed-integrated or a derepressed-high copy number plasmid mode of maintenance. In the repressed mode, the P4 wt genome is only found integrated into the bacterial chromosome, while the P4 vir1 is found also as a low copy number plasmid coexisting with the integrated P4 vir1 genome. The clones carrying P4 in the derepressed-high copy number plasmid state are obtained at low frequency (0.3%) upon infection with P4 wt, while the vir1 mutation increases this frequency about 300-fold. Such clones can be distinguished easily because of their typical colony morphology (rosettes), due to the presence of filamentous cells. Filamentation of the bacterial host suggests that the presence of derepressed P4 genomes in high copy number interferes with the normal cell division mechanism. The derepressed clones are rather stable, but may revert spontaneously to the repressed state. Spontaneous transition from the repressed to the derepressed state was not observed; however, it can be induced by P2 or P4 vir1 superinfection of P4 wt and P4 vir1 lysogens or by growing the P4 vir1 lysogens up to the late exponential phase. The ability of P4 to choose either of two stable states and the potential to shift between these two modes of propagation indicate that the synthesis of the immunity repressor is regulated.
卫星噬菌体P4在辅助噬菌体存在的情况下,可进入裂解周期或溶原周期。在没有辅助噬菌体时,P4可整合到细菌染色体中。此外,部分免疫不敏感突变体P4 vir1可作为质粒维持。我们发现,在没有辅助噬菌体时,P4野生型也可作为质粒维持,并且P4野生型和P4 vir1在细胞内增殖都有两种选择:抑制整合或去抑制高拷贝数质粒维持模式。在抑制模式下,仅发现P4野生型基因组整合到细菌染色体中,而P4 vir1还以低拷贝数质粒的形式与整合的P4 vir1基因组共存。用P4野生型感染后,以低频率(0.3%)获得处于去抑制高拷贝数质粒状态携带P4的克隆,而vir1突变使该频率增加约300倍。由于存在丝状细胞,这些克隆因其典型的菌落形态(玫瑰花结)而易于区分。细菌宿主的丝状化表明高拷贝数的去抑制P4基因组的存在干扰了正常的细胞分裂机制。去抑制克隆相当稳定,但可能自发回复到抑制状态。未观察到从抑制状态到去抑制状态的自发转变;然而,可以通过P2或P4 vir1对P4野生型和P4 vir1溶原菌的超感染,或通过将P4 vir1溶原菌培养至指数后期来诱导。P4选择两种稳定状态之一的能力以及在这两种增殖模式之间转换的潜力表明免疫阻遏物的合成是受调控的。