Kwoh D Y, Kemper J
J Virol. 1978 Sep;27(3):535-50. doi: 10.1128/JVI.27.3.535-550.1978.
The temperate bacteriophage P22 mediates both generalized and specialized transduction in Salmonella typhimurium. Specialized transduction by phage P22 is different from, and less restricted than, the well characterized specialized transduction by phage lambda, due to differences in the phage DNA packaging mechanism. Phage lysates produced by induction of lysogenic strains contain very high frequencies of supQ newD- and proA,B-specialized transducing particles (10(-2)/PFU and 10(-3)/PFU, respectively), most of which are produced by independent aberrant excision events of various types. In a model, 12 different modes of transduction mechanisms were characterized by: (i) the structure of the specialized transducing genomes after injection into a new host cell, i.e., linear or circular, and (ii) the requirements for the transduction process, i.e., host recombination functions, phage integration functions, or presence of a prophage. By using different recipient strains and phage helper strains, it was possible to show that most specialized transducing particles (ca. 99%) contain linear genomes that cannot circularize upon injection into a new host cell and that require the presence of an integrated prophage as a site for a recombinational event to give rise to a transductant. Only 0.1% of all specialized transducing particles were shown to transduce by integration, suggesting that transducing genomes containing terminally redundant ends represent only a minor fraction of all transducing particles that are produced. However, it should be pointed out that the frequency (approximately 10(-5)/PFU) of these specialized transducing genomes that can circularize upon injection into a new host cell is as high as or even higher than the frequency of specialized transducing particles of phage lambda. The remaining approximately 1% of all specialized transducing particles can transduce by any one of the other mechanisms described.
温和噬菌体P22介导鼠伤寒沙门氏菌的普遍性转导和特异性转导。由于噬菌体DNA包装机制的差异,噬菌体P22的特异性转导不同于且比特征明确的噬菌体λ的特异性转导限制更少。通过诱导溶源菌产生的噬菌体裂解物含有非常高频率的supQ、newD - 和proA,B特异性转导颗粒(分别为10^(-2)/PFU和10^(-3)/PFU),其中大多数是由各种类型的独立异常切除事件产生的。在一个模型中,12种不同的转导机制模式的特征如下:(i) 注入新宿主细胞后特异性转导基因组的结构,即线性或环状;(ii) 转导过程的要求,即宿主重组功能、噬菌体整合功能或原噬菌体的存在。通过使用不同的受体菌株和噬菌体辅助菌株,有可能表明大多数特异性转导颗粒(约99%)含有线性基因组,这些基因组在注入新宿主细胞后不能环化,并且需要存在整合的原噬菌体作为重组事件的位点才能产生转导子。所有特异性转导颗粒中只有0.1%被证明通过整合进行转导,这表明含有末端冗余末端的转导基因组仅占所有产生的转导颗粒的一小部分。然而,应该指出的是,这些注入新宿主细胞后能够环化的特异性转导基因组的频率(约10^(-5)/PFU)与噬菌体λ的特异性转导颗粒的频率一样高甚至更高。其余约1%的所有特异性转导颗粒可以通过所述的任何一种其他机制进行转导。