Kameda M, Harada K, Suzuki M, Mitsuhashi S
J Bacteriol. 1965 Nov;90(5):1174-81. doi: 10.1128/jb.90.5.1174-1181.1965.
Kameda, Mitsuo (Gunma University, Maebashi, Japan), Kenji Harada, Mitsue Suzuki, and Susumu Mitsuhashi. Drug resistance of enteric bacteria. V. High frequency of transduction of R factors with bacteriophage epsilon. J. Bacteriol. 90:1174-1181. 1965.-In the transduction of R factors with phage epsilon(15), a lysate capable of transducing the markers for (TC) or (CM.SM.SA) resistance at high frequency was obtained. The transducing agent is a defective element called epsilon(15)dR(23) which lacks certain functions of phage epsilon(15). After lysogenization with normal epsilon(15) phage and ultraviolet (UV) induction, strains carrying the epsilon(15)dR(23) element produce lysates which have a high frequency of transduction (HFT) on group E(1)Salmonella. Lytic lysates prepared on phage epsilon(15) sensitive strain with the epsilon(15)dR(23) element have a low frequency of transduction (LFT). Lytic growth of phage epsilon(34) on an epsilon(15)dR(23) strain or UV induction of an epsilon(34) lysogenic strain containing epsilon(15)dR(23) results in LFT lysates on group E(2)Salmonella. On UV induction, group E(2)Salmonella (epsilon(15) lysogens) with the epsilon(15)dR(23) element give lysates which are HFT on group E(1)Salmonella but are LFT when tested on group E(2)Salmonella. In all instances, the production of drug-resistant transductants requires infection of the cell with only a single epsilon(15)dR(23) element. It appears that the resistance region of the R factor has replaced that portion of phage genome which is essential for vegetative replication and superinfection immunity. The epsilon(15)dR(23) element does not contain the genetic determinants of the R factor responsible for transmissibility, inhibition of F mating, and interference between two R factors.
龟田光夫(日本前桥市群马大学)、原田健二、铃木光枝和三桥进。肠道细菌的耐药性。V. 用噬菌体ε高频转导R因子。《细菌学杂志》90:1174 - 1181。1965年。——在用噬菌体ε(15)转导R因子时,获得了一种能够高频转导(TC)或(CM.SM.SA)耐药性标记的裂解物。转导因子是一种称为ε(15)dR(23)的缺陷元件,它缺乏噬菌体ε(15)的某些功能。在用正常的ε(15)噬菌体进行溶源化和紫外线(UV)诱导后,携带ε(15)dR(23)元件的菌株产生的裂解物对E(1)群沙门氏菌具有高频转导(HFT)能力。用带有ε(15)dR(23)元件的噬菌体ε(15)敏感菌株制备的裂解性裂解物转导频率较低(LFT)。噬菌体ε(34)在ε(15)dR(23)菌株上的裂解生长或含有ε(15)dR(23)的ε(34)溶源菌株的紫外线诱导会产生对E(2)群沙门氏菌转导频率较低(LFT)的裂解物。经紫外线诱导后,带有ε(15)dR(23)元件的E(2)群沙门氏菌(ε(15)溶源菌)产生的裂解物对E(1)群沙门氏菌是高频转导(HFT)的,但对E(2)群沙门氏菌进行测试时是低频转导(LFT)的。在所有情况下,产生耐药转导子仅需用单个ε(15)dR(23)元件感染细胞。看来R因子的耐药区域已经取代了噬菌体基因组中对营养复制和超感染免疫至关重要的那部分。ε(15)dR(23)元件不包含负责R因子可传递性、抑制F交配以及两个R因子之间干扰的遗传决定因素。