Bryan L E, Semaka S D, Van den Elzen H M, Kinnear J E, Whitehouse R L
Antimicrob Agents Chemother. 1973 May;3(5):625-37. doi: 10.1128/AAC.3.5.625.
R factors were detected in 3.3% of 233 hospital isolates of Pseudomonas aeruginosa using P. aeruginosa recipients in conjugations. Transferred markers included streptomycin, tetracycline, and sulfonamide resistance. Gentamicin resistance was transferred from two strains previously shown to acetylate gentamicin. A group of R factors exemplified by R931 were characterized by failure to transfer to Escherichia coli recipients. Such R factors formed a single compatibility group when examined in a P. aeruginosa recipient. Other P. aeruginosa R factors, including RP4, showed stable coexistence with the R931 group. It is proposed that RP4 and similar R factors be members of the P-1 compatibility group and that R931, R3108, R209, and R130 be members of a group termed P-2. The buoyant densities of all R factors examined were similar, about 1.716 to 1.719 g/cm(3). The content of R-factor deoxyribonucleic acid (DNA) relative to the total DNA varied among the different R factors, ranging from about 18 +/- 2% in log-phase cells of 931 (R931) to undetectable for 679 (R679). However, R679, which transferred from strain 679 at extremely low and irregular frequencies to an E. coli host, was shown to represent about 4% R-factor DNA in that host. The relative DNA content of R931 appeared to decline in the stationary growth phase of 931 (R931) or 280 (R931). R931 covalently closed circular DNA was isolated by ethidium bromide-CsCl gradient centrifugation and examined by electron microscopy. Two major molecular distributions existed, having contour lengths of 0.5 and 12.4 mum. The molecular weights were estimated to be 10(6) and 25 x 10(6). Both molecules were under relaxed replication control. R factor R931 exists as a naturally occurring high-frequency transfer system in P. aeruginosa strains 931 and 1310. However, in strain 280 it acts as if subject to fertility repression. Other members of the P-2 compatibility group also are high-frequency transfer systems in the natural host and in strain 1310. RP4 is restricted from recipient strain 1310. Some additional recipient effects were noted in that strains 1310 or 280 sometimes differed in recipient effectiveness with a given donor. Agglutination reactions with absorbed antiserum were able to distinguish between two members of the same R-factor compatibility group, R931 and R3108.
在233株从医院分离出的铜绿假单胞菌中,利用铜绿假单胞菌作为接合受体,检测到3.3%的菌株带有R因子。转移的标记包括对链霉素、四环素和磺胺类药物的抗性。庆大霉素抗性从之前显示可使庆大霉素乙酰化的两株菌株中转移。以R931为例的一组R因子的特征是不能转移到大肠杆菌受体中。当在铜绿假单胞菌受体中检测时,这类R因子形成一个单一的相容群。其他铜绿假单胞菌R因子,包括RP4,与R931组表现出稳定共存。有人提出,RP4及类似的R因子是P - 1相容群的成员,而R931、R3108、R209和R130是一个称为P - 2组的成员。所有检测的R因子的浮力密度相似,约为1.716至1.719 g/cm³。不同R因子中R因子脱氧核糖核酸(DNA)相对于总DNA的含量各不相同,在931(R931)对数期细胞中约为18±2%,而在679(R679)中则检测不到。然而,从菌株679以极低且不规则频率转移到大肠杆菌宿主的R679,在该宿主中显示约占4%的R因子DNA。R931的相对DNA含量在931(R931)或280(R931)的稳定生长期似乎有所下降。通过溴化乙锭 - 氯化铯梯度离心分离出R931共价闭合环状DNA,并通过电子显微镜检查。存在两种主要的分子分布,其轮廓长度分别为0.5和12.4μm。分子量估计分别为10⁶和25×⁶。这两种分子都处于松弛复制控制之下。R因子R931在铜绿假单胞菌菌株931和1310中作为一种天然存在的高频转移系统存在。然而,在菌株280中,它的行为似乎受到致育性抑制。P - 2相容群的其他成员在天然宿主和菌株1310中也是高频转移系统。RP4不能转移到受体菌株1310。还注意到一些其他受体效应,即菌株1310或280有时在接受给定供体时的受体效能有所不同。用吸收后的抗血清进行的凝集反应能够区分同一R因子相容群的两个成员,即R931和R3108。