Levy S B, Buu-Hoi A, Marshall B
J Bacteriol. 1984 Oct;160(1):87-94. doi: 10.1128/jb.160.1.87-94.1984.
Tetracycline resistance (Tcr) determinants from three different strains of Haemophilus parainfluenzae expressed 10-fold higher levels of resistance when mated into Escherichia coli. No plasmid was found in any of the E. coli recipients, even in matings in which a plasmid was identified in the donor Haemophilus sp. The Tcr determinant from Haemophilus sp. caused instability of resident plasmids in the recipient E. coli: all plasmids were lost within 30 generations in antibiotic-free media. However, by serial subculture in antibiotics, stable resident plasmids were obtained which carried the Tcr determinant from Haemophilus sp. and were transferable by conjugation and transformation among E. coli strains. All Haemophilus determinants hybridized with a probe for the Tcr determinant on Tn10, which bears inducible Tcr. However, Haemophilus determinants were constitutively resistant to tetracycline in the Haemophilus donors and in the E. coli recipients. This constitutive expression was recessive to wild-type Tn10 in the same cell, indicating that the constitutive phenotype resulted from the absence of an active repressor. Restrictive enzyme analysis of various E. coli plasmid derivatives bearing a Tcr determinant from Haemophilus sp. demonstrated that the inserted DNA was of similar size (8.95 to 9.35 kilobases), close to that of Tn10. Heteroduplex analysis and DNA:DNA hybridization confirmed that the Tcr determinant from Haemophilus sp. had greater than 90% homology with the Tn10 determinant, including the DNA sequence for the repressor.
来自三种不同副流感嗜血杆菌菌株的四环素抗性(Tcr)决定簇在与大肠杆菌接合时表达出的抗性水平高出10倍。在任何大肠杆菌受体中均未发现质粒,即使在供体嗜血杆菌属中鉴定出质粒的接合实验中也是如此。来自嗜血杆菌属的Tcr决定簇导致受体大肠杆菌中驻留质粒不稳定:在无抗生素培养基中,所有质粒在30代内都会丢失。然而,通过在抗生素中连续传代培养,获得了稳定的驻留质粒,这些质粒携带来自嗜血杆菌属的Tcr决定簇,并且可通过接合和转化在大肠杆菌菌株之间转移。所有嗜血杆菌决定簇都与Tn10上的Tcr决定簇探针杂交,Tn10带有可诱导的Tcr。然而,嗜血杆菌决定簇在嗜血杆菌供体和大肠杆菌受体中对四环素具有组成型抗性。这种组成型表达在同一细胞中对野生型Tn10是隐性的,表明组成型表型是由于缺乏活性阻遏物所致。对携带来自嗜血杆菌属Tcr决定簇的各种大肠杆菌质粒衍生物进行限制性酶分析表明,插入的DNA大小相似(8.95至9.35千碱基),接近Tn10的大小。异源双链分析和DNA:DNA杂交证实,来自嗜血杆菌属的Tcr决定簇与Tn10决定簇具有超过90%的同源性,包括阻遏物的DNA序列。