Liebert C A, Hall R M, Summers A O
Department of Microbiology, The University of Georgia, Athens, Georgia 30602-2605, USA.
Microbiol Mol Biol Rev. 1999 Sep;63(3):507-22. doi: 10.1128/MMBR.63.3.507-522.1999.
The transposon Tn21 and a group of closely related transposons (the Tn21 family) are involved in the global dissemination of antibiotic resistance determinants in gram-negative facultative bacteria. The molecular basis for their involvement is carriage by the Tn21 family of a mobile DNA element (the integron) encoding a site-specific system for the acquisition of multiple antibiotic resistance genes. The paradigm example, Tn21, also carries genes for its own transposition and a mercury resistance (mer) operon. We have compiled the entire 19,671-bp sequence of Tn21 and assessed the possible origins and functions of the genes it contains. Our assessment adds molecular detail to previous models of the evolution of Tn21 and is consistent with the insertion of the integron In2 into an ancestral Tn501-like mer transposon. Codon usage analysis indicates distinct host origins for the ancestral mer operon, the integron, and the gene cassette and two insertion sequences which lie within the integron. The sole gene of unknown function in the integron, orf5, resembles a puromycin-modifying enzyme from an antibiotic producing bacterium. A possible seventh gene in the mer operon (merE), perhaps with a role in Hg(II) transport, lies in the junction between the integron and the mer operon. Analysis of the region interrupted by insertion of the integron suggests that the putative transposition regulator, tnpM, is the C-terminal vestige of a tyrosine kinase sensor present in the ancestral mer transposon. The extensive dissemination of the Tn21 family may have resulted from the fortuitous association of a genetic element for accumulating multiple antibiotic resistances (the integron) with one conferring resistance to a toxic metal at a time when clinical, agricultural, and industrial practices were rapidly increasing the exposure to both types of selective agents. The compendium offered here will provide a reference point for ongoing observations of related elements in multiply resistant strains emerging worldwide.
转座子Tn21及一组密切相关的转座子(Tn21家族)参与革兰氏阴性兼性细菌中抗生素耐药决定因子的全球传播。其参与传播的分子基础是Tn21家族携带一个可移动DNA元件(整合子),该元件编码一个用于获取多个抗生素耐药基因的位点特异性系统。典型例子Tn21还携带自身转座基因和一个汞抗性(mer)操纵子。我们已汇编了Tn21完整的19671 bp序列,并评估了其所含基因的可能起源和功能。我们的评估为之前的Tn21进化模型增添了分子细节,并且与整合子In2插入到一个祖先类Tn501的mer转座子中相一致。密码子使用分析表明,祖先mer操纵子、整合子、基因盒以及整合子内的两个插入序列有不同的宿主起源。整合子中唯一功能未知的基因orf5类似于一种来自抗生素产生菌的嘌呤霉素修饰酶。mer操纵子中可能的第七个基因(merE)或许在Hg(II)转运中起作用,它位于整合子和mer操纵子的交界处。对整合子插入中断区域的分析表明,推定的转座调节因子tnpM是祖先mer转座子中存在的酪氨酸激酶传感器的C端残余。Tn21家族的广泛传播可能是由于在临床、农业和工业实践迅速增加对这两种选择剂暴露的时候,一个积累多种抗生素抗性的遗传元件(整合子)与一个赋予对有毒金属抗性的元件偶然结合所致。这里提供的综述将为持续观察全球出现的多重耐药菌株中的相关元件提供一个参考点。