School of Molecular Bioscience, The University of Sydney, Sydney, Australia.
Microb Drug Resist. 2011 Sep;17(3):339-43. doi: 10.1089/mdr.2010.0196. Epub 2011 Apr 8.
The aim of this study was to examine the relationship between the IncP-1α plasmid RP1 (representing RP4, RK2, R68, and R18) and two plasmids, R1033 and R934, that are known to be related to RP1. The region containing most of the antibiotic resistance genes in R1033 and R934 was mapped using polymerase chain reaction and sequenced. Both plasmids contained a copy of the class II transposon Tn1, but it was located at different sites between the position of Tn1 and the tet(A) determinant in RP1. Thus, Tn1 and the ampicillin resistance gene contained in it were acquired by the IncP1-α backbone on three separate occasions. In R1033, Tn1696 is located nearby, between Tn1 and the tet(A) determinant, and an IS186 insertion sequence was also found in this region. In R934, a defective class II transposon carrying a partial mercuric ion resistance (mer) module was found within the Tn1. These findings show that R1033 is not derived directly from RP1/RP4, refining the evolutionary pathways previously predicted for the IncP-1α plasmid family.
本研究旨在探讨 IncP-1α 质粒 RP1(代表 RP4、RK2、R68 和 R18)与两个已知与 RP1 相关的质粒 R1033 和 R934 之间的关系。使用聚合酶链反应(PCR)对 R1033 和 R934 中大多数抗生素抗性基因所在的区域进行了作图,并对其进行了测序。这两个质粒都含有一个 II 类转座子 Tn1 的拷贝,但它位于 RP1 中 Tn1 和 tet(A)决定簇的位置之间的不同位置。因此,Tn1 及其包含的氨苄青霉素抗性基因是 IncP1-α 骨架在三个不同的场合获得的。在 R1033 中,Tn1696 位于 Tn1 和 tet(A)决定簇之间的附近,并且在该区域还发现了一个 IS186 插入序列。在 R934 中,在 Tn1 内发现了一个携带部分汞离子抗性(mer)模块的缺陷 II 类转座子。这些发现表明 R1033 并非直接源自 RP1/RP4,从而完善了先前预测的 IncP-1α 质粒家族的进化途径。