Werckenthin C, Schwarz S, Roberts M C
Institut für Kleintierforschung Celle/Merbitz der Bundesforschungsanstalt für Landwirtschaft Braunschweig-Völkenrode, Celle, Germany.
Antimicrob Agents Chemother. 1996 Nov;40(11):2542-4. doi: 10.1128/AAC.40.11.2542.
Four large staphylococcal plasmids ranging in size from 31 to 82 kbp have been shown to mediate tetracycline resistance via an integrated copy of the tet(K)-encoding plasmid pT181 which was flanked by copies of the insertion element IS257. In two cases, IS257 elements interrupted the repC reading frame of pT181 and an 8-bp sequence from within the repC gene was duplicated at the interrupted site. In the third plasmid, the IS257 elements interrupted the pT181 DNA immediately upstream of the repC coding sequence with an 8-bp duplication. In the fourth case, the IS257 elements flanked a pT181-like plasmid with one IS257 in the repC coding sequence and the other within the recombinase (pre) coding sequence, so that a section of the pT181 sequence was deleted. All four integration sites detected in this study differ from those previously described for the IS257-mediated integration of pT181-like plasmids into large plasmids or into the chromosomal DNA.
已证实有4个大小在31至82千碱基对之间的葡萄球菌大质粒通过编码tet(K)的质粒pT181的整合拷贝介导四环素抗性,该整合拷贝两侧为插入元件IS257的拷贝。在两种情况下,IS257元件中断了pT181的repC阅读框,repC基因内的一个8碱基序列在中断位点处发生了重复。在第三个质粒中,IS257元件在repC编码序列上游紧邻处中断了pT181 DNA,并伴有一个8碱基重复。在第四种情况下,IS257元件位于一个类似pT181的质粒两侧,一个IS257在repC编码序列中,另一个在重组酶(前体)编码序列内,从而导致pT181序列的一部分缺失。本研究中检测到的所有4个整合位点均与先前描述的IS257介导的类似pT181的质粒整合到大质粒或染色体DNA中的位点不同。