Rajakumar K, Bulach D, Davies J, Ambrose L, Sasakawa C, Adler B
Department of Microbiology, Monash University, Clayton, Victoria, Australia.
Plasmid. 1997;37(3):159-68. doi: 10.1006/plas.1997.1280.
The ampicillin resistance gene from Shigella flexneri 2a strain YSH6000 was cloned and shown by Southern hybridization analysis to be closely linked to the previously cloned streptomycin, chloramphenicol, and tetracycline resistance determinants, which are borne on a chromosomally integrated 99-kb element. Analysis of this chromosomal multi-antibiotic resistance locus revealed that it had a high level of sequence and organizational similarity to an equivalent region of the Shigella R-plasmid, NR1. However, the chromosomal locus exhibited several differences, including the presence of two stretches of sequence derived from IS elements, the precise insertion of a beta-lactamase encoding oxal cassette into the Tn21-borne integron In2, a possible 17.5-kb deletion, and the loss or inactivation of the mercury resistance determinant. Based on these data, it is proposed that the chromosomal locus arose following integration of an NR1-like plasmid.
对福氏志贺菌2a菌株YSH6000的氨苄青霉素抗性基因进行了克隆,并通过Southern杂交分析表明,该基因与先前克隆的链霉素、氯霉素和四环素抗性决定簇紧密连锁,这些抗性决定簇位于一个染色体整合的99 kb元件上。对这个染色体多抗生素抗性位点的分析表明,它与志贺菌R质粒NR1的等效区域具有高度的序列和组织相似性。然而,该染色体位点存在一些差异,包括存在两段源自IS元件的序列、β-内酰胺酶编码草酸盒精确插入Tn21携带的整合子In2、可能的17.5 kb缺失以及汞抗性决定簇的缺失或失活。基于这些数据,推测该染色体位点是在一个类似NR1的质粒整合后产生的。