Liu Jiahui, Keelan Paula, Bennett Peter M, Enne Virve I
Department of Cellular and Molecular Medicine, Bristol Centre for Antimicrobial Research, University of Bristol, University Walk, Bristol, UK.
J Antimicrob Chemother. 2009 Mar;63(3):423-6. doi: 10.1093/jac/dkn523. Epub 2009 Jan 8.
The aim of this study was to characterize a putative novel macrolide efflux gene located in the vicinity of sul3 in porcine Escherichia coli.
Five sul3-encoding E. coli isolates of porcine origin were investigated by plasmid characterization and random amplification of polymorphic DNA (RAPD) PCR. Unknown DNA adjacent to the sul3 genes was amplified using a PCR approach, followed by sequencing of the fragments. The putative macrolide efflux gene was cloned into pK18. The cloned gene was characterized by susceptibility testing by Etest in the presence and absence of efflux inhibitors.
Five sul3-encoding isolates, demonstrated to be unrelated by RAPD PCR, were characterized. The immediate genetic context of sul3 in five isolates was identical to that in plasmid pVP440, and in all cases, sul3 was associated with class 1 integrons. In three isolates, an open reading frame (orf2) encoding a putative protein with 38% amino acid identity to Mef(A) was found, while the two remaining isolates contained a fragment of orf2 truncated by IS26 insertion. In three of the isolates, this DNA region was demonstrated to be located on non-conjugative plasmids. When the complete orf2 was cloned, it conferred high-level resistance to erythromycin and azithromycin, and the resistance property could be partially inhibited using the efflux inhibitor Phe-Arg beta-naphthylamide dihydrochloride. The gene was named mef(B).
A new macrolide efflux protein, Mef(B), with 38% amino acid identity to Mef(A), has been characterized and represents the second member of the mef family of genes.
本研究旨在鉴定猪源大肠杆菌中位于sul3附近的一个假定的新型大环内酯外排基因。
通过质粒鉴定和随机扩增多态性DNA(RAPD)PCR对5株猪源携带sul3的大肠杆菌分离株进行研究。使用PCR方法扩增sul3基因附近的未知DNA,随后对片段进行测序。将假定的大环内酯外排基因克隆到pK18中。通过在有和没有外排抑制剂的情况下用Etest进行药敏试验来鉴定克隆的基因。
对5株携带sul3的分离株进行了鉴定,RAPD PCR显示它们之间没有亲缘关系。5株分离株中sul3的直接遗传背景与质粒pVP440中的相同,在所有情况下,sul3都与1类整合子相关。在3株分离株中,发现了一个开放阅读框(orf2),其编码的假定蛋白与Mef(A)的氨基酸同一性为38%,而其余2株分离株含有因IS26插入而截短的orf2片段。在其中3株分离株中,该DNA区域位于非接合质粒上。当完整的orf2被克隆时,它赋予了对红霉素和阿奇霉素的高水平抗性,并且使用外排抑制剂盐酸苯丙氨酸-精氨酸β-萘酰胺可以部分抑制这种抗性。该基因被命名为mef(B)。
已鉴定出一种新的大环内酯外排蛋白Mef(B),其与Mef(A)的氨基酸同一性为38%,它是mef基因家族的第二个成员。