Teo Jeanette W P, Tan Theresa M C, Poh Chit Laa
Programme in Environmental Microbiology, Department of Microbiology, Faculty of Medicine, National University of Singapore, Singapore.
Antimicrob Agents Chemother. 2002 Apr;46(4):1038-45. doi: 10.1128/AAC.46.4.1038-1045.2002.
Isolates of Vibrio harveyi, a prawn pathogen, have demonstrated multiple antibiotic resistance to commonly used antimicrobial agents, such as oxytetracycline. In this paper, we describe the cloning and characterization of two tetracycline resistance determinants from V. harveyi strain M3.4L. The first resistance determinant, cloned as a 4,590-bp fragment, was identical to tetA and flanking sequences encoded on transposon Tn10 from Shigella flexneri. The second determinant, cloned as a 3,358-bp fragment in pATJ1, contains two open reading frames, designated tet35 and txr. tet35 encodes a 369-amino-acid protein that was predicted to have nine transmembrane regions. It is a novel protein which has no homology to any other drug resistance protein but has low levels of homology (28%) to Na(+)/H(+) antiporters. Transposon mutagenesis showed that tet35 and txr were required for tetracycline resistance in a heterologous Escherichia coli host. Tetracycline accumulation studies indicate that E. coli carrying tet35 and txr can function as an energy-dependent tetracycline efflux pump but is less efficient than TetA.
对虾病原菌哈维氏弧菌的分离株已显示出对常用抗菌剂(如土霉素)具有多重抗生素抗性。在本文中,我们描述了从哈维氏弧菌菌株M3.4L中克隆和鉴定两个四环素抗性决定簇的过程。第一个抗性决定簇被克隆为一个4590 bp的片段,与弗氏志贺氏菌转座子Tn10上编码的tetA及其侧翼序列相同。第二个决定簇在pATJ1中被克隆为一个3358 bp的片段,包含两个开放阅读框,分别命名为tet35和txr。tet35编码一个369个氨基酸的蛋白质,预计有九个跨膜区域。它是一种新型蛋白质,与任何其他耐药蛋白均无同源性,但与Na(+)/H(+)反向转运蛋白有较低水平的同源性(28%)。转座子诱变表明,tet35和txr是异源大肠杆菌宿主中四环素抗性所必需的。四环素积累研究表明,携带tet35和txr的大肠杆菌可作为一种能量依赖性四环素外排泵发挥作用,但效率低于TetA。