A POINT MUTATION IN NORA GENE IS RESPONSIBLE FOR QUINOLONE RESISTANCE IN STAPHYLOCOCCUS-AUREUS

被引:28
作者
OHSHITA, Y
HIRAMATSU, K
YOKOTA, T
机构
[1] Department of Microbiology, Faculty of Medicine, Juntendo University, 113, 2-1-1 Hongo, Bunkyo-ku, Tokyo, Japan
关键词
D O I
10.1016/0006-291X(90)91549-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Two norA genes associated with hydrophilic quinolone resistance in Staphylococcus aureus were identified on the two recombinant plasmids pMR8736 and pSA209; the former was derived from a quinolone-resistant strain MR8736, and the latter was derived from a fluoroquinolone-susceptible strain 209P. We compared functions of these two genes, norA8736 and norA209 respectively, by introducing them into E. coli MC1061. Both genes expressed a novel protein of 52 kilodalton (kD) in size in MC1061. However, only norA8736 could confer hydrophilic quinolone resistance to the host cell, which was accompanied by a significant decrease in the uptake of a hydrophilic quinolone, norfloxacin, by the cell. Subcloning and recombinant plasmid analyses localized the hydrophilic quinolone-resistance marker to the 0.5 kilobase (kb)-long HpaI-HinfI DNA fragment of pMR8736. Nucleotide sequencing of this region and the corresponding region of pSA209 revealed that the hydrophilic quinolone resistance conferred by norA8736 was caused by a single nucleotide substitution from A (adenosine) in norA209 to C (cytosine), which corresponded to a single amino acid substitution from Asp to Ala. © 1990.
引用
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页码:1028 / 1034
页数:7
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