Susceptibility of Vertilmicin to Modifications by Three Types of Recombinant Aminoglycoside-Modifying Enzymes

被引:4
|
作者
Yuan, Min [1 ,2 ]
Han, Hui [1 ,2 ]
Li, Cong-Ran [1 ,2 ]
Yang, Xin-Yi [1 ,2 ]
Li, Guo-Qing [1 ,2 ]
Cen, Shan [1 ,2 ]
Kang, Xi-Xiong [3 ]
Si, Shu-Yi [1 ,2 ]
Jiang, Jian-Dong [1 ,2 ]
You, Xue-Fu [1 ,2 ]
机构
[1] Chinese Acad Med Sci, Inst Med Biotechnol, Beijing 100050, Peoples R China
[2] Peking Union Med Coll, Beijing 100050, Peoples R China
[3] Capital Med Univ, Beijing Tiantan Hosp, Clin Lab, Beijing 100050, Peoples R China
基金
中国国家自然科学基金;
关键词
BETA-LACTAMASE; PSEUDOMONAS-AERUGINOSA; NUCLEOTIDE-SEQUENCE; ACETYLTRANSFERASE; GENE; MECHANISM; VARIANT; STRAIN;
D O I
10.1128/AAC.00300-11
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The susceptibilities of vertilmicin and seven reference aminoglycosides to modifications by six recombinant aminoglycoside-modifying enzymes, AAC(6')-Ie, APH(2")-Ia, AAC(6')-Ie-APH(2")-Ia, ANT(2")-Ia, AAC(6')-Ib, and AAC(6')-Ib-cr, were studied by coupled spectrophotometric assays in microtiter plates. In comparison to other aminoglycosides, the susceptibility of vertilmicin was 45.8- to 250.0-fold lower for AAC(6')-Ie acetylation, 39.2- to 116.7-fold lower for AAC(6')-Ie-APH(2")-Ia acetylation, and 1.8- to 7.5-fold lower for ANT(2")-Ia adenylation (except that shown by amikacin) while relatively comparable for AAC(6')-Ib acetylation, AAC(6')-Ib-cr acetylation, APH(2")-Ia phosphorylation, and AAC(6')-Ie-APH(2")-Ia phosphorylation.
引用
收藏
页码:3950 / 3953
页数:4
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