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葡萄球菌属和肠球菌属中对杀菌性DNA聚合酶抑制剂N(3)-羟丁基6-(3'-乙基-4'-甲基苯胺基)尿嘧啶耐药的频率较低。

Low frequencies of resistance among Staphylococcus and Enterococcus species to the bactericidal DNA polymerase inhibitor N(3)-hydroxybutyl 6-(3'-ethyl-4'-methylanilino) uracil.

作者信息

Butler Michelle M, Skow Donna J, Stephenson Ryan O, Lyden Patrick T, LaMarr William A, Foster Kimberly A

机构信息

Microbiotix, Inc., Worcester, Massachusetts 01605, USA.

出版信息

Antimicrob Agents Chemother. 2002 Dec;46(12):3770-5. doi: 10.1128/AAC.46.12.3770-3775.2002.

Abstract

The 6-anilinouracils (AUs) constitute a new class of bactericidal antibiotics selective against gram-positive (Gr(+)) organisms. The AU family of compounds specifically inhibits a novel target, replicative DNA polymerase Pol IIIC. Like other antibiotics, AUs can be expected to engender the development of resistant bacteria. We have used a representative AU and clinically relevant strains of Staphylococcus aureus and Enterococcus to determine the frequency and mechanism(s) of resistance development. The frequency of resistance was determined by using N(3)-hydroxybutyl 6-(3'-ethyl-4'-methylanilino) uracil (HBEMAU) and commercially available antibiotics at eight times the MICs. For all five Gr(+) organisms tested, the frequency of resistance to HBEMAU ranged from 1 x 10(-8) to 3 x 10(-10). The frequencies of resistance to the antibiotics tested, including rifampin, gentamicin, and ciprofloxacin, were either greater than or equal to those for HBEMAU. In order to understand the mechanism of resistance, HBEMAU-resistant organisms were isolated. MIC assays showed that the organisms had increased resistance to AU inhibitors but not to other families of antibiotics. Inhibition studies with DNA polymerases from HBEMAU-sensitive and -resistant strains demonstrated that the resistance was associated with Pol IIIC. DNA sequence analysis of the entire polC genes from both wild-type and resistant organisms revealed that the resistant organisms had a sequence change that mapped to a single amino acid codon in all strains examined.

摘要

6-苯胺基尿嘧啶(AU)构成了一类对革兰氏阳性(Gr(+))菌具有选择性的新型杀菌抗生素。AU类化合物特异性抑制一种新型靶点——复制性DNA聚合酶Pol IIIC。与其他抗生素一样,预计AU会促使耐药菌的产生。我们使用了一种代表性的AU以及金黄色葡萄球菌和肠球菌的临床相关菌株来确定耐药性产生的频率和机制。通过使用N(3)-羟丁基6-(3'-乙基-4'-甲基苯胺基)尿嘧啶(HBEMAU)和八倍于最低抑菌浓度(MIC)的市售抗生素来确定耐药频率。对于所测试的所有五种Gr(+)菌,对HBEMAU的耐药频率范围为1×10(-8)至3×10(-10)。对所测试抗生素(包括利福平、庆大霉素和环丙沙星)的耐药频率要么大于要么等于对HBEMAU的耐药频率。为了了解耐药机制,分离出了对HBEMAU耐药的菌株。MIC测定表明,这些菌株对AU抑制剂的耐药性增加,但对其他抗生素家族没有耐药性。对来自对HBEMAU敏感和耐药菌株的DNA聚合酶的抑制研究表明,耐药性与Pol IIIC有关。对野生型和耐药菌株的整个polC基因进行DNA序列分析表明,耐药菌株的序列变化映射到所有检测菌株中的一个单一氨基酸密码子。

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