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Low frequencies of resistance among Staphylococcus and Enterococcus species to the bactericidal DNA polymerase inhibitor N(3)-hydroxybutyl 6-(3'-ethyl-4'-methylanilino) uracil.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。
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2
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In vitro antimicrobial activities of novel anilinouracils which selectively inhibit DNA polymerase III of gram-positive bacteria.新型苯胺基脲嘧啶的体外抗菌活性,其可选择性抑制革兰氏阳性菌的DNA聚合酶III。
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本文引用的文献

1
Mechanisms and frequency of resistance to premafloxacin in Staphylococcus aureus: novel mutations suggest novel drug-target interactions.金黄色葡萄球菌对普马沙星的耐药机制及频率:新突变提示新的药物-靶点相互作用
Antimicrob Agents Chemother. 2000 Dec;44(12):3344-50. doi: 10.1128/AAC.44.12.3344-3350.2000.
2
In vitro antimicrobial activities of novel anilinouracils which selectively inhibit DNA polymerase III of gram-positive bacteria.新型苯胺基脲嘧啶的体外抗菌活性,其可选择性抑制革兰氏阳性菌的DNA聚合酶III。
Antimicrob Agents Chemother. 2000 Aug;44(8):2217-21. doi: 10.1128/AAC.44.8.2217-2221.2000.
3
Inhibitors of DNA polymerase III as novel antimicrobial agents against gram-positive eubacteria.DNA聚合酶III抑制剂作为抗革兰氏阳性真细菌的新型抗菌剂。
Antimicrob Agents Chemother. 1999 Aug;43(8):1982-7. doi: 10.1128/AAC.43.8.1982.
4
Analysis of vancomycin population susceptibility profiles, killing activity, and postantibiotic effect against vancomycin-intermediate Staphylococcus aureus.针对万古霉素中介金黄色葡萄球菌的万古霉素群体药敏谱、杀菌活性及抗生素后效应分析。
Antimicrob Agents Chemother. 1999 Aug;43(8):1914-8. doi: 10.1128/AAC.43.8.1914.
5
6-Anilinouracil-based inhibitors of Bacillus subtilis DNA polymerase III: antipolymerase and antimicrobial structure-activity relationships based on substitution at uracil N3.基于6-苯胺基尿嘧啶的枯草芽孢杆菌DNA聚合酶III抑制剂:基于尿嘧啶N3取代的抗聚合酶和抗菌构效关系
J Med Chem. 1999 Jun 3;42(11):2035-40. doi: 10.1021/jm980693i.
6
The hyperthermophilic bacterium Thermotoga maritima has two different classes of family C DNA polymerases: evolutionary implications.嗜热栖热菌(Thermotoga maritima)这种嗜热细菌拥有两类不同的C家族DNA聚合酶:进化意义。
Nucleic Acids Res. 1998 Dec 1;26(23):5300-9. doi: 10.1093/nar/26.23.5300.
7
DNA polymerase III of Gram-positive eubacteria is a zinc metalloprotein conserving an essential finger-like domain.革兰氏阳性真细菌的DNA聚合酶III是一种保留了必需指状结构域的锌金属蛋白。
Biochemistry. 1998 Nov 3;37(44):15254-60. doi: 10.1021/bi981113m.
8
Bacterial resistance: a worldwide problem.细菌耐药性:一个全球性问题。
Diagn Microbiol Infect Dis. 1998 Jun;31(2):379-88. doi: 10.1016/s0732-8893(98)00037-6.
9
Multiple-drug resistant enterococci: the nature of the problem and an agenda for the future.多重耐药肠球菌:问题的本质与未来议程
Emerg Infect Dis. 1998 Apr-Jun;4(2):239-49. doi: 10.3201/eid0402.980211.
10
Selection of fluoroquinolone-resistant methicillin-resistant Staphylococcus aureus with ciprofloxacin and trovafloxacin.用环丙沙星和曲伐沙星筛选耐氟喹诺酮的耐甲氧西林金黄色葡萄球菌。
Antimicrob Agents Chemother. 1998 Mar;42(3):727. doi: 10.1128/AAC.42.3.727.

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.

DOI:10.1128/AAC.46.12.3770-3775.2002
PMID:12435675
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC132772/
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。