Suppr超能文献

20 多年来德国分离的人型支原体和脲原体对四环素类、大环内酯类、氟喹诺酮类和克林霉素的体外活性。

In-vitro activities of tetracyclines, macrolides, fluoroquinolones and clindamycin against Mycoplasma hominis and Ureaplasma ssp. isolated in Germany over 20 years.

机构信息

Institute for Infection Medicine, University Medical Center Schleswig-Holstein, Christian Albrecht University of Kiel, Germany.

出版信息

Clin Microbiol Infect. 2010 Nov;16(11):1649-55. doi: 10.1111/j.1469-0691.2009.03155.x.

Abstract

Antimicrobial resistance in genital mycoplasmas is increasing and shows global variation. We determined the susceptibilities of 469 mycoplamas, comprising 290 Mycoplasma hominis and 179 ureaplasma isolates collected during 1983 and 1989-2004, to eleven antibacterials by agar dilution. Additionally, we analyzed the results of routine E-testing during 2005-2008. Doxycycline was the most active tetracycline with (MIC₉₀ of 1 and 8 mg/L for ureaplasmas and M. hominis, respectively. Significantly more M. hominis isolates (approximately 10-13%) than ureaplasmas (approximately 1-3%) were resistant to tetracyclines. Ofloxacin was effective against both species (>95% susceptibility). Ciprofloxacin was moderately active against M. hominis and less active against ureaplasmas (70.3% and 35.2% susceptibility, respectively). Clarithromycin and josamycin were the most potent macrolides (MIC₉₀ of 0.5 mg/L) against ureaplasmas. Erythromycin had the lowest activity (MIC₉₀ of 8 mg/L) against ureaplasmas like clindamycin which was the most potent agent against M. hominis. Cross-resistance was found between tetracyclines (53-93%), macrolides and erythromycin (70-100%), and between erythromycin and ciprofloxacin (43-55%). M. hominis became more resistant to tetracyclines and fluoroquinolones between 1989 and 2004, although there was little change during 2005-2008. Ureaplasmas became more resistant to cipfloxacin during 1997 – 2004 and showed high resistance rates to erythromycin during 1989-2008. Doxycycline is still the drug of first-choice for the treatment of ureaplasmal infections and may be used for co-infection with M. hominis.

摘要

生殖器支原体的抗菌药物耐药性正在增加,并表现出全球性的差异。我们通过琼脂稀释法测定了 1983 年至 1989 年至 2004 年间收集的 290 株人型支原体和 179 株解脲支原体中 469 株支原体对 11 种抗菌药物的敏感性。此外,我们还分析了 2005 年至 2008 年常规 E 试验的结果。强力霉素是最有效的四环素,解脲支原体和人型支原体的 MIC₉₀分别为 1 和 8mg/L。与解脲支原体(约 1-3%)相比,人型支原体(约 10-13%)对四环素的耐药性显著增加。氧氟沙星对两种支原体均有效(>95%的敏感性)。环丙沙星对人型支原体具有中等活性,对解脲支原体的活性较低(分别为 70.3%和 35.2%的敏感性)。克拉霉素和交沙霉素是治疗解脲支原体最有效的大环内酯类药物(MIC₉₀为 0.5mg/L)。红霉素对解脲支原体的活性最低(MIC₉₀为 8mg/L),与克林霉素相似,克林霉素是人型支原体最有效的药物。四环素(53-93%)、大环内酯类和红霉素(70-100%)以及红霉素和环丙沙星(43-55%)之间存在交叉耐药性。1989 年至 2004 年间,人型支原体对四环素和氟喹诺酮类药物的耐药性增加,尽管 2005 年至 2008 年间变化不大。1997 年至 2004 年间,解脲支原体对环丙沙星的耐药性增加,1989 年至 2008 年间对红霉素的耐药率较高。强力霉素仍然是治疗解脲支原体感染的首选药物,也可用于与人型支原体的混合感染。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验