Suppr超能文献

长期口服大环内酯类药物治疗痤疮会增加耐大环内酯类痤疮丙酸杆菌。

Long-term administration of oral macrolides for acne treatment increases macrolide-resistant Propionibacterium acnes.

机构信息

Department of Microbiology, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, Tokyo, Japan.

出版信息

J Dermatol. 2018 Mar;45(3):340-343. doi: 10.1111/1346-8138.14178. Epub 2017 Dec 13.

Abstract

Macrolide-resistant Propionibacterium acnes are frequently isolated from patients with acne vulgaris, and the most resistant isolates (>90% resistance) have the 23S rRNA mutation. An increase in resistant P. acnes with this mutation is thought to be caused by the inappropriate use of antimicrobials. Therefore, we studied the mutation frequency of macrolide resistance in P. acnes in vitro. When P. acnes mutants were exposed to clarithromycin after being incubated in broth without antimicrobials, resistant mutants with the 23S rRNA mutation were not isolated. However, the mutants were obtained at the frequency of 10 after being pre-incubated with 0.03 μg/mL of antimicrobials. This is the estimated epidermal concentration of clarithromycin after p.o. administration. The resistant mutants had the 23S rRNA mutations A2058G, A2059G and C2611G. When pre-incubated with clarithromycin, C2611G mutants which showed resistance to clarithromycin were obtained 32.1% more often than pre-incubated with clindamycin (P < 0.01). By contrast, when pre-incubated with clindamycin, A2058G mutants, which show high-level resistance to both clarithromycin and clindamycin, were more frequently obtained than pre-incubated with clarithromycin (87.5%, P < 0.01). No difference in the isolation rate of A2059G mutants, which show high-level resistance to macrolides but low-level resistance to clindamycin, was found with either treatment. These results indicate the possibility that long-term use of oral macrolides for acne treatment facilitate the increase of macrolide-resistant P. acnes.

摘要

痤疮丙酸杆菌对大环内酯类药物的耐药性经常从寻常痤疮患者中分离出来,最耐药的分离株(>90%的耐药性)具有 23S rRNA 突变。携带这种突变的耐药性痤疮丙酸杆菌的增加被认为是由于抗菌药物的不当使用。因此,我们研究了体外痤疮丙酸杆菌对大环内酯类药物耐药性的突变频率。当在没有抗菌药物的肉汤中孵育后,将痤疮丙酸杆菌突变体暴露于克拉霉素中时,未分离到具有 23S rRNA 突变的耐药突变体。然而,当预先用 0.03μg/mL 的抗菌药物孵育时,以 10 的频率获得了突变体。这是口服给药后克拉霉素在表皮中的估计浓度。耐药突变体具有 23S rRNA 突变 A2058G、A2059G 和 C2611G。当用克拉霉素预先孵育时,获得对克拉霉素耐药的 C2611G 突变体的频率比用克林霉素(P < 0.01)预先孵育时高 32.1%。相比之下,当用克林霉素预先孵育时,与克拉霉素相比,高水平耐药克拉霉素和克林霉素的 A2058G 突变体更容易获得(87.5%,P < 0.01)。无论用哪种药物处理,高水平耐药克拉霉素和克林霉素、低水平耐药克林霉素的 A2059G 突变体的分离率均无差异。这些结果表明,长期使用口服大环内酯类药物治疗痤疮可能会增加耐大环内酯类的痤疮丙酸杆菌。

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