期刊文献+

肺炎支原体对大环内酯类抗生素耐药机制的研究进展 被引量:8

Research progress in mechanisms of drug-resistance of macrolide antibiotics resistance in Mycoplasma pneumoniae
下载PDF
导出
摘要 大环内酯类抗生素是治疗儿童肺炎支原体(MP)感染的一线药物,但随着此类药物在临床中的广泛使用,对大环内酯类抗生素耐药的MP菌株检出率迅速增高。耐药机制相关研究中,对药物作用靶点的研究最多见,其中23S rRNA基因突变相关研究尤为广泛和深入。耐药性会影响药物治疗效果,探讨菌株对药物的耐药机制并合理调整药物治疗方案,可获得更好的治疗效果,现将大环内酯类抗生素的作用机制和MP对大环内酯类抗生素的耐药机制综述如下。 Macrolide antibiotics are the first-line drugs for the treatment of Mycoplasma pneumoniae(MP)infections in children,but with the increased use of macrolides,the detection rate of resistant strains of MP to macrolides has increased rapidly.Among the studies related to the mechanisms of drug resistance,the study of drug targets has been the most extensive and intensive,with mutations in the 23S rRNA gene being studied most extensively.The emergence of drug resistance affects the therapeutic efficacy of drugs,and the mechanisms of drug resistance need to be explored to adjust the choice of therapeutic agents in order to achieve higher therapeutic efficacy.This paper reviewed the mechanisms of action of macrolides and the mechanisms of resistance to macrolides by MP.
作者 汪慧华 邹映雪 WANG Huihua;ZOU Yingxue(Postgraduate College of Tianjin Medical University,Tianjin,300350;Respiratory Department,Tianjin Children′s Hospital,Tianjin,300350)
出处 《实用临床医药杂志》 2023年第12期136-140,148,共6页 Journal of Clinical Medicine in Practice
基金 天津市卫健委重点学科专项课题(TJWJ2022XK038) 天津市医学重点学科(专科)建设项目资助(TJYXZDXK-040A)。
关键词 肺炎支原体 大环内酯类抗生素 耐药机制 儿童 基因突变 Mycoplasma pneumoniae macrolide antibiotics drug resistance mechanisms children gene mutations
  • 相关文献

参考文献7

二级参考文献56

  • 1宋琳,瞿介明,何礼贤,张丽珺,丁廷波.肺炎链球菌对大环内酯类抗生素耐药情况及耐药基因研究[J].中国感染与化疗杂志,2006,6(2):127-129. 被引量:8
  • 2慢性阻塞性肺疾病诊治指南(2007年修订版)[J].中华内科杂志,2007,46(3):254-261. 被引量:1794
  • 3SzczypaK,Sadowy E,Izdebski R,et al.Group A Streptococci from in-vasive -disease episodes in Poland are remarkably divergent at themolecular level[J].J Clin Microbiol ,2006,40(11) : 3975-3979.
  • 4FarrellDJ.Douthwaite S, Morrissey I,ef al.Macrolide resistance by ri-bosomal mutation in clinical isolates of Strepto -coccus pneumoniaefrom the PROTEKT 1999-2000 study[J].Antimicrob Agents Chemoth-er,2003,47(6):1777-1783.
  • 5Waites KB, Talkington DF. Mycoplasma pneumoniae and its role as a human pathogen [ J]. Clin Microbiol Rev, 2004, 17 (4) : 697-728. DOI : 10.1128/CMR. 17.4. 697-728. 2004.
  • 6Atkinson TP, Balish MF, Waites KB. Epidemiology, clinical manifestations, pathogenesis and laboratory detection of Mycoplasma pneumoniae infections [ J ]. FEMS Microbiol Rev, 2008, 32 (6) : 956-973. DOI: 10. llll/j. 1574-6976. 2008. 00129. x.
  • 7Waites KB, Balish MF, Atkinson TP. New insights into the pathogenesis and detection of Mycoplasma pneumoniae infections [Jl. Future Mierobiol, 2008, 3 (6) :635-648. DOI: 10. 2217/ 17460913.3.6.635.
  • 8Himmelreieh R, Hilbert H, Plagens H, et al. Complete sequence analysis of the genome of the bacterium Mycoplasma pneumoniae [ J I. Nucleic Acids Res, 1996, 24 (22) : 4420 AA.49. DOI : 10. 1093/nar/24.22. 4420.
  • 9Miyata M. Gliding motility of mycoplasma-a mechanism cannot be explained by today's biology [ J ]. Nippon Saikingaku Zasshi,2002, 57(4) :581-595.
  • 10Baseman JB, Banai M, Kahane I. Sialic acid residues mediate Mycoplasma pneumoniae attachment to human and sheep erythrocytes [ J]. Infect Immun, 1982, 38(1 ) :389-391.

共引文献129

同被引文献83

引证文献8

二级引证文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部