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首页> 外文期刊>Frontiers in Microbiology >Update on infections caused by Stenotrophomonas maltophilia with particular attention to resistance mechanisms and therapeutic options
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Update on infections caused by Stenotrophomonas maltophilia with particular attention to resistance mechanisms and therapeutic options

机译:嗜麦芽窄食单胞菌引起的感染的最新进展,尤其要注意耐药机制和治疗选择

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Stenotrophomonas maltophilia is a Gram-negative, biofilm-forming bacterium. Although generally regarded as an organism of low virulence, S. maltophilia is an emerging multi-drug resistant opportunistic pathogen in hospital and community settings, especially among immunocompromised hosts. Risk factors associated with S. maltophilia infection include underlying malignancy, cystic fibrosis, corticosteroid or immunosuppressant therapy, the presence of an indwelling central venous catheter and exposure to broad spectrum antibiotics. In this review, we provide a synthesis of information on current global trends in S. maltophilia pathogenicity as well as updated information on the molecular mechanisms contributing to its resistance to an array of antimicrobial agents. The prevalence of S. maltophilia infection in the general population increased from 0.8–1.4% during 1997–2003 to 1.3–1.68% during 2007–2012. The most important molecular mechanisms contributing to its resistance to antibiotics include β-lactamase production, the expression of Qnr genes, and the presence of class 1 integrons and efflux pumps. Trimethoprim/sulfamethoxazole (TMP/SMX) is the antimicrobial drug of choice. Although a few studies have reported increased resistance to TMP/SMX, the majority of studies worldwide show that S. maltophilia continues to be highly susceptible. Drugs with historically good susceptibility results include ceftazidime, ticarcillin-clavulanate, and fluoroquinolones; however, a number of studies show an alarming trend in resistance to those agents. Tetracyclines such as tigecycline, minocycline, and doxycycline are also effective agents and consistently display good activity against S. maltophilia in various geographic regions and across different time periods. Combination therapies, novel agents, and aerosolized forms of antimicrobial drugs are currently being tested for their ability to treat infections caused by this multi-drug resistant organism.
机译:嗜麦芽窄食单胞菌是革兰氏阴性生物膜形成细菌。尽管通常被认为是低毒力生物,但在医院和社区环境中,特别是在免疫功能低下的宿主中,嗜麦芽孢杆菌是一种新兴的多药耐药性病原体。与嗜麦芽孢杆菌感染相关的危险因素包括潜在的恶性肿瘤,囊性纤维化,皮质类固醇或免疫抑制剂治疗,留置中心静脉导管的存在以及接触广谱抗生素。在这篇综述中,我们提供了有关嗜麦芽链球菌致病性当前全球趋势的信息综述,以及有关导致其对一系列抗菌剂耐药的分子机制的最新信息。普通人群嗜麦芽孢杆菌感染的患病率从1997-2003年的0.8-1.4%增加到2007-2012年的1.3-1.68%。导致其对抗生素产生抗性的最重要分子机制包括β-内酰胺酶的产生,Qnr基因的表达以及1类整合素和外排泵的存在。甲氧苄氨嘧啶/磺胺甲基异恶唑(TMP / SMX)是首选的抗菌药物。尽管少数研究报告了对TMP / SMX的耐药性增强,但全世界的大多数研究表明,嗜麦芽养链球菌仍然高度易感。历史上具有良好敏感性的药物包括头孢他啶,替卡西林-克拉维酸盐和氟喹诺酮类;但是,许多研究表明,对这些药物的抗药性趋势惊人。四环素,例如替加环素,米诺环素和强力霉素也是有效的药物,并且在不同的地理区域和不同的时间段内始终表现出良好的抗嗜麦芽链球菌的活性。目前正在测试组合疗法,新型药物和气雾化形式的抗菌药物治疗由这种多药耐药生物引起的感染的能力。

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