Chang Ya-Ting, Lin Chun-Yu, Chen Yen-Hsu, Hsueh Po-Ren
Division of Infectious Diseases, Department of Internal Medicine, Kaohsiung Municipal HsiaoKang Hospital Kaohsiung, Taiwan ; Division of Infectious Diseases, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung Medical University Kaohsiung, Taiwan.
Division of Infectious Diseases, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung Medical University Kaohsiung, Taiwan ; School of Medicine, Graduate Institute of Medicine, Sepsis Research Center, College of Medicine, Kaohsiung Medical University Kaohsiung, Taiwan.
Front Microbiol. 2015 Sep 2;6:893. doi: 10.3389/fmicb.2015.00893. eCollection 2015.
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.
嗜麦芽窄食单胞菌是一种革兰氏阴性、形成生物膜的细菌。尽管通常被认为是一种毒力较低的微生物,但嗜麦芽窄食单胞菌在医院和社区环境中,尤其是在免疫功能低下的宿主中,正成为一种新兴的多重耐药机会致病菌。与嗜麦芽窄食单胞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、存在中心静脉留置导管以及接触广谱抗生素。在本综述中,我们综合了关于嗜麦芽窄食单胞菌致病性当前全球趋势的信息,以及关于其对一系列抗菌药物耐药性的分子机制的最新信息。嗜麦芽窄食单胞菌感染在普通人群中的患病率从1997 - 2003年的0.8 - 1.4%上升至2007 - 2012年的1.3 - 1.68%。导致其对抗生素耐药的最重要分子机制包括β - 内酰胺酶的产生、Qnr基因的表达、1类整合子的存在以及外排泵。甲氧苄啶/磺胺甲恶唑(TMP/SMX)是首选抗菌药物。尽管有一些研究报告对TMP/SMX的耐药性有所增加,但全球大多数研究表明嗜麦芽窄食单胞菌仍然高度敏感。历史上药敏结果良好的药物包括头孢他啶、替卡西林 - 克拉维酸和氟喹诺酮类;然而,多项研究显示对这些药物的耐药性呈惊人趋势。四环素类如替加环素、米诺环素和多西环素也是有效的药物,并且在不同地理区域和不同时间段对嗜麦芽窄食单胞菌始终表现出良好的活性。联合疗法、新型药物以及抗菌药物的雾化剂型目前正在测试其治疗由这种多重耐药菌引起的感染的能力。