Aris Parisa, Boroumand Mohammad Ali, Rahbar Mohammad, Douraghi Masoumeh
1 Division of Microbiology, Department of Pathobiology, School of Public Health, Tehran University of Medical Sciences , Tehran, Iran .
2 Department of Pathology, Tehran Heart Center, Tehran University of Medical Sciences , Tehran, Iran .
Microb Drug Resist. 2018 Jun;24(5):607-612. doi: 10.1089/mdr.2017.0097. Epub 2017 Oct 24.
Despite global efforts to tackle resistance in extended-spectrum beta-lactamase (ESBL)-producing isolates via old antibiotics, there are limited data on the efficacy of fosfomycin-an old oral antibiotic-against Enterobacteriaceae in the Middle East. The purpose of this study was to evaluate the in vitro activity of fosfomycin against urinary ESBL-producing isolates of Enterobacteriaceae. Between 2004 and 2015, 363 isolates of ESBL-producing Enterobacteriaceae were recovered from high-risk patients suffering from cardiac disorders and were subjected to polymerase chain reaction using specific primers for the bla, bla, and bla genes. Antibiotic susceptibility testing was performed for fosfomycin and other antibiotic comparators. For the isolates considered nonsusceptible to fosfomycin by disk diffusion, the minimum inhibitory concentration (MIC) was determined. The susceptibility rate to fosfomycin remained almost steady (90-100%) over a 12-year period, although it fluctuated vis-à-vis ciprofloxacin (0-54%), trimethoprim/sulfamethoxazole (9.1-31.7%), and nitrofurantoin (41.7-100%). Of all the antibiotics tested, fosfomycin was the most active antimicrobial agent (97%) against the ESBL-positive isolates. Fosfomycin maintained higher activity against ESBL-Escherichia coli than against ESBL-Klebsiella pneumoniae. Only 11 (3%) isolates were not susceptible to fosfomycin according to disk diffusion and they had MICs greater than 1,024 mg/ml. All of the fosfomycin-nonsusceptible isolates were positive for the bla gene (100%), while 5 (45.4%) and 3 (27.3%) of the isolates harbored the bla and bla genes, respectively. We showed that fosfomycin had a numerically higher susceptibility rate than the other antibiotics against the ESBL-producing isolates of the most common Enterobacteriaceae. Given its low resistance rate and oral administration, fosfomycin may be deemed a promising antibiotic for the treatment of urinary tract infections caused by ESBL-producing Enterobacteriaceae.
尽管全球都在努力通过老抗生素应对产超广谱β-内酰胺酶(ESBL)菌株的耐药性问题,但关于磷霉素(一种老的口服抗生素)对中东地区肠杆菌科细菌疗效的数据有限。本研究的目的是评估磷霉素对产ESBL的尿路肠杆菌科分离株的体外活性。2004年至2015年期间,从患有心脏疾病的高危患者中分离出363株产ESBL的肠杆菌科细菌,并使用针对bla、bla和bla基因的特异性引物进行聚合酶链反应。对磷霉素和其他抗生素对照品进行了药敏试验。对于纸片扩散法判定对磷霉素不敏感的分离株,测定其最低抑菌浓度(MIC)。在12年期间,磷霉素的敏感率几乎保持稳定(90 - 100%),尽管相对于环丙沙星(0 - 54%)、甲氧苄啶/磺胺甲恶唑(9.1 - 31.7%)和呋喃妥因(41.7 - 100%)有所波动。在所有测试的抗生素中,磷霉素是对ESBL阳性分离株活性最高的抗菌剂(97%)。磷霉素对产ESBL的大肠埃希菌的活性高于产ESBL的肺炎克雷伯菌。根据纸片扩散法,只有11株(3%)分离株对磷霉素不敏感,其MIC大于1024mg/ml。所有对磷霉素不敏感的分离株bla基因均为阳性(100%),而分别有5株(45.4%)和3株(27.3%)分离株携带bla和bla基因。我们表明,在针对最常见的产ESBL肠杆菌科分离株方面,磷霉素的敏感率在数值上高于其他抗生素。鉴于其低耐药率和口服给药方式,磷霉素可能被认为是治疗产ESBL肠杆菌科细菌引起的尿路感染的一种有前景的抗生素。