Unlu Ozge, Demirci Mehmet
Beykent University School of Medicine, Department of Medical Microbiology, Istanbul, Turkey.
GMS Hyg Infect Control. 2020 Nov 30;15:Doc31. doi: 10.3205/dgkh000366. eCollection 2020.
Carbapenem-resistant (CR-Kp) strains are important nosocomial pathogens worldwide. In this study, we aimed to reveal the antibiotic resistance of clinical CR-Kp strains and determine the presence of KPC, OXA-48, VIM and IMP carbapenemase genes. CTX-M-1, TEM-1, SHV-1 extended-spectrum beta-lactamase (ESBL) genes, , , plasmid-mediated quinolone resistance genes and sul1 and sul2 sulfonamide resistance genes provided molecular epidemiological data. A total of 175 strains were isolated from clinical samples of patients hospitalised in an intensive care unit (ICU) betweent April and October 2017. The strains were identified with conventional methods, with VITEK 2 (BioMerieux, France) and MALDI-TOF MS (Bruker, USA). Antimicrobial susceptibilities were tested using the disc-diffusion method and E-test (BioMerieux, France). Antimicrobial resistance genes were investigated via real-time PCR in strains identified as CR-Kp. High frequencies of (86.36%), (86.36%), and (95.45%) genes were found in CR-Kp strains. Morever, all three ESBL genes coexisted in 77.3% of all strains. was detected in 12 (54.55%) of the strains, and 4 of them which had an MIC> 16 μg/mL to imipenem showed positivity as well. The gene determinant (86.36%) had the highest frequency, and strains carrying showed higher MICs for ciprofloxacin. CR-Kp strains are able to develop different antimicrobial resistance patterns according to regional changes in antimicrobial therapeutic policies. Thus, it is important to monitor the regional molecular epidemiological data for efficient treatment.
耐碳青霉烯类(CR-Kp)菌株是全球重要的医院病原体。在本研究中,我们旨在揭示临床CR-Kp菌株的抗生素耐药性,并确定KPC、OXA-48、VIM和IMP碳青霉烯酶基因的存在情况。CTX-M-1、TEM-1、SHV-1超广谱β-内酰胺酶(ESBL)基因、质粒介导的喹诺酮耐药基因以及sul1和sul2磺胺耐药基因提供了分子流行病学数据。2017年4月至10月期间,从重症监护病房(ICU)住院患者的临床样本中总共分离出175株菌株。采用传统方法、VITEK 2(法国生物梅里埃公司)和基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS,美国布鲁克公司)对菌株进行鉴定。使用纸片扩散法和E-test(法国生物梅里埃公司)检测抗菌药物敏感性。通过实时PCR对鉴定为CR-Kp的菌株中的抗菌药物耐药基因进行研究。在CR-Kp菌株中发现了高频率的(86.36%)、(86.36%)和(95.45%)基因。此外,所有三种ESBL基因在77.3%的菌株中共存。在12株(54.55%)菌株中检测到,其中4株对亚胺培南的最低抑菌浓度(MIC)>16μg/mL的菌株也显示为阳性。基因决定簇(86.36%)频率最高,携带该基因的菌株对环丙沙星显示出更高的MIC值。CR-Kp菌株能够根据抗菌治疗策略的区域变化形成不同的抗菌耐药模式。因此,监测区域分子流行病学数据对于有效治疗至关重要。