Ghotaslou Reza, Sadeghi Mohammad Reza, Akhi Mohammad Taghi, Hasani Alka, Asgharzadeh Mohammad
Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Department of Microbiology, School of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.
Iran J Pharm Res. 2018 Winter;17(Suppl):79-88.
The current study was conducted to determine prevalence and antimicrobial susceptibility patterns, ESBL, AmpC and carbapenemase- producers among clinical isolates of . Three hundred and seven non-duplicative clinical isolates were collected from hospitalized patients in five medical centers in Azerbaijan, Iran. Initial screening for β-lactamase production was performed using disc agar diffusion according to Clinical Laboratory Standards Institute (CLSI) guidelines. Phenotypic confirmatory tests was done using total ESBL/AmpC confirm kit, KPC/MBL and OXA-48 confirm kit according to manufacturer's instructions. The overall prevalence of ESBL, AmpC, and carbapenemase-producing strains were 42.7% (131/307), 14.0%(43/307) and 4.9% (15/307), respectively. The prevalence of ESBLs was 38.35%, 64.9% and 35.7% for , and respectively. Carbapenemase activity was only observed among 15 isolates and detected phenotypes include MBL (9/57, 15.8%), KPC (4/57, 7.0%), and OXA-48 (2/57, 3.5%). Fourteen out of 307 isolates (4.6%) were recognized to have ESBL or AmpC hyper-producer with decreased cell wall permeability phenotype. All 4 shigella strains were positive for ESBL and 4 isolates of , 2 isolates of and 1 seratia spp. were detected as AmpC producer. The only strain isolated was positive for both ESBL and AmpC. This study reveals high prevalence of multidrug-resistant (MDR) β-lactamase-producing reaching 89.5%. Imipenem and meropenem showed potent antibacterial activities against all MDR β-lactamase-producers except for carbapenemase producers. After carbapenems, amikacin, piperacillin/tazobactam and amoxicillin/clavulanic acid were second the most effective drugs against β-lactamase-producing isolates.
本研究旨在确定[具体研究对象]临床分离株中ESBL、AmpC和碳青霉烯酶产生菌的流行率及抗菌药物敏感性模式。从伊朗阿塞拜疆的五个医疗中心的住院患者中收集了307株非重复临床分离株。根据临床实验室标准协会(CLSI)指南,使用纸片琼脂扩散法对β-内酰胺酶产生情况进行初步筛查。根据制造商的说明,使用总ESBL/AmpC确认试剂盒、KPC/MBL和OXA-48确认试剂盒进行表型确证试验。产ESBL、AmpC和碳青霉烯酶菌株的总体流行率分别为42.7%(131/307)、14.0%(43/307)和4.9%(15/307)。[具体研究对象1]、[具体研究对象2]和[具体研究对象3]的ESBLs流行率分别为38.35%、64.9%和35.7%。仅在15株[具体研究对象]分离株中观察到碳青霉烯酶活性,检测到的表型包括MBL(9/57,15.8%)、KPC(4/57,7.0%)和OXA-48(2/57,3.5%)。307株分离株中有14株(4.6%)被鉴定为具有细胞壁通透性降低表型的ESBL或AmpC高产菌。所有4株志贺氏菌属菌株ESBL均为阳性,4株[具体研究对象1]、2株[具体研究对象2]和1株沙雷氏菌属菌株被检测为AmpC产生菌。分离出的唯一1株[具体研究对象]菌株ESBL和AmpC均为阳性。本研究显示产多药耐药(MDR)β-内酰胺酶的[具体研究对象]的流行率很高,达到89.5%。亚胺培南和美罗培南对除碳青霉烯酶产生菌外的所有MDRβ-内酰胺酶产生菌均显示出强大的抗菌活性。在碳青霉烯类药物之后,阿米卡星、哌拉西林/他唑巴坦和阿莫西林/克拉维酸是对产β-内酰胺酶的[具体研究对象]分离株第二有效的药物。