Görgeç Sündüz, Kuzucu Çiğdem, Otlu Barış, Yetkin Funda, Ersoy Yasemin
Malatya Public Health Laboratory, Malatya, Turkey.
Mikrobiyol Bul. 2015 Jan;49(1):15-25. doi: 10.5578/mb.8437.
Extended-spectrum beta-lactamase (ESBL) producing microorganisms currently cause a major problem. Among theseCTX-M beta-lactamase producing Escherichia coli has also disseminated worldwide as an important cause of both nosocomial and community-acquired infections. The aims of this study were to determine the prevalence of the beta-lactamase genes, antibiotic susceptibilities and clonal relationships of ESBL-producing nosocomial E.coli isolates. A total of 76 ESBL-producing E.coli strains isolated from urine (n= 26), blood (n= 25) and wound (n= 25) specimens of hospitalized patients identified as nosocomial infection agents according to the CDC criteria between June 2010-June 2011 were included in the study. Antibiotic susceptibilities of the isolates were detected by Kirby-Bauer disc diffusion method according to CLSI recommendations. ESBL production was tested by double disc diffusion method, and cefotaxime/cefotaxime-clavulanic acid E-test strips (AB Biodisk, Sweden) were used for indeterminate results. Presence of TEM, SHV, CTX-M, OXA-2 group, 0XA-10 group, PER, VEB and GES beta-lactamase genes were investigated by polymerase chain reaction (PCR) using specific primers. Pulsed-field gel electrophoresis (PFGE) method was used for the detection of clonal relationships among the strains. Most of the ESBL-producing E.coli strains were isolated from samples of inpatients in intensive care (35%), internal medicine (16%) and general surgery (13%) units. All of the 76 strains were found susceptible to imipenem, meropenem and amikacin; however all were resistant to cefotaxime and ceftriaxone. The susceptibility rates of the isolates to cefoxitin, ertapenem, cefoperazone/sulbactam, piperacillin-tazobactam, gentamicin, ciprofloxacin, cefepime, amoxicillin-clavulanic acid, aztreonam and ceftazidime were 96%, 83%, 63%, 61%, 50%, 41%, 25%, 21%, 20% and 18%, respectively. Among E.coli isolates, the frequency of CTX-M, TEM, OXA-2 group, PER, SHV and OXA-10 group beta-lactamase genes were found as 89.5%, 59.2%, 15.8%, 14.5%, 11.8% and 3.9%, respectively, while none of the isolates were positive for VEB and GES beta-lactamase genes. In 1 (1.3%) strain none of the investigated genes were detected. PCR analyses of the isolates revealed that 25 harbored CTX-M and TEM genes together, while 20 harbored only CTX-M and two harbored only TEM genes. Single SHV gene was not detected in any of the isolates. PFGE demonstrated no major clonal relationship between ESBL-producing isolates. This study indicated that CTX-M type enzymes were highly endemic among ESBL-producing nosocomial E.coli strains in our hospital, with the polyclonal spread of ESBL-producing bacteria without any dominant epidemic clone. In conclusion, it was considered that further studies are needed to explain the relationship between epidemic clones and plasmids with the use of plasmid analysis and multilocus sequence typing methods.
产超广谱β-内酰胺酶(ESBL)的微生物目前引发了一个重大问题。其中,产CTX-Mβ-内酰胺酶的大肠埃希菌也已在全球范围内传播,成为医院感染和社区获得性感染的重要病因。本研究的目的是确定产ESBL的医院内大肠埃希菌分离株中β-内酰胺酶基因的流行情况、抗生素敏感性及克隆关系。本研究纳入了2010年6月至2011年6月期间,根据美国疾病控制与预防中心(CDC)标准,从住院患者的尿液(n = 26)、血液(n = 25)和伤口(n = 25)标本中分离出的76株产ESBL的大肠埃希菌菌株,这些菌株被确定为医院感染病原体。根据美国临床和实验室标准协会(CLSI)的建议,采用 Kirby-Bauer 纸片扩散法检测分离株的抗生素敏感性。通过双纸片扩散法检测ESBL的产生情况,对于不确定结果,使用头孢噻肟/头孢噻肟-克拉维酸E-test试纸条(瑞典AB Biodisk公司)。使用特异性引物通过聚合酶链反应(PCR)研究TEM、SHV、CTX-M、OXA-2组、OXA-10组、PER、VEB和GESβ-内酰胺酶基因的存在情况。采用脉冲场凝胶电泳(PFGE)方法检测菌株之间的克隆关系。大多数产ESBL的大肠埃希菌菌株分离自重症监护病房(35%)、内科(16%)和普通外科(13%)病房住院患者的样本。76株菌株均对亚胺培南、美罗培南和阿米卡星敏感;然而,所有菌株均对头孢噻肟和头孢曲松耐药。分离株对头孢西丁、厄他培南、头孢哌酮/舒巴坦、哌拉西林-他唑巴坦、庆大霉素、环丙沙星、头孢吡肟、阿莫西林-克拉维酸、氨曲南和头孢他啶的敏感率分别为96%、83%、63%、61%