Alyamani Essam J, Khiyami Anamil M, Booq Rayan Y, Majrashi Majed A, Bahwerth Fayez S, Rechkina Elena
National Center for Biotechnology, King Abdulaziz City for Science and Technology, P.O. Box 6086, Riyadh, 11442, Saudi Arabia.
College of Medicine, Princess Nora Bint Abdul Rahman University, Riyadh, 12484, Saudi Arabia.
Ann Clin Microbiol Antimicrob. 2017 Jan 6;16(1):1. doi: 10.1186/s12941-016-0177-6.
The infection and prevalence of extended-spectrum β-lactamases (ESBLs) is a worldwide problem, and the presence of ESBLs varies between countries. In this study, we investigated the occurrence of plasmid-mediated ESBL/AmpC/carbapenemase/aminoglycoside resistance gene expression in Escherichia coli using phenotypic and genotypic techniques.
A total of 58 E. coli isolates were collected from hospitals in the city of Makkah and screened for the production of ESBL/AmpC/carbapenemase/aminoglycoside resistance genes. All samples were subjected to phenotypic and genotypic analyses. The antibiotic susceptibility of the E. coli isolates was determined using the Vitek-2 system and the minimum inhibitory concentration (MIC) assay. Antimicrobial agents tested using the Vitek 2 system and MIC assay included the expanded-spectrum (or third-generation) cephalosporins (e.g., cefoxitin, cefepime, aztreonam, cefotaxime, ceftriaxone, and ceftazidime) and carbapenems (meropenem and imipenem). Reported positive isolates were investigated using genotyping technology (oligonucleotide microarray-based assay and PCR). The genotyping investigation was focused on ESBL variants and the AmpC, carbapenemase and aminoglycoside resistance genes. E. coli was phylogenetically grouped, and the clonality of the isolates was studied using multilocus sequence typing (MLST).
Our E. coli isolates exhibited different levels of resistance to ESBL drugs, including ampicillin (96.61%), cefoxitin (15.25%), ciprofloxacin (79.66%), cefepime (75.58%), aztreonam (89.83%), cefotaxime (76.27%), ceftazidime (81.36%), meropenem (0%) and imipenem (0%). Furthermore, the distribution of ESBL-producing E. coli was consistent with the data obtained using an oligonucleotide microarray-based assay and PCR genotyping against genes associated with β-lactam resistance. ST131 was the dominant sequence type lineage of the isolates and was the most uropathogenic E. coli lineage. The E. coli isolates also carried aminoglycoside resistance genes.
The evolution and prevalence of ESBL-producing E. coli may be rapidly accelerating in Saudi Arabia due to the high visitation seasons (especially to the city of Makkah). The health authority in Saudi Arabia should monitor the level of drug resistance in all general hospitals to reduce the increasing trend of microbial drug resistance and the impact on patient therapy.
超广谱β-内酰胺酶(ESBLs)的感染与流行是一个全球性问题,且不同国家ESBLs的存在情况有所差异。在本研究中,我们运用表型和基因型技术调查了大肠杆菌中质粒介导的ESBL/AmpC/碳青霉烯酶/氨基糖苷类耐药基因的表达情况。
从麦加市的医院共收集了58株大肠杆菌分离株,并对其进行ESBL/AmpC/碳青霉烯酶/氨基糖苷类耐药基因产生情况的筛查。所有样本均进行表型和基因型分析。使用Vitek-2系统和最低抑菌浓度(MIC)测定法确定大肠杆菌分离株的抗生素敏感性。使用Vitek 2系统和MIC测定法检测的抗菌药物包括广谱(或第三代)头孢菌素(如头孢西丁、头孢吡肟、氨曲南、头孢噻肟、头孢曲松和头孢他啶)和碳青霉烯类(美罗培南和亚胺培南)。对报告的阳性分离株使用基因分型技术(基于寡核苷酸微阵列的检测和PCR)进行调查。基因分型调查聚焦于ESBL变体以及AmpC、碳青霉烯酶和氨基糖苷类耐药基因。对大肠杆菌进行系统发育分组,并使用多位点序列分型(MLST)研究分离株的克隆性。
我们的大肠杆菌分离株对ESBL药物表现出不同程度的耐药性,包括氨苄西林(96.61%)、头孢西丁(15.25%)、环丙沙星(79.66%)、头孢吡肟(75.58%)、氨曲南(89.83%)、头孢噻肟(76.27%)、头孢他啶(81.36%)、美罗培南(0%)和亚胺培南(0%)。此外,产ESBL大肠杆菌的分布与使用基于寡核苷酸微阵列的检测和针对与β-内酰胺耐药相关基因的PCR基因分型所获得的数据一致。ST131是分离株的主要序列类型谱系,也是最常见的尿路致病性大肠杆菌谱系。大肠杆菌分离株还携带氨基糖苷类耐药基因。
由于高访问季节(尤其是到麦加市),沙特阿拉伯产ESBL大肠杆菌的演变和流行可能正在迅速加速。沙特阿拉伯的卫生当局应监测所有综合医院的耐药水平,以降低微生物耐药性的上升趋势及其对患者治疗的影响。