The Abundance of Plasmid-Mediated Quinolone Resistance Genes in Enterobacter cloacae Strains Isolated from Clinical Specimens in Kermanshah, Iran

Mandana Afsharian, Somayeh Asadi, Camellia Danesh, Reza Sedighi, Kohsar Karimi, Nooshin Miladi, Ronak Miladi, Mohsen Azizi, Nahid Madadi-Goli, Kamal Ahmadi, Mohammad Hossein Zamanian
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Abstract

Background. Enterobacter cloacae (E. cloacae) is one of the most common Enterobacteriaceae causing nosocomial infections. Plasmid-mediated quinolone resistance (PMQR) determinants have been considered recently. This study evaluated the abundance of PMQR genes in strains of E. cloacae obtained from clinical samples in Kermanshah, Iran. Methods. In this descriptive cross-sectional study, after collecting 113 isolates of E. cloacae, their identity was confirmed using specific biochemical tests. After determining their drug resistance patterns using disc diffusion, the phenotypic frequency of extended-spectrum beta-lactamase (ESBL)-producing isolates was measured by the double-disk synergy test (DDST) method. The isolates were examined for the presence of qnrA, qnrB, qnrS, and aac(6′)-Ib-cr genes by the polymerase chain reaction (PCR) assay. Results. The antibiotic resistance rate of E. cloacae isolates varied from 9.7% to 60.2%; among them, 78% were multidrug-resistant (MDR). The highest quinolone resistance was observed in ESBL-producing strains of E. cloacae. The frequency of positive isolates for PMQR and ESBL was 79.6% and 57.5%, respectively. The genes aac(6′)-ib-cr (70.8%) and qnrB (38.1%) had the highest frequency among other genes. The number of isolates simultaneously carrying 2 and 3 genes was 64 and 5 isolates, respectively. Conclusion. The obtained results indicate a high degree of quinolone resistance among ESBL-producing E. cloacae strains. Nevertheless, there was a significant relationship between the PMQR gene and ESBL-positive isolates. Therefore, special attention should be paid to molecular epidemiological studies on antibiotic resistance to quinolones and beta-lactamases in these strains.
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伊朗克尔曼沙阿临床标本中分离出的丁香肠杆菌菌株中质粒介导的喹诺酮抗性基因的丰富性
背景。泄殖腔肠杆菌(E. cloacae)是引起医院内感染的最常见肠杆菌科细菌之一。最近,人们开始考虑质粒介导的喹诺酮耐药性(PMQR)决定因素。本研究评估了从伊朗克尔曼沙阿(Kermanshah)临床样本中获得的丁香杆菌菌株中 PMQR 基因的丰度。研究方法在这项描述性横断面研究中,在收集了 113 株分离出的泄殖腔杆菌后,使用特定的生化测试确认了它们的身份。在使用盘扩散法确定其耐药性模式后,使用双盘协同试验(DDST)法测定了产生广谱β-内酰胺酶(ESBL)的分离物的表型频率。采用聚合酶链反应(PCR)检测分离物是否含有 qnrA、qnrB、qnrS 和 aac(6′)-Ib-cr 基因。结果衣褶杆菌分离株的抗生素耐药率从 9.7% 到 60.2% 不等,其中 78% 为多重耐药(MDR)。产生 ESBL 的衣藻埃希氏菌株对喹诺酮类药物的耐药性最高。PMQR和ESBL阳性分离株的比例分别为79.6%和57.5%。在其他基因中,aac(6′)-ib-cr(70.8%)和 qnrB(38.1%)基因的频率最高。同时携带 2 个和 3 个基因的分离物数量分别为 64 个和 5 个。结论研究结果表明,产 ESBL 的衣藻埃希氏菌株对喹诺酮类药物具有高度耐药性。然而,PMQR 基因与 ESBL 阳性分离物之间存在显著关系。因此,应特别关注对这些菌株的喹诺酮类抗生素耐药性和β-内酰胺酶的分子流行病学研究。
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