牛源大肠杆菌耐药基因的携带。

G Ozbey, E S Tanriverdi, M N Acik, R Kalin, B Otlu, F Zigo
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摘要

本研究旨在从2021年11月至2022年1月从东土耳其Bingol省12个私人牛场收集的240份新鲜粪便样本中分离出106株大肠杆菌(E. coli),寻找质粒介导的抗微生物药物耐药性基因的存在。在耐粘菌素大肠杆菌(mcr-1 ~ -9)中,利用多重聚合酶链式反应(PCR)方法和纳米孔技术新一代测序(NGS) - PCR扩增子,寻找主要的碳青霉烯酶(blaOXA-48、blaNDM-1、blaIMP、blaVIM和blaKPC)、β-内酰胺酶(blaem -1、blaCTX-M和blaSHV-1)和OXA-48样β-内酰胺酶(blaOXA-162、blaOXA-163、blaOXA-181、blaOXA-204和blaOXA-232)耐药基因。仅在一个分离株中发现了mcr-4基因,其余基因(mcr-1-9)未在所有牛大肠杆菌分离株中发现。采用肉汤微量稀释法检测mcr-4阳性大肠杆菌分离株对粘菌素的最低抑制浓度(MIC)。采用Kirby-Bauer圆盘扩散法对mcr-4阳性大肠杆菌分离株进行了抗菌药物敏感性评价。大肠杆菌碳青霉烯酶和OXA-48样β-内酰胺酶耐药基因均阴性,β-内酰胺酶阳性。此外,携带mcr-4的大肠杆菌分离株对粘菌素的耐药性更强。药敏试验结果表明,106株大肠杆菌(100%)对AMK敏感,105株(99.1%)对亚胺培南、美罗培南、多利培南敏感,1株(0.9%)对亚胺培南、美罗培南、多利培南耐药;所有菌株(100%)均对头孢噻肟耐药。大肠杆菌对氨苄西林(95.3%)、阿莫西林/克拉维酸(95.3%)、头孢吡肟(14.2%)、头孢克肟(19.8%)、头孢氨苄(74.5%)、庆大霉素(42.5%)、卡那霉素(37.7%)、链霉素(69.8%)、四环素(80.2%)、环丙沙星(60.4%)、诺氟沙星(13.2%)、氯霉素(59.4%)、甲氧苄啶/磺胺甲恶唑(68.9%)耐药。当我们研究Blast数据库中的序列时,大肠杆菌分离物的基因组显示与mcr-4序列高度相似。据我们所知,这是对土耳其牛大肠杆菌中mcr-4基因进行调查的第一份报告。我们的结果强调,牛可能是传播mcr基因的潜在风险。
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Carriage of antimicrobial resistance genes in Escherichia coli of bovine origin.

The present study aimed to search for the presence of the plasmid-mediated antimicrobial resistance genes in 106 Escherichia coli (E. coli) isolates from a total of 240 fresh fecal samples collected from 12 private cattle farms in Bingol province of East Turkey from November 2021 to January 2022. In those colistin-resistant E. coli (mcr-1 to -9), the major carbapenemase (blaOXA-48, blaNDM-1, blaIMP, blaVIM, and blaKPC), β-lactamase (blaTEM-1, blaCTX-M and blaSHV-1) and OXA-48 like β- lactamase (blaOXA-162, blaOXA-163, blaOXA-181, blaOXA-204 and blaOXA-232) resistance genes were searched for determined a multiplex polymerase chain reaction (PCR) method and Next-generation sequencing (NGS) - PCR Amplicons with Nanopore Technology. Only the mcr-4 gene was found in one isolate and the remaining genes (mcr-1-9) were not shown in all E. coli isolates from cattle. The minimal inhibitory concentration (MIC) to colistin was detected in mcr-4 positive E. coli isolates using broth microdilution. We assessed the antimicrobial susceptibilities of mcr-4 positive E. coli isolates using the Kirby-Bauer disk diffusion method. E coli isolate was detected as negative for carbapenemase and OXA-48 like β-lactamase resistance genes and positive for β-lactamase. In addition, E. coli isolates carrying mcr-4 were more resistant to colistin. Antimicrobial susceptibility testing using the disk diffusion assay indicated that all 106 E. coli isolates (100%) were sensitive to AMK, 105 E. coli isolates (99.1%) exhibited sensitivity to imipenem, meropenem and doripenem, and 1 E. coli isolate (0.9%) had intermediate resistance to imipenem, meropenem and doripenem; It was observed that all strains (100%) were resistant to cefotaxime. E. coli isolates are resistant to ampicillin (95.3%), amoxicillin/clavulanic acid (95.3%), cefepime (14.2%), cefixime (19.8%), cephalexin (74.5%), gentamicin (42.5%), kanamycin (37.7%), streptomycin (69.8%), tetracycline (80.2%), ciprofloxacin (60.4%), norfloxacin (13.2%), chloramphenicol (59.4%) and trimethoprim/sulfamethoxazole (68.9%). When we investigated the sequence in the Blast database, the genome of the E. coli isolate indicated high similarity with the mcr-4 sequences. To our knowledge, this is the first report investigating on the mcr-4 gene in E. coli identified from cattle in Turkey. Our results highlighted that cattle might be a potential risk in transmitting mcr genes.

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