Laboratory of Microorganisms and Active Biomolecules, Department of Biology, Faculty of Sciences of Tunis, University of Tunis El Manar, Tunis, Tunisia.
Department of Infectious Diseases and Clinical Microbiology, İstanbul University-Cerrahpaşa, İstanbul, Turkey.
Microb Drug Resist. 2022 Jan;28(1):18-22. doi: 10.1089/mdr.2020.0417. Epub 2021 Aug 4.
has acquired resistance to several antimicrobial drugs, including last-resort antibiotics affecting, therefore, clinical efficacy and causing high rates of mortality. In this study, we investigate the whole genome sequence of a carbapenem-resistant strain isolated from the hospital environment in Tunisia. A total of 210 samples were taken using sterile swabs, from inanimate surfaces, medical devices, and care staff, during the period extended between March and April 2019. After the microbiological analysis of samples and antimicrobial susceptibility testing, only one strain identified as showing resistance to carbapenems was selected for the whole genome sequencing. The genome analysis revealed a high-level resistance to most antibiotics. Interestingly, we have noted the coexistence of and metallo-β-lactamase (MBL) encoding genes conferring resistance to carbapenems. Other β-lactamases encoding genes have also been detected, including , , and . Moreover, genes conferring resistance to aminoglycoside [(3)-IId, (3″)-Ia, A, (6')-Ib], macrolide [(A)], sulfonamide (1), trimethoprim (A1), tetracycline [(D)], chloramphenicol [(B3)], rifamycin (-3), and quinolone (B) have been revealed. The multi-locus sequence typing analysis showed that this isolate could not be assigned to an existing sequence type (ST), but it is almost identical to ST22. The plasmid investigation revealed the presence of five plasmids belonging to diverse incompatibility groups (IncFII, IncHI1A, IncHI1B, IncN, and IncX3). To the best of our knowledge, our findings report the first detection of NDM-1 and VIM-48 coproducing in Tunisia and the second detection in the world of the .
该菌已经对包括最后一线抗生素在内的多种抗菌药物产生了耐药性,从而影响了临床疗效,并导致高死亡率。在本研究中,我们对从突尼斯医院环境中分离的耐碳青霉烯肠杆菌进行了全基因组序列分析。2019 年 3 月至 4 月期间,我们使用无菌拭子从无生命表面、医疗器械和医护人员身上共采集了 210 个样本。对样本进行微生物分析和药敏试验后,仅选择了一株对碳青霉烯类药物表现出耐药性的 菌株进行全基因组测序。基因组分析显示,该菌对大多数抗生素均表现出高水平耐药性。有趣的是,我们注意到同时存在 和 编码基因,这些基因赋予了该菌对碳青霉烯类药物的耐药性。此外,还检测到了其他编码β-内酰胺酶的基因,包括 、 、和 。此外,还发现了赋予对氨基糖苷类 [(3)-IId、(3″)-Ia、A、(6')-Ib]、大环内酯类 [(A)]、磺胺类 (1)、甲氧苄啶 (A1)、四环素类 [(D)]、氯霉素 [(B3)]、利福霉素 (-3) 和喹诺酮类 (B)耐药的基因。多位点序列分型分析显示,该分离株无法归入现有的序列型 (ST),但与 ST22 几乎完全一致。质粒调查显示,存在属于不同不相容群 (IncFII、IncHI1A、IncHI1B、IncN 和 IncX3) 的 5 个质粒。据我们所知,我们的研究结果首次在突尼斯发现了同时产生 NDM-1 和 VIM-48 的 ,并且是世界上第二次发现 。