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苏丹喀土穆产碳青霉烯酶的GIM-1和SIM-1临床分离株的出现

The Emergence of Carbapenem Resistant Producing GIM-1 and SIM-1 Clinical Isolates in Khartoum-Sudan.

作者信息

Bayoumi Magdi A, Hamid Omnia M

机构信息

Medical Microbiology-Faculty of Medicine, University of Medical Sciences& Technology-UMST Khartoum, Khartoum, Sudan.

Medical Microbiology-Faculty of Medical Laboratory Sciences, University of Medical Sciences& Technology-UMST, Khartoum, Sudan.

出版信息

Infect Drug Resist. 2022 May 25;15:2679-2684. doi: 10.2147/IDR.S365983. eCollection 2022.

Abstract

PURPOSE

The aim of this study was to detect multidrug resistant GIM-1 and SIM-1 producing clinical isolates from hospitalized patients across three Khartoum State Teaching Hospitals, Sudan.

PATIENTS AND METHODS

From May 2018 to October 2019, clinical isolates from inpatients admitted to different Khartoum state hospitals. Genes for carbapenemase (GIM-1 and SIM-1) were amplified by polymerase chain reaction (PCR). Agar dilution method was used to determine MICs for imipenem and meropenem after antimicrobial susceptibility testing.

RESULTS

Five (1.29%) isolates of [2 (0.51%) isolates produce GIM-1, 2 (0.51%) isolates (one [0.25%] of each produce of GIM-1 and of SIM-1), and 1 (0.25%) isolate produce GIM-1]. Susceptibility profiling of the isolates showed a low-level resistance to imipenem and meropenem MICs (8, 16 and 32 μg/mL). It also had resistance to ampicillin, extended-spectrum cephalosporin's, aztreonam, and amoxicillin-clavulanate and with the two strains showing resistance to colistin.

CONCLUSION

We report the emergence of four GIM-1 producing strains and one strain of SIM-1 producing genes, isolated from hospitalized patients, with a high resistance pattern to antimicrobial agents. Whole-genome sequencing (WGS) is necessary for precise identification of clonal diversity backgrounds of acquired carbapenemase genes in diagnostic laboratories as the number of cases of carbapenem resistant infection increases annually.

摘要

目的

本研究旨在从苏丹喀土穆州的三家教学医院的住院患者中检测产多药耐药GIM-1和SIM-1的临床分离株。

患者与方法

2018年5月至2019年10月,收集喀土穆州不同医院住院患者的临床分离株。采用聚合酶链反应(PCR)扩增碳青霉烯酶(GIM-1和SIM-1)基因。抗菌药物敏感性试验后,采用琼脂稀释法测定亚胺培南和美罗培南的最低抑菌浓度(MIC)。

结果

5株(1.29%)分离株[2株(0.51%)产GIM-1,2株(0.51%)(各有1株(0.25%)产GIM-1和SIM-1),1株(0.25%)产GIM-1]。分离株的药敏谱显示对亚胺培南和美罗培南MIC呈低水平耐药(8、16和32μg/mL)。它还对氨苄西林、超广谱头孢菌素、氨曲南和阿莫西林-克拉维酸耐药,其中两株对黏菌素耐药。

结论

我们报告了从住院患者中分离出4株产GIM-1菌株和1株产SIM-1基因的菌株,它们对抗菌药物具有高度耐药模式。随着碳青霉烯耐药感染病例数逐年增加,在诊断实验室中,全基因组测序(WGS)对于准确鉴定获得性碳青霉烯酶基因的克隆多样性背景是必要的。

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