苏丹临床标本分离的耐多药肠杆菌的分子特征:缺乏SHV和TEM的CTX-M和碳青霉烯酶基因的流行

Hiba Abdel Salam Mahgoub, Hind Haidar Ahmed, Tyseer AbdelAzim Ahmed Mahgoub, Osama Mohammed Mohammed Khair, Mawada Hassan Fadlalla Mohammed, Maye Mohammed Merghani, Majdolin Ibrahim Mobark AlBushra, Elsadig Mohammed Hamdan, Rania Hashim MohammedKhair Khojli, Hisham Nour Aldaiem Altyab, Mogahid Mohammed Elhassan
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引用次数: 0

摘要

耐多药肠杆菌种类的增加是一个重大的全球卫生问题,特别是在医院环境中,它们会导致医院感染。本研究旨在确定苏丹喀土穆州临床标本中耐多药肠杆菌的流行情况,检测关键耐药基因(CTX-M、AmpC、OXA-48、NDM-1、VIM、IMP、MCR-1、SHV和TEM),并分析基因型和表型耐药模式的相关性。方法:于2021年2月至10月进行横断面实验室研究。从喀土穆的医院共收集了384份临床标本,包括尿液、伤口拭子、痰和血液。采用菌落形态学、革兰氏染色和生化试验等常规方法对分离的肠杆菌进行鉴定。采用Kirby-Bauer纸片扩散法进行药敏试验。采用多重聚合酶链反应(PCR)检测ESBL基因(CTX-M、SHV、TEM、AmpC)和碳青霉烯酶基因(OXA-48、NDM-1、VIM、IMP、MCR-1)。结果:384份临床标本中,经PCR鉴定为肠杆菌14例(3.6%)。所有分离株均表现出多药耐药。CTX-M基因100%检出,而SHV和TEM基因缺失。其他耐药基因包括AmpC 5株(35.7%)、IMP 2株(14.3%)、NDM-1 3株(21.4%)、VIM 5株(35.7%)、OXA-48 7株(50.0%)、MCR-1 13株(92.9%)。CTX-M、car-青霉烯酶基因的优势,以及SHV和TEM基因的缺失,表明这些分离株具有明显的耐药特征。讨论:研究结果强调了苏丹出现的耐多药肠杆菌,主要是由广泛存在的CTX-M和碳青霉烯酶基因驱动的。SHV和TEM基因的缺乏表明遗传抗性模式存在潜在的区域差异。这强调了分子监测和有效感染控制政策的迫切需要。结论:喀土穆地区耐多药肠杆菌的高流行率,特别是CTX-M和碳青霉烯酶基因的表达,对公共卫生构成严重威胁。耐药机制的区域差异,如缺乏SHV和TEM,需要有针对性的抗微生物药物管理和制定本地化治疗指南,以限制耐药性在苏丹卫生保健设施中的传播。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular Characterization of MDR Enterobacter spp. Isolated from Clinical Specimens in Sudan: Prevalence of CTX-M and Carbapenemase Genes with Absence of SHV and TEM.

Introduction: The rise of Multidrug-resistant (MDR) Enterobacter species is a significant global health concern, particularly in hospital settings where they contribute to nosocomial infections. This study aimed to determine the prevalence of MDR Enterobacter spp. in clinical specimens from Khartoum State, Sudan, to detect key resistance genes (CTX-M, AmpC, OXA-48, NDM-1, VIM, IMP, MCR-1, SHV, and TEM), and to analyze the correlation between genotypic and phenotypic resistance patterns.

Methods: A cross-sectional, laboratory-based study was conducted from February to October 2021. A total of 384 clinical specimens, including urine, wound swabs, sputum, and blood, were collected from hospitals in Khartoum. Enterobacter spp. isolates were identified using conventional methods such as colony morphology, Gram staining, and biochemical tests. Antimicrobial susceptibility testing was performed using the Kirby-Bauer disk diffusion method. Multiplex Polymerase Chain Reaction (PCR) was employed to detect ESBL genes (CTX-M, SHV, TEM, AmpC) and carbapenemase genes (OXA-48, NDM-1, VIM, IMP, MCR-1).

Results: Among the 384 clinical specimens, 14 (3.6%) were confirmed as Enterobacter spp. by PCR. All isolates exhibited multidrug resistance. CTX-M was detected in 100% of isolates, while SHV and TEM genes were absent. Other detected resistance genes included AmpC in 5 isolates (35.7%), IMP in 2 (14.3%), NDM-1 in 3 (21.4%), VIM in 5 (35.7%), OXA-48 in 7 (50.0%), and MCR-1 in 13 (92.9%). The predominance of CTX-M, car-bapenemase genes, and the absence of SHV and TEM suggest a distinct resistance profile in these isolates.

Discussion: The findings highlight a concerning emergence of MDR Enterobacter spp. in Sudan, primarily driven by the widespread presence of CTX-M and carbapenemase genes. The lack of SHV and TEM genes indicates potential regional differences in genetic resistance patterns. This underscores the critical need for molecular monitoring and effective infection control policies.

Conclusion: The high prevalence of MDR Enterobacter spp., particularly due to CTX-M and carbapenemase gene expression, poses a serious threat to public health in Khartoum. Regional variation in resistance mechanisms, such as the absence of SHV and TEM, necessitates targeted antimicrobial stewardship and the development of localized treatment guidelines to limit the spread of resistance in Sudanese healthcare facilities.

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