首次报告来自巴勒斯坦加沙地带一家儿科医院的碳青霉烯类编码多重耐药革兰氏阴性菌。

IF 4 2区 生物学 Q2 MICROBIOLOGY
Nabil Abdullah El Aila, Nahed Ali Al Laham, Swapnil Prakash Doijad, Can Imirzalioglu, Mobarak Abu Mraheil
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引用次数: 0

摘要

背景:革兰氏阴性菌(GNB)中多重耐药性(MDR)在全球范围内的流行,特别是与广谱β-内酰胺酶(ESBLs)和碳青霉烯酶有关的耐药性,给全球公共卫生和临床带来了重大挑战:利用全基因组测序(WGS)分析加沙一家儿科医院内产 ESBL 的革兰氏阴性杆菌的特征:方法:从 Al-Nasser 儿科医院共收集了 158 株临床分离的革兰氏阴性杆菌。采用双盘协同试验检测了这些分离株是否产生 ESBL。根据临床和实验室标准研究所的指导方针,采用柯比鲍尔法确定抗生素敏感性谱。对选出的 15 个表型 MDR 分离物进行了全基因组测序,并对其基于基因组的物种特征和抗生素耐药基因谱进行了鉴定:结果:在 158 个分离株中,93 个(58.9%)对 ESBL 生产呈阳性反应。大肠埃希菌、肺炎克雷伯菌、铜绿假单胞菌、鲍曼不动杆菌、奇异变形杆菌和肉豆蔻沙雷氏菌的产生率分别为 50%、22.7%、22.7%、1.8%、1.2% 和 1.2%。尿液、脓液、血液和痰中的 ESBL 感染率分别为 64%、44%、23% 和 63.6%。氯霉素、亚胺培南和美罗培南是对 ESBL 生产者最有效的抗生素。在已测序的分离株中,每个分离株平均携带 6 个抗微生物耐药性(AMR)基因,其中一个分离株携带多达 13 个抗生素耐药性基因。检测到的碳青霉烯耐药基因包括 blaKPC-2(6.6%)、blaPDC-36/12(6.6%)和 blaPOM-1(6.6%)。所有测序的大肠埃希氏菌分离物(n = 8)均显示出多种耐药基因,主要是针对β-内酰胺酶(25.0%)、氨基糖苷类(37.5%)、磺胺类(37.5%)和四环素类(25.0)的耐药基因:我们的研究结果表明,从加沙地带一家儿科医院分离出的产 ESBL 的 GNB 感染率很高。我们发现了多种抗生素耐药基因,包括编码 ESBL 和碳青霉烯类的基因。研究结果突显了 GNB 中 MDR 带来的巨大挑战,并强调了有效抗生素策略的必要性。鉴于在巴勒斯坦的多项研究中观察到的高流行率,开展临床和分子流行病学研究以确定与携带 ESBL 和碳青霉烯耐药基因的 GNB 菌株相关的风险因素、传播模式和临床结果非常重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
First report of carbapenems encoding multidrug-resistant gram-negative bacteria from a pediatric hospital in Gaza Strip, Palestine.

Background: The worldwide prevalence of multi-drug resistance (MDR) in Gram-negative bacteria (GNB), particularly related to extended-spectrum beta-lactamases (ESBLs) and carbapenemases, poses significant global public health and clinical challenges.

Objectives: To characterize ESBL-producing Gram-negative bacilli, within a pediatric hospital in Gaza using whole genome sequencing (WGS).

Methods: A total of 158 clinical isolates of Gram-negative bacilli were collected from Al-Nasser Pediatric Hospital. These isolates were tested for ESBL production using the double disk synergy test. The antibiotic susceptibility profile was determined using the Kirby Bauer method following the Clinical and Laboratory Standard Institute guidelines. Selected 15 phenotypically MDR isolates were whole-genome sequenced and characterized for their genome-based species identity and antibiotic resistance gene profile.

Results: Of the 158 isolates, 93 (58.9%) were positive for ESBL production. The frequency of Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa, Acinetobacter baumannii, Proteus mirabilis, and Serratia marcescens was 50%, 22.7%, 22.7%, 1.8%, 1.2%, and 1.2% respectively. The prevalence of ESBL among urine, pus, blood, and sputum was 64%, 44%, 23%, and 63.6%, respectively. Chloramphenicol, Imipenem, and Meropenem were the most effective antibiotics against ESBL producers. In sequenced isolates,  an average of six anti-microbial resistance (AMR) genes were noted per isolate, where one of them carried up to 13 antibiotic resistance genes. Carbapenem resistance genes such as blaKPC-2(6.6%), blaPDC-36/12 (6.6%), and blaPOM-1 (6.6%) were detected. All the sequenced E. coli isolates (n = 8) showed multiple resistance genes, mainly against β-lactamase (25.0%), aminoglycosides (37.5%), sulfonamides (37.5%), and genes conferring resistance to tetracyclines (25.0).

Conclusion: Our results showed a high prevalence of ESBL-producing GNB isolated from a pediatric hospital in the Gaza Strip. Various antibiotic resistance genes were identified, including those encoding ESBL and carbapenems. The results highlight the significant challenge posed by MDR in GNB and emphasize the need for effective antibiotic strategies. Given the high endemicity observed in various studies from Palestine, it is important to conduct clinical and molecular epidemiology research to identify risk factors, transmission patterns, and clinical outcomes associated with GNB strains that carry ESBL and carbapenem resistance genes.

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来源期刊
BMC Microbiology
BMC Microbiology 生物-微生物学
CiteScore
7.20
自引率
0.00%
发文量
280
审稿时长
3 months
期刊介绍: BMC Microbiology is an open access, peer-reviewed journal that considers articles on analytical and functional studies of prokaryotic and eukaryotic microorganisms, viruses and small parasites, as well as host and therapeutic responses to them and their interaction with the environment.
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