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Comparable Effect of Two-Step Versus Extended Infusions on the Pharmacokinetics of Imipenem in Patients with Sepsis and Septic Shock.两步输注与延长输注对脓毒症和感染性休克患者亚胺培南药代动力学的影响相当。
Adv Ther. 2020 May;37(5):2246-2255. doi: 10.1007/s12325-020-01339-5. Epub 2020 Apr 10.
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A review on bacterial resistance to carbapenems: epidemiology, detection and treatment options.碳青霉烯类抗生素的细菌耐药性综述:流行病学、检测及治疗选择
Future Sci OA. 2020 Jan 27;6(3):FSO438. doi: 10.2144/fsoa-2019-0098.
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Epidemiology of colistin-resistant, carbapenemase-producing Enterobacteriaceae and Acinetobacter baumannii in Croatia.克罗地亚产碳青霉烯酶、耐药黏菌素肠杆菌科和鲍曼不动杆菌的流行病学研究。
Infect Genet Evol. 2020 Jul;81:104263. doi: 10.1016/j.meegid.2020.104263. Epub 2020 Feb 24.
4
Carbapenem-Sparing Strategies for ESBL Producers: When and How.针对产超广谱β-内酰胺酶(ESBL)菌的碳青霉烯类抗菌药物节省策略:时机与方法
Antibiotics (Basel). 2020 Feb 5;9(2):61. doi: 10.3390/antibiotics9020061.
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Clinical pharmacokinetics of 3-h extended infusion of meropenem in adult patients with severe sepsis and septic shock: implications for empirical therapy against Gram-negative bacteria.美罗培南3小时延长输注在严重脓毒症和脓毒性休克成年患者中的临床药代动力学:对革兰氏阴性菌经验性治疗的意义
Ann Intensive Care. 2020 Jan 10;10(1):4. doi: 10.1186/s13613-019-0622-8.
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Carbapenem-Resistant : Microbiology Key Points for Clinical Practice.耐碳青霉烯类:临床实践的微生物学要点
Int J Gen Med. 2019 Nov 28;12:437-446. doi: 10.2147/IJGM.S214305. eCollection 2019.
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Tigecycline-non-susceptible hypervirulent Klebsiella pneumoniae strains in Taiwan.台湾地区对替加环素不敏感的高毒力肺炎克雷伯菌。
J Antimicrob Chemother. 2020 Feb 1;75(2):309-317. doi: 10.1093/jac/dkz450.
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Molecular Epidemiology of Multidrug-Resistant Isolates in a Brazilian Tertiary Hospital.巴西一家三级医院耐多药分离株的分子流行病学
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Epidemic of carbapenem-resistant Klebsiella pneumoniae in Europe is driven by nosocomial spread.欧洲耐碳青霉烯类肺炎克雷伯菌的流行是由医院内传播驱动的。
Nat Microbiol. 2019 Nov;4(11):1919-1929. doi: 10.1038/s41564-019-0492-8. Epub 2019 Jul 29.
10
The Efficacy and Safety of Doripenem in the Treatment of Acute Bacterial Infections-A Systemic Review and Meta-Analysis of Randomized Controlled Trials.多利培南治疗急性细菌感染的疗效与安全性——随机对照试验的系统评价与Meta分析
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耐厄他培南、碳青霉烯酶阴性且孔蛋白缺陷的产超广谱β-内酰胺酶菌的暴发。

An outbreak of ertapenem-resistant, carbapenemase-negative and porin-deficient ESBL-producing complex.

作者信息

Matovina Mihaela, Abram Maja, Repac-Antić Davorka, Knežević Samira, Bubonja-Šonje Marina

机构信息

PhD, Division of Organic Chemistry and Biochemistry, Rudjer Bošković Institute, Bijenička cesta 54, 10 000 Zagreb, Croatia.

MD, PhD, Department of Microbiology, Faculty of Medicine, University of Rijeka, Braće Branchetta 20, 51 000 Rijeka, Croatia and Department of Clinical Microbiology, Clinical Hospital Center Rijeka, Krešimirova 40, 51 000 Rijeka, Croatia.

出版信息

Germs. 2021 Jun 2;11(2):199-210. doi: 10.18683/germs.2021.1257. eCollection 2021 Jun.

DOI:10.18683/germs.2021.1257
PMID:34422692
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8373410/
Abstract

INTRODUCTION

Carbapenem-resistant is an emerging healthcare-associated pathogen with dynamic molecular epidemiology. This study presents a retrospective analysis of the distribution and antibiotic resistance patterns of ertapenem-resistant ESBL-producing strains recovered during an outbreak from 2012 to 2014 in a Croatian University hospital.

METHODS

We aimed to estimate genetic relatedness of clinical isolates and underlying mechanisms that conferred the ertapenem-resistant phenotype.

RESULTS

Expression analysis of genes involved in the antibiotic resistance showed reduced expression of major non-selective porin channel OmpK35. Reduced expression of OmpK36 porin channel in isolates resistant to at least one more carbapenem, apart from the ertapenem, was found to a lesser degree. Pulsed-field gel electrophoresis analysis of genomic DNA revealed that almost all isolates belonged to the same genetic clone.

CONCLUSIONS

Caution regarding ertapenem-resistant, carbapenemase-negative porin-deficient mutants of is required as they are widespread, and under selective pressure this could result in a local clonal outbreak.

摘要

引言

耐碳青霉烯类肠杆菌科细菌是一种新出现的与医疗保健相关的病原体,其分子流行病学动态变化。本研究对2012年至2014年克罗地亚一家大学医院暴发期间分离出的产超广谱β-内酰胺酶(ESBL)且耐厄他培南的菌株的分布及抗生素耐药模式进行了回顾性分析。

方法

我们旨在评估临床分离株的遗传相关性以及赋予耐厄他培南表型的潜在机制。

结果

参与抗生素耐药的基因表达分析显示,主要的非选择性孔蛋白通道OmpK35表达降低。在除厄他培南外还对至少一种其他碳青霉烯类耐药的分离株中,OmpK36孔蛋白通道表达降低的程度较小。基因组DNA的脉冲场凝胶电泳分析表明,几乎所有分离株都属于同一遗传克隆。

结论

对于耐厄他培南、碳青霉烯酶阴性且孔蛋白缺陷的肠杆菌科细菌突变体需谨慎对待,因为它们广泛存在,在选择性压力下可能导致局部克隆性暴发。