Golikova Maria V, Alieva Kamilla N, Strukova Elena N, Kondratieva Daria A, Petrova Nika F, Petrova Mayya A, Zinner Stephen H
Department of Pharmacokinetics & Pharmacodynamics, Gause Institute of New Antibiotics, 11 Bolshaya Pirogovskaya Street, 119021 Moscow, Russia.
National Research Centre "Kurchatov Institute", 123182 Moscow, Russia.
Antibiotics (Basel). 2023 Dec 12;12(12):1717. doi: 10.3390/antibiotics12121717.
Resistance to carbapenems has become a problem due to (), harboring carbapenemases. Among them, there are isolates that are recognized as carbapenem-susceptible; however, these carbapenemase-producing strains with low meropenem minimal inhibitory concentrations (MICs) may pose a threat to public health. We aimed to investigate the impact of the ability to produce carbapenemases by a bacterial isolate on the effectiveness of meropenem in the hollow-fiber infection model. and () strains with equal meropenem MICs but differing in their ability to produce carbapenemases were used in pharmacodynamic simulations with meropenem. In addition to standard MIC determination, we assessed the MICs against tested strains at high inoculum density to test if the inoculum effect occurs. According to pharmacodynamic data, the carbapenemase-producing strains were characterized with a relatively decreased meropenem effectiveness compared to non-producers. Meanwhile, the effect of meropenem perfectly correlated with the meropenem exposure expressed as the DOSE/MIC ratio when high-inoculum (HI) MICs but not standard-inoculum (SI) MICs were used for regression analysis. It could be concluded that meropenem-susceptible carbapenemase-producing strains may not respond to meropenem therapy; the antibiotic inoculum effect (IE) may have a prognostic value to reveal the meropenem-susceptible that harbor carbapenemase genes.
由于()携带碳青霉烯酶,对碳青霉烯类药物的耐药性已成为一个问题。其中,有些分离株被认为对碳青霉烯类药物敏感;然而,这些美罗培南最低抑菌浓度(MIC)较低的产碳青霉烯酶菌株可能对公众健康构成威胁。我们旨在研究细菌分离株产生碳青霉烯酶的能力对中空纤维感染模型中美罗培南有效性的影响。使用美罗培南MIC相同但产碳青霉烯酶能力不同的()菌株进行美罗培南的药效学模拟。除了标准的MIC测定外,我们还评估了高接种量密度下受试菌株的MIC,以测试是否存在接种量效应。根据药效学数据,与非产酶菌株相比,产碳青霉烯酶菌株的美罗培南有效性相对降低。同时,当使用高接种量(HI)MIC而非标准接种量(SI)MIC进行回归分析时,美罗培南的效应与以DOSE/MIC比值表示的美罗培南暴露量完美相关。可以得出结论,对美罗培南敏感的产碳青霉烯酶菌株可能对美罗培南治疗无反应;抗生素接种量效应(IE)可能具有预后价值,以揭示携带碳青霉烯酶基因的对美罗培南敏感的()。