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针对达巴万星接种物效应:辅助单剂量达托霉素

Targeting Dalbavancin Inoculum Effect: Adjunctive Single Dose of Daptomycin.

作者信息

Kebriaei Razieh, Abdul-Mutakabbir Jacinda C, Stamper Kyle C, Lev Katherine L, Rybak Michael J

机构信息

Department of Pharmacy Practice, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, Detroit, MI, USA.

P3 Research Laboratory, Division of Outcomes and Translational Sciences, College of Pharmacy, Ohio State University, Columbus, USA.

出版信息

Infect Dis Ther. 2023 Oct;12(10):2485-2494. doi: 10.1007/s40121-023-00875-1. Epub 2023 Oct 5.

Abstract

INTRODUCTION

Daptomycin (DAP) has proven to be a viable alternative amid vancomycin resistance; however, the use of DAP post vancomycin treatment has led to the development of DAP non-susceptible (DNS) strains. Dalbavancin (DAL), a novel single-dosed lipoglycopeptide, has shown enhanced activity against highly resistant Staphylococcus aureus strains. However, on the basis of previous reports and our observations, DAL does not demonstrate similar activity at high versus low inoculum levels. Therefore, we hypothesized that addition of DAP even at minimal concentrations (single dose on day 1) will lower the inoculum to the level that can be cleared by dalbavancin.

METHODS

Isolates from methicillin-resistant S. aureus (MRSA)-infected patients with varying susceptibility profiles were evaluated using broth microdilution methods. Two DNS-VISA strains (vancomycin intermediate resistant S. aureus) and one MRSA strain were further evaluated in a one-compartment PK/PD model using a high starting initial inoculum of 10 CFU/mL as well as low initial inoculum of 10 CFU/mL over 168 h to assess the activity of DAL and DAP monotherapy and in combination.

RESULTS

Single therapies were not bactericidal when evaluated in the 168 h in vitro one-compartment model with an initial inoculum of 10; however, the combination of DAL plus single dose of DAP resulted in enhanced killing at the end of the 168-h exposure. DAL single therapy caused reduction in colony counts down to detection limit (2 log CFU/ml) at a lower inoculum but did not show enhancement (< 2 log CFU/ml) at higher initial inoculums (P < 0.01) for all three strains. Similarly, DAP caused initial bacterial reduction up to 4 log CFU/ml with regrowth at about 32 h of exposure, which stayed at initial inoculum levels for the duration of the model for all three strains.

CONCLUSIONS

Dalbavancin inoculum effect is a major issue in bacterial infections with high bacterial loads and the combination of DAL plus single dose of DAP showed promise in eradicating resistant S. aureus strains at high inoculums.

摘要

引言

达托霉素(DAP)已被证明是耐万古霉素情况下的一种可行替代药物;然而,在万古霉素治疗后使用达托霉素已导致出现对达托霉素不敏感(DNS)的菌株。达巴万星(DAL)是一种新型单剂量脂糖肽,已显示出对高度耐药金黄色葡萄球菌菌株增强的活性。然而,根据先前的报告和我们的观察,达巴万星在高接种量与低接种量水平下并未表现出类似的活性。因此,我们推测即使以最低浓度(第1天单剂量)添加达托霉素也会将接种量降低至达巴万星能够清除的水平。

方法

使用肉汤微量稀释法评估来自不同敏感性谱的耐甲氧西林金黄色葡萄球菌(MRSA)感染患者的分离株。使用10 CFU/mL的高起始初始接种量以及10 CFU/mL的低初始接种量在一室药代动力学/药效学模型中对两株DNS-VISA菌株(万古霉素中介耐药金黄色葡萄球菌)和一株MRSA菌株进行了168小时的进一步评估,以评估达巴万星和达托霉素单药治疗及联合治疗的活性。

结果

在初始接种量为10的168小时体外一室模型中评估时,单药治疗均无杀菌作用;然而,达巴万星加单剂量达托霉素的联合治疗在168小时暴露结束时导致杀菌增强。达巴万星单药治疗在较低接种量下使菌落计数降低至检测限(2 log CFU/ml),但在所有三株菌株的较高初始接种量下均未显示增强作用(<2 log CFU/ml)(P<0.01)。同样,达托霉素使细菌初始减少高达4 log CFU/ml,在暴露约32小时后重新生长,在模型持续时间内所有三株菌株的水平保持在初始接种量水平。

结论

达巴万星的接种量效应是高细菌载量细菌感染中的一个主要问题,达巴万星加单剂量达托霉素的联合治疗在根除高接种量下的耐药金黄色葡萄球菌菌株方面显示出前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdf6/10600059/00f8f3127615/40121_2023_875_Fig1_HTML.jpg

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