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生物膜中抗菌药物敏感性测定的创新方法

Innovative Methodology for Antimicrobial Susceptibility Determination in Biofilms.

作者信息

Jacobson B Tegner, DeWit-Dibbert Jessica, Selong Eli T, Quirk McKenna, Throolin Michael, Corona Chris, Sonar Sobha, Zanca LaShae, Schwarz Erika R, Bimczok Diane

机构信息

Department of Microbiology and Cell Biology, Montana State University, Bozeman, MT 59718, USA.

Department of Chemistry and Biochemistry, Montana State University, Bozeman, MT 59718, USA.

出版信息

Microorganisms. 2024 Dec 20;12(12):2650. doi: 10.3390/microorganisms12122650.

Abstract

spp. are facultative pathogens that contribute to the pathogenesis of multiple bovine diseases, including the bovine respiratory disease complex, and have been shown to form biofilms. Biofilm formation is associated with increased antibiotic resistance in many organisms, but accurate determination of antimicrobial susceptibility in biofilms is challenging. In spp., antimicrobial susceptibility is routinely determined using metabolic pH-dependent color change. However, biofilm formation can lead to reduced metabolism, making interpretation of metabolic readouts difficult. Therefore, we developed and optimized a new flow cytometry-based method for antimicrobial susceptibility testing in biofilm-forming , termed the live/dead antimicrobial susceptibility test (LD-AST). The LD-AST measures the proportion of live bacteria upon exposure to antibiotics, works robustly with both planktonic and biofilm cultures, and enables the determination of the minimum bactericidal concentration (MBC) for a given antibiotic. We used two strains of (Donetta PG45 and Madison) and two clinical isolates (MVDL1 and MVDL2) to determine the impact of biofilm growth on antimicrobial susceptibility for gentamicin, enrofloxacin, or tetracycline. All strains were susceptible to all antibiotics when cultured as planktonic cells, with MBCs in the expected range. However, three out of four strains (Donetta PG45, MVDL1, and MVDL2) were completely resistant to all three antibiotics when newly adhered biofilms were analyzed, whereas Madison gave variable results. For mature biofilms that were cultured for 4-5 days before antibiotic exposure, results also were variable, with some strains showing an increased resistance with certain antibiotics and a decreased resistance with others. Overall, these results are consistent with earlier reports that biofilms can exhibit increased antimicrobial resistance.

摘要

[该菌]属兼性病原菌,可引发多种牛类疾病,包括牛呼吸道疾病综合征,且已证实其能形成生物被膜。生物被膜的形成与许多生物体抗生素耐药性增加有关,但准确测定生物被膜中的抗菌药敏性具有挑战性。在[该菌]属中,通常利用代谢pH依赖性颜色变化来测定抗菌药敏性。然而,生物被膜的形成会导致代谢降低,使得代谢读数的解读变得困难。因此,我们开发并优化了一种基于流式细胞术的新方法,用于检测形成生物被膜的[该菌]的抗菌药敏性,称为活菌/死菌抗菌药敏试验(LD-AST)。LD-AST可测量暴露于抗生素后活菌的比例,对浮游菌和生物被膜培养物均能有效检测,并能确定给定抗生素的最低杀菌浓度(MBC)。我们使用了两株[该菌](多内塔PG45和麦迪逊)以及两株临床[该菌]分离株(MVDL1和MVDL2)来确定生物被膜生长对庆大霉素、恩诺沙星或四环素抗菌药敏性的影响。所有[该菌]菌株作为浮游细胞培养时对所有抗生素均敏感,MBC在预期范围内。然而,在分析新附着的生物被膜时,四株菌株中有三株(多内塔PG45、MVDL1和MVDL2)对所有三种抗生素完全耐药,而麦迪逊菌株的结果则各不相同。对于在接触抗生素前培养4 - 5天的成熟生物被膜,结果也各不相同,一些菌株对某些抗生素的耐药性增加,而对其他抗生素的耐药性降低。总体而言,这些结果与早期关于生物被膜可表现出增加的抗菌耐药性的报道一致。

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