Department of Molecular and Cellular Biology, University of Guelphgrid.34429.38, Guelph, Ontario, Canada.
Institut de Biologie Integrative et des Systems (IBIS), Département de Microbiologie-Infectiologie et d'Immunologie, Université Laval, Laval, Quebec, Canada.
Microbiol Spectr. 2022 Jun 29;10(3):e0102422. doi: 10.1128/spectrum.01024-22. Epub 2022 Jun 6.
Eight isolates of the Liverpool epidemic strain (LES) of Pseudomonas aeruginosa have previously been characterized using comparative genomics and preliminary phenotypic assays. Here, we extend the characterization of these clinically relevant P. aeruginosa isolates with planktonic and biofilm growth assays and analysis of antibiotic susceptibility for both planktonic and biofilm cultures. Laboratory strains PAO1 and PA14 were included as comparator strains. Antibiotic susceptibility to eight classes of antibiotics was determined. MICs were determined to measure susceptibility of planktonic cultures, and minimum biofilm eradication concentration (MBEC) assays were used to estimate levels of resistance during the production of biofilm. LES isolates had high levels of resistance compared with laboratory reference strains when grown planktonically (up to nine 2-fold dilutions higher), and resistance was increased in the biofilm mode of growth. Measurements of biofilm biomass in the MBEC assays showed that certain isolates often show increased biofilm biomass in the presence of antibiotics. Pseudomonas aeruginosa is an opportunistic pathogen with high intrinsic antibiotic resistance. This resistance is typically increased in clinical isolates through adaptations to the host and production of small-colony variants (SCVs) and when P. aeruginosa forms biofilms, which are surface-attached communities that are protected by a self-produced matrix. Understanding the combination of SCVs, biofilm production, and the diversity of drug resistance phenotypes in clinical isolates can lead to improved treatments for P. aeruginosa infections.
先前,我们使用比较基因组学和初步表型分析对来自利物浦流行株(LES)的 8 株铜绿假单胞菌进行了特征描述。在这里,我们通过浮游和生物膜生长试验以及浮游和生物膜培养物抗生素敏感性分析,对这些具有临床相关性的铜绿假单胞菌分离株进行了进一步的特征描述。实验室菌株 PAO1 和 PA14 被用作比较菌株。测定了 8 类抗生素的药敏性。测定 MIC 以测量浮游培养物的敏感性,并且使用最低生物膜清除浓度(MBEC)测定来估计生物膜形成过程中的耐药水平。与实验室参考菌株相比,LES 分离株在浮游生长时具有更高水平的耐药性(高达 9 倍的 2 倍稀释度),并且在生物膜生长模式下耐药性增加。MBEC 测定中的生物膜生物量测量表明,某些分离株在存在抗生素时通常会显示出增加的生物膜生物量。铜绿假单胞菌是一种机会性病原体,具有很高的固有抗生素耐药性。这种耐药性通常通过适应宿主和产生小菌落变体(SCV)以及当铜绿假单胞菌形成生物膜时增加,生物膜是由自身产生的基质保护的表面附着群落。了解 SCV、生物膜产生以及临床分离株中药物耐药表型的多样性的组合可以导致改善铜绿假单胞菌感染的治疗方法。