Silva Vanessa, Correia Elisete, Pereira José Eduardo, González-Machado Camino, Capita Rosa, Alonso-Calleja Carlos, Igrejas Gilberto, Poeta Patrícia
Microbiology and Antibiotic Resistance Team (MicroART), Department of Veterinary Sciences, University of Trás-os-Montes and Alto Douro (UTAD), 5000-801 Vila Real, Portugal.
Department of Genetics and Biotechnology, University of Trás-os-Montes and Alto Douro (UTAD), 5000-801 Vila Real, Portugal.
Antibiotics (Basel). 2022 Jun 4;11(6):772. doi: 10.3390/antibiotics11060772.
This study aimed to compare the biofilm formation ability of isolated from a wide range of animals and study the association between biofilm formation and antimicrobial resistance and genetic lineages. A total of 214 strains isolated from pets, livestock, and wild animals were evaluated regarding their ability to form biofilms by the microtiter biofilm assay and their structure via confocal scanning laser microscopy. Statistical analysis was used to find an association between biofilm formation and antimicrobial resistance, multidrug resistance, sequence types (STs), and -types of the isolates. The antimicrobial susceptibility of 24 h-old biofilms was assessed against minimum inhibitory concentrations (MIC) and 10× MIC of amikacin and tetracycline, and the biomass reduction was measured. The metabolic activity of biofilms after antimicrobial treatment was evaluated by the XTT assay. All isolates were had the ability to form biofilms. Yet, significant differences in biofilm biomass production were detected among animal species. Multidrug resistance had a positive association with biofilm formation as well as methicillin-resistance. Significant differences were also detected among the clonal lineages of the isolates. Both tetracycline and amikacin were able to significantly reduce the biofilm mass. However, none of the antimicrobials were able to eradicate the biofilm at the maximum concentration used. Our results provide important information on the biofilm-forming capacity of animal-adapted isolates, which may have potential implications for the development of new biofilm-targeted therapeutics.
本研究旨在比较从多种动物中分离出的[具体内容缺失]的生物膜形成能力,并研究生物膜形成与抗菌药物耐药性及遗传谱系之间的关联。通过微量滴定板生物膜检测法评估了从宠物、家畜和野生动物中分离出的214株菌株形成生物膜的能力,并利用共聚焦扫描激光显微镜观察了其结构。采用统计分析方法来寻找生物膜形成与抗菌药物耐药性、多重耐药性、序列类型(STs)以及分离株的[具体内容缺失]类型之间的关联。针对阿米卡星和四环素的最低抑菌浓度(MIC)以及10倍MIC,评估了24小时龄生物膜的抗菌药物敏感性,并测定了生物量减少情况。通过XTT检测法评估了抗菌治疗后生物膜的代谢活性。所有分离株均具有形成生物膜的能力。然而,在动物物种之间检测到生物膜生物量产生存在显著差异。多重耐药性与生物膜形成以及耐甲氧西林性呈正相关。在分离株的克隆谱系之间也检测到了显著差异。四环素和阿米卡星均能够显著降低生物膜质量。然而,在所使用的最大浓度下,没有一种抗菌药物能够根除生物膜。我们的结果提供了关于适应动物的[具体内容缺失]分离株生物膜形成能力的重要信息,这可能对开发新的针对生物膜的治疗方法具有潜在意义。