Molecular characterization of resistance and biofilm genes of ESKAPE pathogens isolated from clinical samples: examination of the effect of boric acid on biofilm ability by cell culture method.

IF 4.2 2区 生物学 Q2 MICROBIOLOGY BMC Microbiology Pub Date : 2025-03-01 DOI:10.1186/s12866-025-03830-x
Ozgur Celebi, Sumeyye Baser, Mustafa Can Guler, Ali Taghizadehghalehjoughi, Erva Rakici, Elif Aydin, Demet Celebi
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Abstract

Biofilm formation ranks first among the resistance and virulence factors crucial in forming ESKAPE pathogens. Once biofilm is formed, treating the infection with existing drugs is often futile. Therefore, in this study, resistant ESKAPE pathogens were isolated from intensive care units and sent to Atatürk University Yakutiye Research Hospital Microbiology Laboratory. This study investigated the biofilm formation and molecular characterization of resistant ESKAPE pathogens isolated from intensive care units. The bacteria's biofilm formation abilities, genes responsible for biofilm formation, and resistance characteristics were identified. The effect of boric acid (BA) on resistance and bacterial genes was evaluated by a bacterial infection cell culture model. The highest biofilm formation was observed in Escherichia coli, Enterococcus spp., and Pseudomonas aeruginosa Enterococcus spp. isolates showed the vanA gene in 14.6% and the vanC gene in 61% of the samples. Among Staphylococcus spp. isolates, 48.3% were MSSA, 34.5% were MRCNS, and 17.2% were MRSA. The KPC gene was detected in 50%, the OXA-48 gene in 40%, and the NDM gene in 15% of the isolates. In P. aeruginosa, the LasI and LasR quorum sensing system genes were found in 38.5% and 30.8% of the isolates, respectively. In E. coli isolates, OXA-48 was present in 35%, KPC in 31.7%, and TEM in 12.5%. BA demonstrated significant activity against ESKAPE pathogens. The combined antimicrobial activity of boron compounds showed a decrease in the expression level of the resistance gene. It will be promising for preventing hospital-associated infections.

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从临床样本中分离出的 ESKAPE 病原体的抗药性和生物膜基因的分子特征:通过细胞培养法研究硼酸对生物膜能力的影响。
在形成ESKAPE病原菌的关键耐药和毒力因素中,生物膜的形成排在第一位。一旦生物膜形成,用现有的药物治疗感染往往是无效的。因此,在本研究中,从重症监护病房分离出耐药ESKAPE病原体,并送到atatatrk大学雅库特耶研究医院微生物实验室。本研究调查了从重症监护病房分离的耐药ESKAPE病原体的生物膜形成和分子特征。鉴定了细菌的生物膜形成能力、生物膜形成的基因和抗性特征。采用细菌感染细胞培养模型,研究了硼酸(BA)对细菌抗性和细菌基因的影响。大肠埃希菌、肠球菌和铜绿假单胞菌的生物膜形成率最高,其中14.6%的样品含有vanA基因,61%的样品含有vanC基因。葡萄球菌分离株中MSSA 48.3%, MRCNS 34.5%, MRSA 17.2%。50%的分离株检出KPC基因,40%检出OXA-48基因,15%检出NDM基因。在铜绿假单胞菌中,分别有38.5%和30.8%的菌株含有LasI和LasR群体感应系统基因。在大肠杆菌分离株中,OXA-48占35%,KPC占31.7%,TEM占12.5%。BA对ESKAPE病原菌有明显的抑制作用。硼化合物的联合抑菌活性降低了抗性基因的表达水平。它将有望预防医院相关感染。
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来源期刊
BMC Microbiology
BMC Microbiology 生物-微生物学
CiteScore
7.20
自引率
0.00%
发文量
280
审稿时长
3 months
期刊介绍: BMC Microbiology is an open access, peer-reviewed journal that considers articles on analytical and functional studies of prokaryotic and eukaryotic microorganisms, viruses and small parasites, as well as host and therapeutic responses to them and their interaction with the environment.
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