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广宿主范围肽核酸可预防与导管相关的尿路感染中涉及的革兰氏阴性菌生物膜。

Broad Host Range Peptide Nucleic Acids Prevent Gram-Negative Biofilms Implicated in Catheter-Associated Urinary Tract Infections.

作者信息

Karp Hannah Q, Nowak Elizabeth S, Kropp Gillian A, Col Nihan A, Schulz Michael D, Sriranganathan Nammalwar, Rao Jayasimha

机构信息

Virginia Tech Carilion School of Medicine, Roanoke, VA 24016, USA.

Carilion Clinic Department of Infectious Disease, Carilion Clinic, Roanoke, VA 24014, USA.

出版信息

Microorganisms. 2025 Aug 20;13(8):1948. doi: 10.3390/microorganisms13081948.

Abstract

Biofilms develop in sequential steps resulting in the formation of three-dimensional communities of microorganisms that are encased in self-produced extracellular polymeric substances. Biofilms play a key role in device-associated infections, such as catheter-associated urinary tract infections (CAUTIs), because they protect microorganisms from standard antimicrobial therapies. Current strategies to prevent biofilm formation in catheter-related infections, including prophylactic antibiotics and antibiotic-coated catheters, have been unsuccessful. This finding highlights a need for novel approaches to address this clinical problem. In this study, biofilm-forming phenotypes of common Gram-negative bacteria associated with CAUTIs were treated with antisense peptide nucleic acids (PNAs), and biofilm biomass and bacterial viability were quantified after 24 h of treatment. A cocktail of PNAs targeting the global regulator genes , , and in significantly reduced viability and thus appropriately eliminated biofilm biomass. Antisense-PNAs against these same gene targets and the motility regulator gene inhibited biofilm formation among isolates of , , and but did not reduce bacterial viability. These results suggest that antisense-PNAs are a promising new technology in preventing biofilm formation in urinary catheters, especially as a potential complement to conventional antimicrobials.

摘要

生物膜按顺序逐步形成,导致微生物形成三维群落,这些群落被自身产生的细胞外聚合物包裹。生物膜在与器械相关的感染中起关键作用,如导管相关的尿路感染(CAUTIs),因为它们能保护微生物免受标准抗菌治疗。目前预防导管相关感染中生物膜形成的策略,包括预防性使用抗生素和抗生素涂层导管,均未成功。这一发现凸显了需要新方法来解决这一临床问题。在本研究中,用反义肽核酸(PNA)处理与CAUTIs相关的常见革兰氏阴性菌的生物膜形成表型,并在处理24小时后对生物膜生物量和细菌活力进行定量。针对大肠杆菌中全局调节基因、和的PNA混合物显著降低了活力,从而适当消除了生物膜生物量。针对相同基因靶点和运动调节基因的反义PNA抑制了大肠杆菌、肺炎克雷伯菌和铜绿假单胞菌分离株中的生物膜形成,但未降低细菌活力。这些结果表明,反义PNA是预防导尿管生物膜形成的一种有前景的新技术,尤其是作为传统抗菌药物的潜在补充。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5d5/12388306/e298ccde57dc/microorganisms-13-01948-g0A1.jpg

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