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去铁酮和镓原卟啉有增强小菌落变异株中抗生素活性的能力。

Deferiprone and Gallium-Protoporphyrin Have the Capacity to Potentiate the Activity of Antibiotics in Small Colony Variants.

作者信息

Richter Katharina, Thomas Nicky, Zhang Guimin, Prestidge Clive A, Coenye Tom, Wormald Peter-John, Vreugde Sarah

机构信息

Department of Surgery, Otolaryngology Head and Neck Surgery, Basil Hetzel Institute for Translational Health Research, The Queen Elizabeth Hospital, University of AdelaideAdelaide, SA, Australia.

School of Pharmacy and Medical Sciences, University of South AustraliaAdelaide, SA, Australia.

出版信息

Front Cell Infect Microbiol. 2017 Jun 22;7:280. doi: 10.3389/fcimb.2017.00280. eCollection 2017.

Abstract

Small colony variants (SCVs) of bacteria like are characterized by a reduced colony size and are linked to increased antibiotic tolerance and resistance. Their altered expression of virulence factors, slow growing properties and their ability to form biofilms make the eradication of SCVs challenging. In the context of biofilm-related infectious diseases involving SCVs, a therapy targeting bacterial iron metabolism was evaluated. The combination of the iron-chelator deferiprone (Def) and the heme-analog gallium-protoporphyrin (GaPP), in solution and incorporated in a surgical wound gel, was tested for activity against planktonic and sessile SCVs. To this end, the activity of Def-GaPP was assessed against planktonic SCVs, as well as against and biofilms in the colony biofilm model, an artificial wound model and a infection model. While Def alone failed to show substantial antibacterial activity, GaPP and the combination of Def-GaPP demonstrated concentration- and strain-dependent antibacterial properties. Specifically, the Def-GaPP combination significantly reduced the bacterial load in an artificial wound model and increased the survival of SCV infected . When Def-GaPP were combined with gentamicin or ciprofloxacin, the triple combinations exceeded the antibiofilm activity of the individual compounds in the colony biofilm model. In targeting bacterial iron metabolism, Def-GaPP showed significant activity against planktonic and sessile SCVs. Moreover, Def-GaPP could potentiate the activity of gentamicin and ciprofloxacin. Delivered in a wound healing gel, Def-GaPP showed promise as a new topical strategy against infections with SCVs.

摘要

诸如[细菌名称]的细菌小菌落变异株(SCVs)的特征是菌落尺寸减小,并与抗生素耐受性和耐药性增加有关。它们毒力因子的表达改变、生长缓慢的特性以及形成生物膜的能力使得根除SCVs具有挑战性。在涉及SCVs的生物膜相关感染性疾病的背景下,评估了一种针对细菌铁代谢的疗法。测试了铁螯合剂去铁酮(Def)和血红素类似物镓原卟啉(GaPP)在溶液中以及掺入手术伤口凝胶中的组合对浮游和固着SCVs的活性。为此,评估了Def-GaPP对浮游SCVs以及在菌落生物膜模型、人工伤口模型和[感染模型名称]感染模型中对[细菌名称]生物膜的活性。虽然单独的Def未能显示出显著的抗菌活性,但GaPP以及Def-GaPP组合表现出浓度和菌株依赖性抗菌特性。具体而言,Def-GaPP组合在人工伤口模型中显著降低了细菌载量,并提高了感染SCV的[宿主名称]的存活率。当Def-GaPP与庆大霉素或环丙沙星联合使用时,三联组合在菌落生物膜模型中超过了各单一化合物的抗生物膜活性。在靶向细菌铁代谢方面,Def-GaPP对浮游和固着SCVs显示出显著活性。此外,Def-GaPP可以增强庆大霉素和环丙沙星的活性。以伤口愈合凝胶形式递送时,Def-GaPP有望成为一种针对SCVs感染的新型局部治疗策略。

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