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本文引用的文献

1
Aerosol phage therapy efficacy in Burkholderia cepacia complex respiratory infections.气溶胶噬菌体疗法在洋葱伯克霍尔德菌复合体呼吸道感染中的疗效
Antimicrob Agents Chemother. 2014 Jul;58(7):4005-13. doi: 10.1128/AAC.02388-13. Epub 2014 May 5.
2
Genomic characterization of JG068, a novel virulent podovirus active against Burkholderia cenocepacia.新型针对洋葱伯克霍尔德菌的毒力短小噬菌体 JG068 的基因组特征。
BMC Genomics. 2013 Aug 27;14:574. doi: 10.1186/1471-2164-14-574.
3
Burkholderia pseudomultivorans sp. nov., a novel Burkholderia cepacia complex species from human respiratory samples and the rhizosphere.伯克霍尔德氏菌假多样亚种,一种新型洋葱伯克霍尔德氏菌复合群物种,分离自人类呼吸道样本和根际。
Syst Appl Microbiol. 2013 Oct;36(7):483-9. doi: 10.1016/j.syapm.2013.06.003. Epub 2013 Jul 16.
4
Key role for efflux in the preservative susceptibility and adaptive resistance of Burkholderia cepacia complex bacteria.外排泵在洋葱伯克霍尔德菌复合群细菌的防腐剂敏感性和适应性耐药中的关键作用。
Antimicrob Agents Chemother. 2013 Jul;57(7):2972-80. doi: 10.1128/AAC.00140-13. Epub 2013 Apr 15.
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Efficacy of bacteriophage treatment on Pseudomonas aeruginosa biofilms.噬菌体治疗对铜绿假单胞菌生物膜的疗效。
J Endod. 2013 Mar;39(3):364-9. doi: 10.1016/j.joen.2012.10.023. Epub 2012 Nov 28.
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Phage-antibiotic synergism: a possible approach to combatting Pseudomonas aeruginosa.噬菌体-抗生素协同作用:一种对抗铜绿假单胞菌的可能方法。
Res Microbiol. 2013 Jan;164(1):55-60. doi: 10.1016/j.resmic.2012.08.008. Epub 2012 Sep 7.
7
Synergistic phage-antibiotic combinations for the control of Escherichia coli biofilms in vitro.用于体外控制大肠杆菌生物膜的协同噬菌体 - 抗生素组合
FEMS Immunol Med Microbiol. 2012 Jul;65(2):395-8. doi: 10.1111/j.1574-695X.2012.00977.x. Epub 2012 May 18.
8
Diffusion of bacteriophages through artificial biofilm models.噬菌体在人工生物膜模型中的扩散。
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9
Genomic analysis and relatedness of P2-like phages of the Burkholderia cepacia complex.伯克霍尔德氏菌复合群 P2 样噬菌体的基因组分析及其亲缘关系。
BMC Genomics. 2010 Oct 25;11:599. doi: 10.1186/1471-2164-11-599.
10
Burkholderia cenocepacia in cystic fibrosis: epidemiology and molecular mechanisms of virulence.西地西菌属在囊性纤维化中的作用:流行病学和毒力的分子机制。
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洋葱伯克霍尔德菌复合体的噬菌体 - 抗生素协同作用(PAS):抗生素刺激溶菌噬菌体活性。

Burkholderia cepacia complex Phage-Antibiotic Synergy (PAS): antibiotics stimulate lytic phage activity.

作者信息

Kamal Fatima, Dennis Jonathan J

机构信息

Centennial Centre for Interdisciplinary Science, Department of Biological Sciences, University of Alberta, Edmonton, Alberta, Canada.

Centennial Centre for Interdisciplinary Science, Department of Biological Sciences, University of Alberta, Edmonton, Alberta, Canada

出版信息

Appl Environ Microbiol. 2015 Feb;81(3):1132-8. doi: 10.1128/AEM.02850-14. Epub 2014 Dec 1.

DOI:10.1128/AEM.02850-14
PMID:25452284
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4292504/
Abstract

The Burkholderia cepacia complex (Bcc) is a group of at least 18 species of Gram-negative opportunistic pathogens that can cause chronic lung infection in cystic fibrosis (CF) patients. Bcc organisms possess high levels of innate antimicrobial resistance, and alternative therapeutic strategies are urgently needed. One proposed alternative treatment is phage therapy, the therapeutic application of bacterial viruses (or bacteriophages). Recently, some phages have been observed to form larger plaques in the presence of sublethal concentrations of certain antibiotics; this effect has been termed phage-antibiotic synergy (PAS). Those reports suggest that some antibiotics stimulate increased production of phages under certain conditions. The aim of this study is to examine PAS in phages that infect Burkholderia cenocepacia strains C6433 and K56-2. Bcc phages KS12 and KS14 were tested for PAS, using 6 antibiotics representing 4 different drug classes. Of the antibiotics tested, the most pronounced effects were observed for meropenem, ciprofloxacin, and tetracycline. When grown with subinhibitory concentrations of these three antibiotics, cells developed a chain-like arrangement, an elongated morphology, and a clustered arrangement, respectively. When treated with progressively higher antibiotic concentrations, both the sizes of plaques and phage titers increased, up to a maximum. B. cenocepacia K56-2-infected Galleria mellonella larvae treated with phage KS12 and low-dose meropenem demonstrated increased survival over controls treated with KS12 or antibiotic alone. These results suggest that antibiotics can be combined with phages to stimulate increased phage production and/or activity and thus improve the efficacy of bacterial killing.

摘要

洋葱伯克霍尔德菌复合体(Bcc)是一组至少由18种革兰氏阴性机会致病菌组成的菌群,可在囊性纤维化(CF)患者中引起慢性肺部感染。Bcc微生物具有高度的固有抗菌抗性,因此迫切需要替代治疗策略。一种提议的替代治疗方法是噬菌体疗法,即细菌病毒(或噬菌体)的治疗性应用。最近,有人观察到一些噬菌体在亚致死浓度的某些抗生素存在下会形成更大的噬菌斑;这种效应被称为噬菌体 - 抗生素协同作用(PAS)。这些报告表明,某些抗生素在特定条件下会刺激噬菌体产量增加。本研究的目的是检测感染洋葱伯克霍尔德菌C6433和K56 - 菌株的噬菌体中的PAS。使用代表4种不同药物类别的6种抗生素对Bcc噬菌体KS12和KS14进行PAS测试。在所测试的抗生素中,美罗培南、环丙沙星和四环素的效果最为显著。当与这三种抗生素的亚抑制浓度一起培养时,细胞分别呈现出链状排列、细长形态和聚集排列。当用逐渐增加的抗生素浓度处理时,噬菌斑大小和噬菌体滴度均增加,直至达到最大值。用噬菌体KS12和低剂量美罗培南处理感染洋葱伯克霍尔德菌K56 - 2的大蜡螟幼虫,其存活率高于单独用KS12或抗生素处理的对照组。这些结果表明,抗生素可与噬菌体联合使用,以刺激噬菌体产量增加和/或活性增强,从而提高细菌杀灭效果。