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噬菌蛭弧菌和贪噬菌属捕食人类病原体。

Predation of human pathogens by the predatory bacteria Micavibrio aeruginosavorus and Bdellovibrio bacteriovorus.

机构信息

Department of Oral Biology, University of Medicine and Dentistry of New Jersey, Newark, NJ 07101, USA.

出版信息

J Appl Microbiol. 2011 Feb;110(2):431-44. doi: 10.1111/j.1365-2672.2010.04900.x. Epub 2010 Nov 29.

Abstract

AIMS

The focus of this study was to evaluate the potential use of the predatory bacteria Bdellovibrio bacteriovorus and Micavibrio aeruginosavorus to control the pathogens associated with human infection.

METHODS AND RESULTS

By coculturing B. bacteriovorus 109J and M. aeruginosavorus ARL-13 with selected pathogens, we have demonstrated that predatory bacteria are able to attack bacteria from the genus Acinetobacter, Aeromonas, Bordetella, Burkholderia, Citrobacter, Enterobacter, Escherichia, Klebsiella, Listonella, Morganella, Proteus, Pseudomonas, Salmonella, Serratia, Shigella, Vibrio and Yersinia. Predation was measured in single and multispecies microbial cultures as well as on monolayer and multilayer preformed biofilms. Additional experiments aimed at assessing the optimal predation characteristics of M. aeruginosavorus demonstrated that the predator is able to prey at temperatures of 25-37°C but is unable to prey under oxygen-limiting conditions. In addition, an increase in M. aeruginosavorus ARL-13 prey range was also observed.

CONCLUSIONS

Bdellovibrio bacteriovorus and M. aeruginosavorus have an ability to prey and reduce many of the multidrug-resistant pathogens associated with human infection.

SIGNIFICANCE AND IMPACT OF THE STUDY

Infectious complications caused by micro-organisms that have become resistant to drug therapy are an increasing problem in medicine, with more infections becoming difficult to treat using traditional antimicrobial agents. The work presented here highlights the potential use of predatory bacteria as a biological-based agent for eradicating multidrug-resistant bacteria, with the hope of paving the way for future studies in animal models.

摘要

目的

本研究的重点是评估捕食性细菌蛭弧菌和 Aeruginosavorus Micavibrio 控制与人类感染相关病原体的潜在用途。

方法和结果

通过将 109J 型噬菌蛭弧菌和 Aeruginosavorus Micavibrio ARL-13 与选定的病原体共培养,我们证明了捕食性细菌能够攻击不动杆菌属、气单胞菌属、百日咳博德特氏菌属、伯克霍尔德氏菌属、柠檬酸杆菌属、肠杆菌属、大肠杆菌、克雷伯氏菌属、李斯特菌属、摩氏摩根菌属、变形菌属、假单胞菌属、沙门氏菌属、沙雷氏菌属、弧菌属和耶尔森氏菌属的细菌。捕食作用在单种和多种微生物培养物以及单层和多层预制生物膜中进行了测量。旨在评估 Aeruginosavorus Micavibrio 最佳捕食特性的额外实验表明,捕食者能够在 25-37°C 的温度下捕食,但不能在缺氧条件下捕食。此外,还观察到 Aeruginosavorus Micavibrio ARL-13 的捕食范围增加。

结论

蛭弧菌和 Aeruginosavorus Micavibrio 能够捕食并减少许多与人类感染相关的多药耐药病原体。

研究的意义和影响

由于对药物治疗产生耐药性的微生物引起的感染并发症是医学中日益严重的问题,越来越多的感染变得难以用传统的抗菌药物治疗。这里介绍的工作强调了捕食性细菌作为一种基于生物的根除多药耐药细菌的潜在用途,希望为未来的动物模型研究铺平道路。

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