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温和噬菌体介导抑制细菌群运动性的抗菌效果。

Antibacterial efficacy of temperate phage-mediated inhibition of bacterial group motilities.

机构信息

Department of Pharmacy, College of Pharmacy, CHA University, Seongnam, Gyeonggi-do, South Korea.

出版信息

Antimicrob Agents Chemother. 2012 Nov;56(11):5612-7. doi: 10.1128/AAC.00504-12. Epub 2012 Aug 20.

Abstract

Phage therapy against bacterial pathogens has been resurrected as an alternative and supplementary anti-infective modality. Here, we observed that bacterial group motilities were impaired in Pseudomonas aeruginosa strain PA14 lysogens for some temperate siphophages; the PA14 lysogens for DMS3 and MP22 were impaired in swarming motility, whereas the PA14 lysogen for D3112 was impaired in twitching motility. The swarming and twitching motilities of PA14 were also affected in the presence of MP22 and D3112, respectively. The in vitro killing activities of D3112 and MP22 toward PA14 did not differ, and neither did their in vivo persistence in the absence of bacterial infections in mice as well as in flies. Nevertheless, administration of D3112, not MP22, significantly reduced the mortality and the bacterial burdens in murine peritonitis-sepsis and Drosophila systemic infection caused by PA14. Taken together, we suggest that a temperate phage-mediated twitching motility inhibition might be comparably effective to control the acute infections caused by P. aeruginosa.

摘要

噬菌体治疗对抗细菌病原体的方法已经复活,成为一种替代和补充的抗感染手段。在这里,我们观察到一些温和噬菌体的溶源性细菌群体的运动能力受损;DMS3 和 MP22 的 PA14 溶源菌在群体运动中受损,而 D3112 的 PA14 溶源菌在蠕动运动中受损。MP22 和 D3112 的存在也分别影响了 PA14 的群集运动和抽动运动。D3112 和 MP22 对 PA14 的体外杀伤活性没有差异,而且在没有细菌感染的情况下,它们在小鼠和苍蝇体内的持久性也没有差异。然而,给予 D3112 而不是 MP22 可显著降低由 PA14 引起的小鼠腹膜炎-败血症和 Drosophila 全身感染的死亡率和细菌负荷。综上所述,我们认为温和噬菌体介导的抽动运动抑制可能与控制由铜绿假单胞菌引起的急性感染同样有效。

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