利用渗透休克和苯扎氯铵从噬菌体中生产泰洛菌素。

PHAGE (New Rochelle, N.Y.) Pub Date : 2023-09-01 Epub Date: 2023-09-20 DOI:10.1089/phage.2023.0014
Cedric Woudstra, Lone Brøndsted
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引用次数: 1

摘要

鉴于全球抗生素耐药性危机,迫切需要新的抗生素替代品。细菌为环境竞争而产生的泰洛菌素或噬菌体尾巴状细菌素颗粒是抗生素治疗的潜在抗菌替代品。然而,具有特征的泰洛星的可用性是有限的。我们探索了用渗透休克或季铵化合物苯扎氯铵对阿克曼病毒科噬菌体S117进行化学处理,并用Straboviridae噬菌体T4作为对照,从噬菌体颗粒中生产新的泰洛菌素的可能性。我们报道了噬菌体S117对这种处理具有抗性,而噬菌体T4通过渗透休克成功生产泰洛菌素。最后,用苯扎氯铵的化学处理对噬菌体S117无效,但成功地灭活了噬菌体T4而不产生泰洛菌素。需要进一步的研究来实现对噬菌体的这种处理,以产生具有杀伤活性的泰洛菌素。
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Producing Tailocins from Phages Using Osmotic Shock and Benzalkonium Chloride.

In the light of the worldwide antimicrobial resistance crisis, new substitutes to antibiotics are urgently needed. Tailocins or phage tail-like bacteriocin particles, produced by bacteria for environmental competition, are a potential antimicrobial alternative to antibiotic treatment. Yet, the availability of characterized Tailocins is limited. We explored the possibility to produce new Tailocins from phage particles, using osmotic shock or chemical treatment by the ammonium quaternary compound benzalkonium chloride on Ackermannviridae phage S117 and using Straboviridae phage T4 as control. We report that phage S117 was resistant to such treatment, while successful production of Tailocins by osmotic shock was achieved for phage T4. Finally, chemical treatment with benzalkonium chloride was inefficient on phage S117 but successfully inactivated phage T4 without production of Tailocins. Further studies are needed to implement such treatments of phages for producing Tailocins with killing activity.

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