Raza Sada, Bończak Bartłomiej, Atamas Nataliia, Karpińska Aneta, Ratajczyk Tomasz, Łoś Marcin, Hołyst Robert, Paczesny Jan
Institute of Physical Chemistry, Polish Academy of Sciences, Kasprzaka 44/52, 01-224, Warsaw, Poland.
Taras Shevchenko National University of Kyiv, Hlushkova Avenue 4, Kiev, 03127, Ukraine.
Appl Microbiol Biotechnol. 2025 Jan 25;109(1):24. doi: 10.1007/s00253-025-13414-4.
Bacteriophage infections in bacterial cultures pose a significant challenge to industrial bioprocesses, necessitating the development of innovative antiphage solutions. This study explores the antiphage potential of indigo carmine (IC), a common FDA-approved food additive. IC demonstrated selective inactivation of DNA phages (P001, T4, T1, T7, λ) with the EC values ranging from 0.105 to 0.006 mg/mL while showing no activity against the RNA phage MS2. Fluorescence correlation spectroscopy (FCS) revealed that IC selectively binds to dsDNA, demonstrated by a significant reduction in the diffusion coefficient, whereas no binding was observed with ssDNA or RNA. Mechanistically, IC permeates the phage capsid, leading to genome ejection and capsid deformation, as confirmed by TEM imaging. Under optimal conditions (50 °C, 220 rpm), IC achieved up to a 7-log reduction in phage titer, with kinetic theory supporting the enhanced collision frequency induced by agitation. Additionally, IC protected E. coli cultures from phage-induced lysis without affecting bacterial growth or protein production, as demonstrated by GFP expression assays. IC's effectiveness and environmental safety, combined with its FDA approval and cost-effectiveness, make it a promising antiphage agent for industrial applications. KEY POINTS: • Indigo carmine effectively inactivates a broad spectrum of bacteriophages, offering protection to bacteria in industrial cultures. • A novel application of indigo carmine as a food-grade, environmentally safe, and FDA-approved antiphage agent protecting bacterial cultures. • Antiphage activity arises from indigo carmine's interaction with DNA within the phage capsid without harming bacterial cells or compromising protein production in bacterial cultures.
细菌培养物中的噬菌体感染对工业生物过程构成了重大挑战,因此需要开发创新的抗噬菌体解决方案。本研究探索了靛蓝胭脂红(IC)的抗噬菌体潜力,IC是一种常见的经美国食品药品监督管理局(FDA)批准的食品添加剂。IC对DNA噬菌体(P001、T4、T1、T7、λ)表现出选择性灭活作用,其半数有效浓度(EC)值范围为0.105至0.006mg/mL,而对RNA噬菌体MS2无活性。荧光相关光谱法(FCS)显示,IC选择性地与双链DNA结合,这表现为扩散系数显著降低,而与单链DNA或RNA未观察到结合。从机制上讲,IC渗透到噬菌体衣壳中,导致基因组排出和衣壳变形,这通过透射电子显微镜(TEM)成像得到证实。在最佳条件(50°C,220转/分钟)下,IC使噬菌体滴度降低了多达7个对数,动力学理论支持搅拌引起的碰撞频率增加。此外,如绿色荧光蛋白(GFP)表达分析所示,IC保护大肠杆菌培养物免受噬菌体诱导的裂解,而不影响细菌生长或蛋白质生产。IC的有效性和环境安全性,再加上其FDA批准和成本效益,使其成为工业应用中一种有前景的抗噬菌体剂。要点:• 靛蓝胭脂红有效地灭活多种噬菌体,为工业培养中的细菌提供保护。• 靛蓝胭脂红作为一种食品级、环境安全且经FDA批准的抗噬菌体剂保护细菌培养物的新应用。• 抗噬菌体活性源于靛蓝胭脂红与噬菌体衣壳内DNA的相互作用,而不会损害细菌细胞或影响细菌培养物中的蛋白质生产。