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光催化TiO纳米颗粒和裂解性噬菌体vb_EcoS_bov25_1D对肠出血性大肠杆菌O157:H7 Sakai菌株的抗菌效果干扰

Antibacterial efficacy interference of the photocatalytic TiO nanoparticle and the lytic bacteriophage vb_EcoS_bov25_1D on the Enterohaemorragic strain Sakai.

作者信息

Steinbach Anita, Sváb Domonkos, Kőrösi László, Kerényi Monika, Kun József, Urbán Péter, Palkovics Tamás, Kovács Tamás, György Schneider

机构信息

Department of Medical Microbiology and Immunology, Medical School, University of Pécs, 7624, Pécs, Hungary.

HUN-REN Veterinary Medical Research Institute, 1143, Budapest, Hungary.

出版信息

Heliyon. 2024 Jun 27;10(14):e33562. doi: 10.1016/j.heliyon.2024.e33562. eCollection 2024 Jul 30.

DOI:10.1016/j.heliyon.2024.e33562
PMID:39108916
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11301168/
Abstract

Post-antibiotic era requires the use of alternative pesticides against bacterial infections. One potential application field is agriculture, where pesticides are routinely applied in combinations. In this study we tested the interference of antibacterial effects of two alternative antimicrobials with basically different mode of actions if applied together by using the Enterohemorrhagic strain Sakai as a modelorganism, one strain of a pathotype that is frequently associated with meat and plant derived infections. TiO is a photocatalytically active nanomaterial, which can generate reactive oxygen species (ROS), exerting destructive effects on macromolecules, while the vb_EcoS_bov25_1D bacteriophage has a specific lytic action. Both, bacteriophages and Sakai were sensitive against ROS if tested separately, during that PFUs of bacteriophages dropped from 5 × 10 to 0 in 4 h, while in case of Sakai CFUs decreased with 5 and 2 logs of magnitude in the presence of 0,05 % and 0,025 % of TiO respectively. In Sakai by the sixth minute of ROS exposition the expressions of superoxide dismutases and catalases were boosted, as revealed by whole transcriptomic analyses, but the elevated levels and support some roles of these genes under this stress situation. Combined application of phages and TiO under UV-A exposure have revealed that beside the inner enzymatic defence mechanisms presenting phage particles served as shields and spoiled the antimicrobial effect of TiO (0,0125 %). As a consequence, phages became sacrificed as during exposition a 3-log drop (5 × 10→5 × 10) in their PFUs was revealed. Survived bacteriophages however in the system remained active and under the subsequent dark phase the 3-log drop in the PFU was compensated in 24 h. Our results show that joint application of the two alternative antimicrobial agents TiO and a bacteriophage can have two consequences depending on the circumstances they were used. From one side they complement each other's effects in that TiO can exert its effect on UV-A or sunlight exposed areas, whereas the bacteriophage on non-exposed surfaces. On the other hand, they also can spoil each others effect as phages can bind generated ROS and by that protect target bacteria, but bacteria themselves can serve as shields and by that protect phages from the destroying effect of ROS, phages however can exert their antibacterial effects on bacteria.

摘要

抗生素后时代需要使用替代农药来对抗细菌感染。一个潜在的应用领域是农业,在农业中农药通常是混合使用的。在本研究中,我们以肠出血性大肠杆菌阪崎菌株作为模式生物,测试了两种作用方式基本不同的替代抗菌剂共同使用时的抗菌效果干扰情况,该菌株是一种经常与肉类和植物源性感染相关的致病型菌株。二氧化钛(TiO)是一种具有光催化活性的纳米材料,可产生活性氧(ROS),对大分子产生破坏作用,而vb_EcoS_bov25_1D噬菌体具有特异性裂解作用。如果分别进行测试,噬菌体和阪崎菌株对ROS均敏感,在此期间,噬菌体的噬菌斑形成单位(PFU)在4小时内从5×10降至0,而对于阪崎菌株,在分别存在0.05%和0.025%的TiO时,其菌落形成单位(CFU)分别下降了5个和2个数量级。通过全转录组分析发现,在阪崎菌株中,ROS暴露6分钟后,超氧化物歧化酶和过氧化氢酶的表达增强,但这些基因在这种应激情况下的高水平表达支持了它们的一些作用。在紫外线A照射下联合应用噬菌体和TiO表明,除了内部酶防御机制外,噬菌体颗粒起到了屏蔽作用,破坏了TiO(0.0125%)的抗菌效果。结果,噬菌体被牺牲,因为在暴露过程中其PFU下降了3个对数(5×10→5×10)。然而,系统中存活的噬菌体仍然具有活性,在随后的黑暗阶段,PFU的3个对数下降在24小时内得到了补偿。我们的结果表明,两种替代抗菌剂TiO和噬菌体的联合应用根据使用的情况可能会产生两种结果。一方面,它们相互补充作用,因为TiO可对紫外线A或阳光照射区域发挥作用,而噬菌体则对未暴露表面发挥作用。另一方面,它们也可能相互破坏作用,因为噬菌体可以结合产生的ROS从而保护目标细菌,但细菌本身也可以起到屏蔽作用,从而保护噬菌体免受ROS的破坏作用,不过噬菌体可以对细菌发挥抗菌作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/103f/11301168/129f921891ab/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/103f/11301168/c7d81a803667/gr1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/103f/11301168/3558a43d552e/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/103f/11301168/1af355a4cd37/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/103f/11301168/129f921891ab/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/103f/11301168/c7d81a803667/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/103f/11301168/917ff0e2fb9d/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/103f/11301168/3558a43d552e/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/103f/11301168/1af355a4cd37/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/103f/11301168/129f921891ab/gr5.jpg

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