Preliminary insights into the action of non-antibiotic pharmaceuticals in the colonization of Pseudomonas aeruginosa TGC04

Mazen Wahib Mohamed Abdelhadi, João Antônio Carvalho Bandeira, L. Pragana, Victor Targino Gomes, Jéssica Vieira Dantas, José Gabriel Santos de Almeida, R. A. Travassos, U. Vasconcelos
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Abstract

Molecules with antimicrobial properties, such as those found in non-antibiotic pharmaceuticals, may pressure bacteria to adapt to the environment. In this work, five of the most sold non-antibiotic pharmaceuticals in Brazil and in Egypt in 2020 (losartan 50 mg, acetylsalicylic acid 100 mg, diclofenac 50 mg, paracetamol 750 mg and metformin 500 mg and dipyrone 100 mg/mL), were tested against the wild strain Pseudomonas aeruginosa TGC04, previously isolated by our group and which has been characterized over the years. We evaluated inhibition of biofilm adhesion over 48 h using the crystal violet test. Exposure of P. aeruginosa TGC04 to the compounds promoted a similar moderate reduction in adherence for all the pharmaceuticals tested, amounting to about 60%. This indicated that the cells were also moderately adherent. However, although all non-antibiotic pharmaceuticals did not produce a biocidal effect on the wild strain, intense antibiofilm activity was observed, except for paracetamol.
非抗生素药物对铜绿假单胞菌TGC04定植作用的初步认识
具有抗菌特性的分子,例如在非抗生素药物中发现的分子,可能会迫使细菌适应环境。在这项工作中,我们对巴西和埃及2020年销量最大的五种非抗生素药物(氯沙坦50 mg,乙酰水杨酸100 mg,双氯芬酸50 mg,对乙酰氨基酚750 mg,二甲双胍500 mg和双吡酮100 mg/mL)进行了抗铜绿假单胞菌TGC04野生菌株的测试,该菌株是我们小组之前分离出来的,并且已经鉴定了多年。我们用结晶紫试验评估了对生物膜粘附的抑制作用超过48小时。铜绿假单胞菌TGC04暴露于这些化合物中,对所有测试药物的依从性也有类似的中度降低,约为60%。这表明细胞也具有中等贴壁性。然而,尽管所有非抗生素药物都没有对野生菌株产生生物杀灭作用,但除了扑热息痛外,还观察到强烈的抗生物膜活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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