非抗生素药物对铜绿假单胞菌TGC04定植作用的初步认识

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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引用次数: 0

摘要

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