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植物化合物与传统抗菌剂对从牛乳腺炎中分离出的 种细菌的协同作用。 (注:原文中“ spp.”表述不完整,翻译时保留原样)

Synergism of Plant Compound With Traditional Antimicrobials Against spp. Isolated From Bovine Mastitis.

作者信息

Maia Natasha L, de Barros Mariana, de Oliveira Leandro L, Cardoso Silvia A, Dos Santos Marcelo H, Pieri Fabio A, Ramalho Teodorico C, da Cunha Elaine F F, Moreira Maria A S

机构信息

Bacterial Disease Laboratory, Department of Veterinary, Universidade Federal de Viçosa, Viçosa, Brazil.

Immunochemistry and Glycobiology Laboratory, Department of General Biology, Universidade Federal de Viçosa, Viçosa, Brazil.

出版信息

Front Microbiol. 2018 Jun 6;9:1203. doi: 10.3389/fmicb.2018.01203. eCollection 2018.

Abstract

Mastitis is an inflammation of the mammary gland that causes major losses in the dairy industry. spp. are among the main agents of this disease. Increased resistance to antibiotics is one of the causes of therapeutic failure. Plants, due to their broad chemodiversity, are an interesting source of new molecules with antibacterial activity. Using these compounds along with traditional antibiotics is a possible method for reversing resistance. The objective of this work was to determine the interactions between the activities of guttiferone-A and 7-epiclusianone, two active substances isolated from the fruits of , and traditional antibiotics against spp. isolated from bovine mastitis and known to be resistant to them. First, the MIC for the antibiotics and bioactive compounds was determined, followed by their activities, alone and in combination. Then, their cytotoxicity was measured in bovine mammary epithelial cells. Finally, molecular docking simulations were performed to elucidate molecular details of the interactions between β-lactamase and the compounds binding to it (clavulanic acid, ampicillin, 7-epiclusianone, and guttiferone-A). The bacterial isolates were resistant to ampicillin and gentamicin. Both antibiotics showed predominantly synergistic antibacterial activities in combination with guttiferone-A or 7-epiclusianone. These two active substances were not cytotoxic at synergistic concentrations and both showed strong binding to β-lactamase, which may explain the reversal of ampicillin resistance. These substances are promising for the treatment of bovine mastitis.

摘要

乳腺炎是乳腺的一种炎症,会给乳制品行业造成重大损失。 spp.是这种疾病的主要病原体之一。对抗生素耐药性的增加是治疗失败的原因之一。植物因其广泛的化学多样性,是具有抗菌活性的新分子的有趣来源。将这些化合物与传统抗生素一起使用是逆转耐药性的一种可能方法。这项工作的目的是确定从 的果实中分离出的两种活性物质——藤黄双黄酮-A和7-表clusianone与传统抗生素对从牛乳腺炎中分离出且已知对其耐药的 spp.的活性之间的相互作用。首先,确定抗生素和生物活性化合物的最低抑菌浓度(MIC),然后分别及联合测定它们的活性。接着,在牛乳腺上皮细胞中测量它们的细胞毒性。最后,进行分子对接模拟以阐明β-内酰胺酶与与其结合的化合物(克拉维酸、氨苄西林、7-表clusianone和藤黄双黄酮-A)之间相互作用的分子细节。细菌分离株对氨苄西林和庆大霉素耐药。这两种抗生素与藤黄双黄酮-A或7-表clusianone联合使用时主要表现出协同抗菌活性。这两种活性物质在协同浓度下无细胞毒性,且都显示出与β-内酰胺酶有强烈结合,这可能解释了氨苄西林耐药性的逆转。这些物质有望用于治疗牛乳腺炎。

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