Santos Maria H C, Santos Valdenice F, Freitas Priscilla R, Silva Romério R S, Roma Renato Rodrigues, Santos Ana L E, Ribeiro Daiany Alves, Coutinho Henrique D M, Rocha Bruno A M, Oliveira Manoel M E, Teixeira Claudener S
Agrarian and Environmental Sciences Center, Federal University of Maranhão, Chapadinha, MA, Brazil.
Department of Biological Chemistry, Regional University of Cariri, Crato, CE, Brazil.
Int J Biol Macromol. 2023 May 1;236:123941. doi: 10.1016/j.ijbiomac.2023.123941. Epub 2023 Mar 7.
DVL is a Man/Glc-binding lectin from Dioclea violacea seeds that has the ability to interact with the antibiotic gentamicin. The present work aimed to evaluate whether the DVL has the ability to interact with neomycin via CRD and to examine the ability of this lectin to modulate the antibiotic effect of neomycin against multidrug-resistant strains (MDR). The hemagglutinating activity test revealed that neomycin inhibited the hemagglutinating activity of DVL with a minimum inhibitory concentration of 50 mM, indicating that the antibiotic interacts with DVL via the carbohydrate recognition domain (CRD). DVL immobilized on cyanogen bromide-activated Sepharose® 4B bound 41 % of the total neomycin applied to the column, indicating that the DVL-neomycin interaction is efficient for purification processes. Furthermore, the minimum inhibitory concentrations (MIC) obtained for DVL against all strains studied were not clinically relevant. However, when DVL was combined with neomycin, a significant increase in antibiotic activity was observed against S. aureus and P. aeruginosa. These results demonstrate the first report of lectin-neomycin interaction, indicating that immobilized DVL has the potential to isolate neomycin by affinity chromatography. Moreover, DVL increased the antibiotic activity of neomycin against MDR, suggesting that it is a potent adjuvant in the treatment of infectious diseases.
DVL是一种从紫花蝶豆种子中提取的人/葡萄糖结合凝集素,它能够与抗生素庆大霉素相互作用。本研究旨在评估DVL是否能够通过碳水化合物识别结构域(CRD)与新霉素相互作用,并检验这种凝集素调节新霉素对多重耐药菌株(MDR)抗菌效果的能力。血凝活性测试表明,新霉素抑制DVL的血凝活性,最低抑制浓度为50 mM,这表明抗生素通过碳水化合物识别结构域(CRD)与DVL相互作用。固定在溴化氰活化的琼脂糖凝胶4B上的DVL结合了应用于柱上的41%的新霉素总量,这表明DVL - 新霉素相互作用对纯化过程有效。此外,DVL对所有研究菌株获得的最低抑菌浓度(MIC)在临床上并不相关。然而,当DVL与新霉素联合使用时,观察到对金黄色葡萄球菌和铜绿假单胞菌的抗菌活性显著增加。这些结果首次报道了凝集素 - 新霉素相互作用,表明固定化的DVL具有通过亲和色谱法分离新霉素的潜力。此外,DVL增强了新霉素对多重耐药菌的抗菌活性,表明它是治疗传染病的一种有效佐剂。