Departamento de Biologia Celular e Molecular, Laboratório de Antibióticos, Bioquímica e Modelagem Molecular (LABioMol), Instituto de Biologia, CEG, Universidade Federal Fluminense, CEP 24001-970, Niterói, Brazil.
Evid Based Complement Alternat Med. 2011;2011:960267. doi: 10.1093/ecam/nen052. Epub 2011 Jun 5.
Bacterial infections involving multidrug-resistant strains are one of the ten leading causes of death and an important health problem in need for new antibacterial sources and agents. Herein, we tested and compared four snake venoms (Agkistrodon rhodostoma, Bothrops jararaca, B. atrox and Lachesis muta) against 10 Gram-positive and Gram-negative drug-resistant clinical bacteria strains to identify them as new sources of potential antibacterial molecules. Our data revealed that, as efficient as some antibiotics currently on the market (minimal inhibitory concentration (MIC) = 1-32 μg mL(-1)), A. rhodostoma and B. atrox venoms were active against Staphylococcus epidermidis and Enterococcus faecalis (MIC = 4.5 μg mL(-1)), while B. jararaca inhibited S. aureus growth (MIC = 13 μg ml(-1)). As genomic and proteomic technologies are improving and developing rapidly, our results suggested that A. rhodostoma, B. atrox and B. jararaca venoms and glands are feasible sources for searching antimicrobial prototypes for future design new antibiotics against drug-resistant clinical bacteria. They also point to an additional perspective to fully identify the pharmacological potential of these venoms by using different techniques.
细菌感染涉及多药耐药菌株是十大死亡原因之一,也是一个需要新的抗菌来源和药物的重要健康问题。在此,我们测试并比较了四种蛇毒(蝮蛇、矛头蝮、矛头蝮和矛头蝮)对 10 种革兰氏阳性和革兰氏阴性耐药临床细菌株的作用,以确定它们是具有潜在抗菌分子的新来源。我们的数据表明,与目前市场上的一些抗生素一样有效(最小抑菌浓度(MIC)= 1-32 μg mL(-1)),蝮蛇和矛头蝮蛇毒对表皮葡萄球菌和粪肠球菌具有活性(MIC = 4.5 μg mL(-1)),而矛头蝮蛇毒抑制金黄色葡萄球菌生长(MIC = 13 μg ml(-1))。随着基因组和蛋白质组技术的不断改进和快速发展,我们的结果表明,蝮蛇、矛头蝮蛇和矛头蝮蛇毒和腺体是寻找针对耐药临床细菌的新型抗生素的抗菌原型的可行来源。它们还为充分利用这些毒液的药理潜力提供了一个额外的视角,通过使用不同的技术。