Post-graduate Program in Pharmaceutical Sciences, School of Pharmacy, Dentistry and Nursing, Federal University of Ceará, Fortaleza, CE, Brazil.
Center for Science and Technology, State University of Ceará, Fortaleza, CE, Brazil.
Toxicon. 2020 Nov;187:19-28. doi: 10.1016/j.toxicon.2020.08.015. Epub 2020 Aug 27.
The predatory giant ant Dinoponera quadriceps is one of the largest venomous ants on Earth. The venom of D. quadriceps comprises a rich blend of bioactive peptides that includes structures related to at least five classes of antimicrobial peptides. In the present study, two representative synthetic peptides, sDq-2562 and sDq-3162, belonging to the ponericin-like dinoponeratoxin family, were evaluated for their microbicide activity against antibiotic-resistant bacteria. The most effective peptide, the 28-residue sDq-3162 displayed a significant bacteriostatic and bactericidal effect with minimal inhibitory concentrations (MICs) between 5 μM and 10 μM (15.6 μg mL and 31.2 μg mL), according to the strain of drug-resistant bacteria tested. In combination with conventional antibiotics, sDq-3162 displayed in vitro synergistic effects, reducing the MICs of antibiotics for more than 2-log against clinical isolates of carbapenem-resistant Acinetobacter baumannii, Klebsiella pneumoniae and Pseudomonas aeruginosa, with low cytotoxicity to human erythrocytes, in vitro. Since the development of molecules to circumvent the spread of antibiotic-resistant bacteria is demanding, ant venom peptides arise as useful molecular resources to contribute with the antimicrobial arsenal and therapeutic strategies to fight clinically relevant microbial infections.
掠食性巨型蚂蚁 Dinoponera quadriceps 是地球上最大的毒蚂蚁之一。D. quadriceps 的毒液包含丰富的生物活性肽混合物,其中包括至少与五类抗菌肽相关的结构。在本研究中,两种代表性的合成肽,sDq-2562 和 sDq-3162,属于 ponerin 样 dinoponeratoxin 家族,被评估其对具有抗药性的细菌的抗微生物活性。最有效的肽,28 个残基的 sDq-3162 对不同的抗药性细菌菌株显示出显著的抑菌和杀菌作用,最小抑菌浓度(MIC)在 5 μM 和 10 μM 之间(15.6 μg mL 和 31.2 μg mL)。根据体外实验,sDq-3162 与常规抗生素联合使用显示出协同作用,将抗生素的 MIC 值降低了超过 2 个对数级,对耐碳青霉烯类的鲍曼不动杆菌、肺炎克雷伯菌和铜绿假单胞菌的临床分离株有效,同时对人红细胞的细胞毒性很低。由于开发分子来规避抗药性细菌的传播具有挑战性,因此抗毒液肽作为有用的分子资源,有助于对抗临床上相关的微生物感染的抗菌武器和治疗策略。