Development of benzimidazole-based derivatives as antimicrobial agents and their synergistic effect with colistin against gram-negative bacteria

被引:56
作者
Dokla, Eman M. E. [1 ]
Abutaleb, Nader S. [2 ]
Milik, Sandra N. [1 ,3 ]
Li, Daoyi [2 ]
El-Baz, Karim [1 ,4 ,5 ]
Shalaby, Menna-Allah W. [1 ]
Al-Karaki, Rawan [6 ]
Nasr, Maha [7 ]
Klein, Christian D. [3 ]
Abouzid, Khaled A. M. [1 ,8 ]
Seleem, Mohamed N. [2 ,9 ]
机构
[1] Ain Shams Univ, Fac Pharm, Pharmaceut Chem Dept, Cairo 11566, Egypt
[2] Purdue Univ, Coll Vet Med, Dept Comparat Pathobiol, W Lafayette, IN 47907 USA
[3] Heidelberg Univ, Med Chem, IPMB, Neuenheimer Feld 364, D-69120 Heidelberg, Germany
[4] KIST, Brain Sci Inst, Ctr Neuromed, Hwarangro 14 Gil 5, Seoul 136791, South Korea
[5] UST, KIST Sch, Div Biomed Sci & Technol, Gajungro 217, Daejeon 305350, South Korea
[6] Mutah Univ, Fac Pharm, Dept Pharmaceut & Pharmaceut Technol, Al Karak 61710, Jordan
[7] Ain Shams Univ, Fac Pharm, Dept Pharmaceut & Ind Pharm, Cairo 11566, Egypt
[8] Univ Sadat City, Fac Pharm, Dept Organ & Med Chem, Sadat City 32897, Egypt
[9] Purdue Inst Inflammat Immunol & Infect Dis, W Lafayette, IN 47907 USA
关键词
Benzimidazole; Gram-negative bacteria; Phenotypic screening; Antimicrobial resistance; Antibiotic synergy; ESCHERICHIA-COLI; RESISTANCE; PERMEABILITY; LIGANDS; POTENT;
D O I
10.1016/j.ejmech.2019.111850
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Gram-negative bacteria pose a distinctive risk worldwide, especially with the evolution of major resistance to carbapenems, fluoroquinolones and colistin. Therefore, development of new antibacterial agents to target Gram-negative infections is of utmost importance. Using phenotypic screening, we synthesized and tested thirty-one benzimidazole derivatives against E. coli JW55031 (TolC mutant strain). Compound 6c showed potent activity with MlC value of 2 mu g/ml, however, it lacked activity against several Gram-negative microbes with intact efflux systems, including E. coli BW25113 (wild-type strain). Combination of 6c with colistin partially restored its antibacterial activity against wild strains (MlC range, 8-16 mu g/ml against E. coli, K. pneumoniae, A. baumannii, and P. aeruginosa). 6c exhibited no cytotoxicity against two mammalian cell lines. Therefore, compound 6c represents a promising lead for further optimization to overcome Gram-negative resistance alone or in combination therapy. (C) 2019 Elsevier Masson SAS. All rights reserved.
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页数:9
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