Functional Characterization of a Novel Hybrid Peptide with High Potency against Gram-negative Bacteria

被引:5
|
作者
Al Tall, Yara [1 ]
Al-Rawashdeh, Baha'a [3 ]
Abualhaijaa, Ahmad [1 ]
Almaaytah, Ammar [1 ,2 ]
Masadeh, Majed [1 ]
Alzoubi, Karem H. [4 ]
机构
[1] Jordan Univ Sci & Technol, Fac Pharm, Dept Pharmaceut Technol, POB 3030, Irbid 22110, Jordan
[2] Middle East Univ, Fac Pharm, Dept Pharm, Amman, Jordan
[3] Jordan Univ Sci & Technol, Fac Med, Dept Toxicol & Forens Sci, Irbid 22110, Jordan
[4] Jordan Univ Sci & Technol, Fac Pharm, Dept Clin Pharm, Irbid 22110, Jordan
关键词
Antimicrobial peptides; hybridization; resistance; antibiotic adjuvant; synergism; BMR-1; ANTIMICROBIAL PEPTIDE; RESISTANCE; COMBINATION; DRUG; ANTIBIOTICS; PROTEIN; INFECTIONS; MECHANISMS; COMMUNITY;
D O I
10.2174/1381612826666200128090700
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Multi-drug resistant infections are a growing worldwide health concern. There is an urgent need to produce alternative antimicrobial agents. Objective: The study aimed to design a new hybrid antimicrobial peptide, and to evaluate its antimicrobial activity alone and in combination with traditional antibiotics. Methods: Herein, we designed a novel hybrid peptide (BMR-1) using the primary sequences of the parent peptides Frog Esculentin-1a and Monkey Rhesus cathelicidin (RL-37). The positive net charge was increased, and other physicochemical parameters were optimized. The antimicrobial activities of BMR-1 were tested against control and multi-drug resistant gram-negative bacteria. Results: BMR-1 adopted a bactericidal behavior with MIC values of 25-30 mu M. These values reduced by over 75% upon combination with conventional antibiotics (levofloxacin, chloramphenicol, ampicillin, and rifampicin). The combination showed strong synergistic activities in most cases and particularly against multi-drug resistance P. aeruginosa and E. coll. BMR-1 showed similar potency against all tested strains regardless of their resistant mechanisms. BMR-1 exhibited no hemolytic effect on human red blood cells with the effective MIC values against the tested strains. Conclusion: BMR-1 hybrid peptide is a promising candidate to treat resistant infectious diseases caused by gram-negative bacteria.
引用
收藏
页码:376 / 385
页数:10
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