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仅使用精氨酸和联苯丙氨酸设计的超短抗菌肽UP-5的抗菌及抗生物膜活性

Antimicrobial and Antibiofilm Activity of UP-5, an Ultrashort Antimicrobial Peptide Designed Using Only Arginine and Biphenylalanine.

作者信息

Almaaytah Ammar, Qaoud Mohammed T, Khalil Mohammed Gubran, Abualhaijaa Ahmad, Knappe Daniel, Hoffmann Ralf, Al-Balas Qosay

机构信息

Department of Pharmaceutical Technology, Faculty of Pharmacy, Jordan University of Science and Technology, Irbid 22110, Jordan.

Department of Applied Biological Sciences, Faculty of Science and Arts, Jordan University of Science and Technology, Irbid 22110 Jordan.

出版信息

Pharmaceuticals (Basel). 2018 Jan 2;11(1):3. doi: 10.3390/ph11010003.

Abstract

The recent upsurge of multidrug resistant bacteria (MDRB) among global communities has become one of the most serious challenges facing health professionals and the human population worldwide. Cationic ultrashort antimicrobial peptides (USAMPs) are a promising group of molecules that meet the required criteria of novel antimicrobial drug development. UP-5, a novel penta-peptide, displayed significant antimicrobial activities against various standard and clinical isolates of MDRB. UP-5 displayed MICs values within the range of (10-15 μM) and (55-65 μM) against Gram-positive and Gram-negative bacteria, respectively. Furthermore, UP-5 displayed antibiofilm activity with minimum biofilm eradication concentration (MBEC) value as equal to twofold higher than MIC value. At the same inhibitory concentrations, UP-5 exhibited very low or negligible toxicity toward human erythrocytes and mammalian cells. Combining UP-5 with conventional antibiotics led to a synergistic or additive mode of action that resulted in the reduction of the MIC values for some of the antibiotics by 99.7% along a significant drop in MIC values of the peptide. The stability profile of UP-5 was evaluated in full mouse plasma and serum with results indicating a more stable pattern in plasma. The present study indicates that USAMPs are promising antimicrobial agents that can avoid the negative characteristics of conventional antimicrobial peptides. Additionally, USAMPs exhibit good to moderate activity against MDRB, negligible toxicity, and synergistic outcomes in combination with conventional antimicrobial agents.

摘要

全球范围内多重耐药菌(MDRB)的近期激增已成为全球卫生专业人员和人类面临的最严峻挑战之一。阳离子超短抗菌肽(USAMPs)是一类有前景的分子,符合新型抗菌药物开发的要求标准。新型五肽UP-5对多种标准菌株和临床分离的MDRB表现出显著的抗菌活性。UP-5对革兰氏阳性菌和革兰氏阴性菌的最低抑菌浓度(MIC)值分别在(10 - 15 μM)和(55 - 65 μM)范围内。此外,UP-5表现出抗生物膜活性,其最低生物膜清除浓度(MBEC)值比MIC值高两倍。在相同的抑制浓度下,UP-5对人红细胞和哺乳动物细胞表现出极低或可忽略不计的毒性。将UP-5与传统抗生素联合使用导致协同或相加作用模式,使一些抗生素的MIC值降低了99.7%,同时该肽的MIC值也显著下降。在全小鼠血浆和血清中评估了UP-5的稳定性,结果表明其在血浆中的模式更稳定。本研究表明,USAMPs是有前景的抗菌剂,可避免传统抗菌肽的负面特性。此外,USAMPs对MDRB表现出良好至中等的活性、可忽略不计的毒性以及与传统抗菌剂联合使用时的协同效果。

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