抗细菌
抗菌肽
结核分枝杆菌
抗菌剂
肺结核
生物
细胞毒性
抗生素
微生物学
先天免疫系统
体外
免疫系统
生物化学
免疫学
医学
病理
作者
Ning Yu,Lujuan Wang,Menglu Wang,Xiangying Meng,Jinjuan Qiao
出处
期刊:Protein and Peptide Letters
[Bentham Science Publishers]
日期:2023-03-16
卷期号:30 (4): 280-294
被引量:5
标识
DOI:10.2174/0929866530666230315113624
摘要
Abstract: The high global burden of tuberculosis (TB) and the increasing emergence of the drugresistant (DR) strain of Mycobacterium tuberculosis (Mtb) emphasize the urgent need for novel antimycobacterial agents. Antimicrobial peptides (AMPs) are small peptides widely existing in a variety of organisms and usually have amphiphilic cationic structures, which have a selective affinity to the negatively charged bacterial cell wall. Besides direct bactericidal mechanisms, including interacting with the bacterial cell membrane and interfering with the biosynthesis of the cell wall, DNA, or protein, some AMPs are involved in the host's innate immunity. AMPs are promising alternative or complementary agents for the treatment of DR-TB, given their various antibacterial mechanisms and low cytotoxicity. A large number of AMPs, synthetic or natural, from human to bacteriophage sources, have displayed potent anti-mycobacterial activity in vitro and in vivo. In this review, we summarized the features, antimycobacterial activity, and mechanisms of action of the AMPs according to their sources. Although AMPs have not yet met the expectations for clinical application due to their low bioavailabilities, high cost, and difficulties in large-scale production, their potent antimycobacterial activity and action mechanisms, which are different from conventional antibiotics, make them promising antibacterial agents against DR-Mtb in the future.
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